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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1224 |
Cefuroxime sodium
Anaptivan,头孢呋辛钠,Cefuroxime sodium salt,Biociclin |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefuroxime sodium (Cefuroxime sodium salt) 是一种具有口服活性的头孢菌素抗生素,增加了对 β-内酰胺酶的稳定性。 | |||
T8507 |
MAC-545496
|
Antibacterial | Microbiology/Virology |
MAC-545496 是一种抗毒剂,可逆转耐甲氧西林的菌株中的 β-内酰胺耐药性。它是糖肽抗性相关蛋白 R 的纳摩尔抑制剂,对全长 GraR 蛋白具有很强的结合亲和力。 | |||
T22269 |
Benzyldodecyldimethylammonium Chloride Dihydrate
|
Antibacterial | Microbiology/Virology |
Benzyldodecyldimethylammonium chloride dihydrate 可以用作杀虫试剂,可以靶向耐药性细菌,如耐甲氧西林金黄色葡萄球菌、耐多药铜绿假单胞菌等,且具有浓度依赖性。 | |||
T19794 |
Temafloxacin
替马沙星,Omniflox |
Antibiotic | Microbiology/Virology |
Temafloxacin (Omniflox) 是一种喹诺酮类广谱抗菌剂,对革兰氏阳性菌、革兰氏阴性菌和厌氧菌均有效。 | |||
T1031 |
Cloxacillin sodium monohydrate
Cloxacillin Sodium,Bactopen,氯唑西林钠一水合物 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cloxacillin sodium monohydrate (Cloxacillin Sodium) 有抗菌作用,对Staphylococcus aureus25923 的最小抑菌浓度为256 mg/L。 | |||
T7804 |
Garenoxacin mesylate hydrate
Garenoxacin mesylate [USAN],加雷沙星甲磺酸盐,BMS284756 (Mesylate hydrate) |
Antibacterial | Microbiology/Virology |
Garenoxacin mesylate hydrate (Garenoxacin mesylate [USAN]) 是一种新型口服 des-fluoro(6) 喹诺酮,具有强抗菌活性,抗呼吸道病原体。 | |||
T1389 |
Dyclonine hydrochloride
盐酸达克罗宁,Dyclocaine hydrochloride,Dyclonine HCl |
Sodium Channel; Antibacterial; Antifungal | Membrane transporter/Ion channel; Microbiology/Virology |
Dyclonine hydrochloride (Dyclonine HCl) 是润喉片的有效成分,具有显著的杀菌和杀真菌作用。 | |||
T1283 |
Clinafloxacin
克林沙星,PD 127391,CI-960,AM-1091 |
Antibacterial; Antibiotic | Microbiology/Virology |
Clinafloxacin (CI-960) 是一种高效广谱氟喹诺酮类抗生素,抑制革兰氏阳性、革兰氏阴性和厌氧病原体。它对金黄色葡萄球菌的 DNA 促旋酶和拓扑异构酶 IV 有抑制作用,IC50值分别为 0.92 µg/ml 和 1.62 µg/ml。 | |||
T0964 |
Floxuridine
氟尿苷,5-Fluorouracil 2'-deoxyriboside,FUDR,Deoxyfluorouridine,NSC 27640 |
Apoptosis; Nucleoside Antimetabolite/Analog; Others; DNA/RNA Synthesis; Antibacterial; HSV | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
Floxuridine (FUDR) 是一种嘧啶类似物,也是一种抗肿瘤代谢物。它抑制胸苷酸合成酶,导致 DNA 合成中断和细胞毒性。它是一种可诱导细胞凋亡的金黄色葡萄球菌感染抑制剂 ,具有抗HSV 和CMV 病毒的作用。 | |||
T7179 |
Garenoxacin
BMS284756,加雷沙星 |
Antibacterial | Microbiology/Virology |
Garenoxacin (BMS284756) 是一种新型的口服 des-fluoro(6) 喹诺酮,有抗菌活性,可抑制呼吸道病原体。 | |||
T1293 |
Gatifloxacin
BMS 206584-01,PD 135432,CG5501,BMS-206584,AM-1155,加替沙星 |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Gatifloxacin (CG5501) 是一种具有广谱抗菌活性的氟喹诺酮类抗生素。它可抑制大肠杆菌 DNA 解旋酶 (IC50=0.109 μg/ml) 和细菌 II 型拓扑异构酶(IC50=13.8 μg/ml)。在动物模型中,它有抗细菌性结膜炎作用。 | |||
T64316 |
VP-4604
1-((4-Nitrophenyl)sulfonyl)piperidine |
Others | Others |
VP-4604是一种有效的抗耐甲氧西林金黄色葡萄球菌(MRSA)化合物。VP-4604对金黄色葡萄球菌展现出显著的抑制微生物生长的作用,MIC 为4-8μg/mL。VP-4604抑制耐甲氧西林金黄色葡萄球菌的生长,其生长抑制率达到95%以上。 | |||
T12126 |
MUT056399
Fab-001 |
Antibacterial | Microbiology/Virology |
MUT056399 (Fab-001) 是一种金黄色葡萄球菌和大肠杆菌的 FabI 酶的高效抑制剂,IC50值分别为 12 nM 和 58 nM。 | |||
TQ0063 |
Zoliflodacin
ETX0914,AZD0914 |
DNA gyrase; DNA/RNA Synthesis; Topoisomerase; Antibacterial | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Zoliflodacin (ETX0914) 是一种新型螺旋嘧啶三酮,对革兰氏阳性和阴性生物有抗菌活性,对金黄色葡萄球菌的b>MIC90值为0.25 μg/mL。他也是细菌DNA 促旋酶/拓扑异构酶的抑制剂。 | |||
T22387 |
NSC 55655
5-[(2-nitrophenyl)methylidene]thiazolidine-2,4-dione |
Others | Others |
NSC 55655 (5-[(2-Nitrophenyl)methylene]-2,4-thiazolidinedione) 具有抗菌和抗氧化活性,抑制 B. subtilis, S. aureus, K. pneumonia, E. coli, S. typhi ,A. niger 和 C. albicans 的增殖,可用于糖尿病。 | |||
T4208 |
Targocil
|
Antibacterial | Microbiology/Virology |
Targocil 是一种磷壁酸生物合成的抑菌抑制剂,可抑制甲氧西林敏感金黄色葡萄球菌 (MSSA) 和耐甲氧西林金黄色葡萄球菌 (MRSA) 的生长,对于 MRSA 和 MSSA 的MIC90值都为 2 μg/mL。 | |||
T20936 |
Lauramine oxide
LDAO,Dimethylaurylamine oxide,十二烷基二甲基氧化胺,Refan,Lauryldimethylamine oxide |
Antibacterial | Microbiology/Virology |
Lauramine oxide (Refan) 对大肠杆菌和金黄色葡萄球菌等常见细菌有效,但它是非变性的,可用于溶解蛋白质。 | |||
T61159 |
Antibacterial agent 26
|
Antibacterial | Microbiology/Virology |
Antibacterial agent 26 是一种抗菌化合物,是有效的DHFR 抑制剂(金黄色葡萄球菌DHFR Ki 为0.020 nM)。 | |||
T23725L |
Amicoumacin A FA
Amicoumacin A FA(78654-44-1 Free base) |
Antibacterial | Microbiology/Virology |
Amicoumacin A FA 具有抗菌活性,抑制紫罗兰色杆菌和金黄色葡萄球菌,可用与研究微生物感染。 | |||
TP1663L |
CysHHC10 acetate
CysHHC10 acetate(1408311-03-4 free base) |
Antibacterial | Microbiology/Virology |
CysHHC10 acetate 对革兰氏阳性菌和革兰氏阴性菌均具有抗菌活性,对大肠杆菌、铜绿假单胞菌、金黄色葡萄球菌和表皮葡萄球菌的 MIC 分别为 10.1、20.2、2.5 和 1.3 mM。 | |||
T6638 |
Retapamulin
瑞他莫林,SB-275833 |
ribosome; Antibacterial; Antibiotic | Microbiology/Virology |
Retapamulin (SB-275833) 是一种能结合金黄色葡萄球菌和大肠杆菌核糖体的局部抗生素,Kd 为3 nM。 | |||
T63390L |
(S,S)-TAPI-1 FA
(S,S)-TAPI-1 FA(171235-71-5 Free base) |
TNF | Apoptosis |
(S,S)-TAPI-1 FA是 TNF-α加工抑制剂,具有潜在抗炎作用,可阻断 TACE,可抑制 TNF-α 信号传导可用于研究金黄色葡萄球菌关节炎。 | |||
TQ0113 |
Iclaprim
艾拉普林,AR-100 |
Antibacterial; Antibiotic | Microbiology/Virology |
Iclaprim (AR-100) 是一种细菌二氢叶酸的选择性新型抑制剂, 可抑制金黄色葡萄球菌的生长, 其 MIC90值为 0.06 μg/mL。 | |||
T10586L |
BPH-1358
NSC50460 |
Others; Antibacterial | Microbiology/Virology; Others |
BPH-1358 (NSC-50460) 是一种人 FPPS 和 UPPS 抑制剂,IC50值分别为 1.8 μM 和 110 nM,对金黄色葡萄球菌的 MIC 值大约为 250 ng/mL。 | |||
T28229 |
Olanexidine hydrochloride
OPB2045,OPB-2045,OPB-2045 HCl,OPB 2045 |
Antibacterial | Microbiology/Virology |
Olanexidine hydrochloride (OPB-2045 HCl) 对革兰氏阳性菌和革兰氏阴性菌具有杀菌活性。 Olanexidine hydrochloride 破坏金黄色葡萄球菌的膜完整性。 | |||
TN6672 |
Cyclo(L-Phe-L-Pro)
|
Free radical scavengers; COX; Antibacterial; Antifungal | Immunology/Inflammation; Microbiology/Virology; Neuroscience; oxidation-reduction |
Cyclo(L-Phe-L-Pro) 具有广谱抗菌和抗真菌活性。 Cyclo(L-Phe-L-Pro) 对耐甲氧西林金黄色葡萄球菌和棉子肠球菌具有活性。 | |||
TP1412 |
RNAIII-inhibiting peptide TFA
RNAIII-inhibiting peptide(TFA),L-酪氨酰-L-丝氨酰-L-脯氨酰-L-色氨酰-L-苏氨酰-L-天冬氨酰胺酰-L-苯丙氨酸 |
Antibacterial | Microbiology/Virology |
RNAIII-inhibiting peptide TFA (RNAIII-inhibiting peptide(TFA))(228544-21-6 free base) 抑制肽(TFA)抑制金黄色葡萄球菌,对蜂窝织炎、角膜炎、化脓性关节炎、骨髓炎和乳腺炎等疾病有效。 | |||
T26755 |
BC-7013
BC7013,BC 7013 |
Antibacterial | Microbiology/Virology |
BC-7013 是一种新型胸膜植物素,具有抗菌活性,抑制革兰氏阳性病原菌 (bacteria) 活性,可用于研究皮肤和呼吸道感染。 | |||
T19642 |
Nilofabicin
CG 0549,CG-0549,CG-400549,CG 400549,CG0549,CG400549 |
Antibacterial | Microbiology/Virology |
Nilofabicin (CG-400549) 是一种有效的烯酰-(酰基-载体-蛋白)还原酶下降(FabI)抑制剂,可用于治疗复杂急性疾病的研究。 | |||
TP1773L |
PGLa acetate
|
Antibacterial; Antibiotic | Microbiology/Virology |
PGLa acetate 是 magainin 抗生素肽家族的 21 个残基成员。 | |||
T21358 |
Dalbavancin
BI 397,BI-397,VER 001,A-A 1,BI397,VER-001,Dalbavancin HCl,达巴万星 |
Antibacterial; Antibiotic | Microbiology/Virology |
Dalbavancin (BI-397) HCl 是一种半合成的脂糖肽抗生素,对革兰氏阳性细菌有杀菌活性。Dalbavancin 抑制金黄色葡萄球菌和炭疽芽孢杆菌的 MIC90分别为 0.06 μg/mL 和 0.25 μg/mL。 | |||
T2331 |
Solithromycin
索利霉素,OP-1068,CEM-101 |
Antibacterial; Antibiotic | Microbiology/Virology |
Solithromycin (OP-1068) 是口服可生物利用的抗菌剂,抑制肺炎链球菌、葡萄球菌、金黄色葡萄球菌和流感嗜血杆菌的细胞活力、蛋白质合成和生长速率, IC50 值分别为 7.5 ng/mL、40 ng/mL 和 125 ng/mL。它可与核糖体的大 50S 亚基结合抑制蛋白质生物合成。 | |||
T72330 |
Antibacterial agent 19
|
Others | Others |
Antibacterial agent 19 是一种有效的抗菌剂。Antibacterial agent 19 对K. pneumoniae,(M-R)S. aureus 和 (M-R,V-R)S. aureus 具有抗菌活性, 其 MIC 值为 0.022, 0.022 和 0.045 mg/mL。 | |||
T10587 |
BPH-652
|
Others | Others |
BPH-652 is an S. aureus dehydrosqualene synthase (CrtM) inhibitor (Ki: 1.5 nM; IC50: 100-300 nM for S. aureus pigment formation). | |||
T36594 |
4-Chloroguaiacol
|
Others | Others |
4-Chloroguaiaco (4-Chloro-2-methoxyphenol) is a phenol derivative, with antimicrobial activity. 4-Chloroguaiaco shows inhibition against S. aureus and E. coli with MICs of both 110 μg/mL[1]. [1]. Patrícia Fontes Pinheiro, et al. Semisynthetic Phenol Derivatives Obtained from Natural Phenols: Antimicrobial Activity and Molecular Properties. J Agric Food Chem. 2018 Jan 10;66(1):323-330. | |||
T76658 |
SYNV-cyclo(CGGYF)
|
||
SYNV-cyclo(CGGYF),一种源自人葡萄球菌(S. hominis)C5的自诱导肽,能抑制金黄色葡萄球菌(S. aureus)的活性,展现出研究金黄色葡萄球菌引发的上皮损伤及炎症的潜力。 | |||
T80293 |
RP-1
|
||
RP-1为一抗菌肽,具备针对S. aureus、S. typhimurium、E. coli及C. albicans的抗菌活性。 | |||
T76658L |
SYNV-cyclo(CGGYF) TFA
|
||
SYNV-cyclo(CGGYF) TFA 是人葡萄球菌 (S. hominis)C5 自诱导肽,能够抑制金黄色葡萄球菌 (S. aureus) 的活性,并具备探索金黄色葡萄球菌 (S. aureus) 引发的上皮损伤和炎症潜力。 | |||
T27389 |
Frequentin
|
Others | Others |
Frequentin, an antibiotic originally isolated from P. frequentans, is active against bacteria (MICs = 200 and 300 µg/ml for B. subtilis and S. aureus, respectively) and fungi. | |||
T70386 |
QZN34
|
Others | Others |
QZN34 is a PqsR inhibitor which prevents S. aureus biofilm formation, severely damaged established S. aureus biofilms, and perturbed P. aeruginosa biofilm development. The mechanism of action of QZN 34 toward Gram-positive bacteria is shown to involve membrane perturbation and dissipation of transmembrane potential. | |||
T38102 |
Decatromicin B
|
Others | Others |
Decatromicin B is a bacterial metabolite that has been found in Actinomadura. It is active against Gram-positive bacteria, including several strains of S. aureus (MICs = 0.39-0.78 μg/ml), two strains of methicillin-resistant S. aureus (MRSA; MICs = 0.39 and 0.78 μg/ml), as well as M. luteus, B. subtilis, and C. bovis (MICs = 0.78, 0.78, and 6.25 μg/ml, respectively). | |||
T36032 |
Desotamide
|
Others | Others |
Desotamide is a cyclic hexapeptide antibiotic originally isolated from Streptomyces. It is active against S. aureus, S. pneumoniae, and methicillin-resistant S. epidermidis (MRSE; MICs = 16, 12.5, and 32 μg/ml, respectively). | |||
T38334 |
Corynecin III
|
Others | Others |
Corynecin III is a chloramphenicol-like antibiotic originally isolated from Corynebacterium. It inhibits the growth of Gram-positive and Gram-negative bacteria, including S. faecalis, S. aureus, B. subtilis, E. coli, P. aeruginosa, P. vulgaris, S. sonnei, S. typhosa, and K. pneumoniae (MICs = 2.6-83 μg/ml). | |||
T64069 |
Antibacterial agent 87
|
Others | Others |
Antibacterial agent 87 是一种有效的抗细菌剂,能够作用于 MRSA (MIC: 0.125 μg/ml)、MRSE (MIC: 0.0625 μg/ml) 和 S. aureus (MIC: 0.0625 μg/ml)。 | |||
T38290 |
Leucomycin A4
Leucomycin A4 |
Others | Others |
Leucomycin A4 is a macrolide antibiotic that has been found in S. kitasatoensis. It is active against a variety of bacteria, including S. aureus, B. subtilis, C. diphtheriae, N. gonorrhoeae, and H. influenzae (MICs = 0.15, 1.25, 0.15, 0.6, and 0.15 μg/ml, respectively). | |||
T80047 |
Polistes mastoparan
|
||
Polistes mastoparan 作为一种抗菌肽,能够增强S. aureus (金黄色葡萄球菌) 的K+流失并削弱其活性,其EC50为5 μM。 | |||
T77111 | Omodenbamab | ||
Omodenbamab 是一种抗 SpA(葡萄球菌蛋白 A) 人源化单克隆抗体,KD 值为 0.0467 nM。Omodenbamab 通过靶向细胞壁部分蛋白 A (SpA) 来规避关键的 S. aureus 逃避机制。Omodenbamab 可用于 S. aureus 血流感染的研究。 | |||
T80414 |
ASP-1
|
||
ASP-1是一种活性强的抗葡萄球菌肽,其对金黄色葡萄球菌及耐甲氧西林金黄色葡萄球菌(MRSA)的最低抑制浓度(mic)范围为2μg/mL至64μg/mL。 | |||
T37465 |
CAY10742
|
Others | Others |
CAY10742 is an orally bioavailable oxadiazole antibiotic.1It is active against the Gram-positive bacteriaS. aureus,S. epidermidis,S. haemolyticus,B. cereus,B. licheniformis,E. faecalis, andE. faecium(MICs = 1-4 μg/ml), including laboratory strains and clinical isolates with varying degrees of resistance to methicillin, vancomycin, linezolid, and other antibiotics. CAY10742 (40 mg/kg) reduces the number of bacteria in mouse neutropenic thigh models of linezolid-sensitive or -resistant methicillin... | |||
T13149 |
Thiocillin I
|
Antibacterial | Microbiology/Virology |
Thiocillin I is a thiopeptide antibiotic and has in vitro antibacterial activity against Gram-positive bacterial strains(MIC of Thiocillin I against S. aureus 1974149, E. faecalis 1674621, B. subtilis ATCC 6633 and S. pyogenes 1744264 are 2 μg/mL, 0.5 μg/mL, 4 μg/mL and 0.5 μg/mL, respectively). |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5780 |
HYPOCRELLIN B
|
Apoptosis; Parasite; Antifungal | Apoptosis; Microbiology/Virology |
Hypocrellin B 是从真菌Hypocrella bambusae 和Shiraia bambusicola 中分离得到的一种感光颜料,可用于癌症光动力研究。它是一个凋亡诱导剂,还拥有抗菌和抗利什曼活性。 | |||
T3381 |
Lysionotin
岩豆素 |
Others | Others |
Lysionotin (Nevadensin) 是一种类黄酮,分离自黄花草药中。它可抑制 α-Toxin (一种成孔蛋白) 的表达,并在体内和体外针对金黄色葡萄球菌显示出显著的保护作用。它可用于研究由金黄色葡萄球菌引起的肺炎。 | |||
T5802 |
Stearyl glycyrrhetinate
|
Antiviral; Antibacterial | Immunology/Inflammation; Microbiology/Virology |
Stearyl glycyrrhetinate 是甘草提取物中的主要成分之一,具有抗菌作用,对金黄色葡萄球菌菌株的 MIC 大于 256 mg/L。 | |||
TN2730 |
2,5-Dihydroxybenzaldehyde
Gentisaldehyde,2,5-二羟基苯甲醛 |
Anti-infection; Antibacterial | Microbiology/Virology |
2,5-Dihydroxybenzaldehyde (Gentisaldehyde) 是一种天然抗微生物剂,可抑制Mycobacterium avium subsp. paratuberculosis 的生长。它还抑制金黄色葡萄球菌菌株,MIC50为 500 mg/L。 | |||
T1126 |
Penicillin V Potassium
青霉素V钾,Penicillin V potassium salt,Phenoxymethylpenicillin potassium salt |
Antibacterial; Antibiotic | Microbiology/Virology |
Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) 是一种有口服活性的抗生素。它可抑制链球菌,艰难梭菌和金黄色葡萄球菌的生长,可研究中耳炎,鼻窦炎,咽炎和扁桃体炎。 | |||
T8384 |
Gatifloxacin hydrochloride
AM-1155 (hydrochloride),BMS-206584 (hydrochloride),PD135432 (hydrochloride),加替沙星盐酸盐 |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Gatifloxacin hydrochloride (AM-1155 hydrochloride) 是一种氟喹诺酮类抗生素,有广谱抗菌活性。它可抑制大肠杆菌 DNA 解旋酶 (IC50=0.109 μg/ml)和细菌 II 型拓扑异构酶(IC50=13.8 μg/ml) 。它在动物模型中,可研究细菌性结膜炎。 | |||
T13708 |
Glycol chitosan
羟乙基脱乙酰壳多糖,乙二醇壳聚糖 |
Antibacterial | Microbiology/Virology |
Glycol chitosan 是具有亲水性乙二醇支链的壳聚糖衍生物。它抑制大肠杆菌,金黄色葡萄球菌和肠炎链球菌的生长,MIC 值分别为 4 μg/mL,32 μg/m L 和 <0.5 μg/mL。它可增强 Glycine max Harosoy 63W 细胞的膜通透性和渗漏。 | |||
TN1524 |
Continentalic acid
|
NOS; COX; Antibacterial; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Continentalic acid 是来自 Aralia continentalis 的,对金黄色葡萄球菌的 MIC 约为 8-16 µg/mL,包括对甲氧西林敏感的金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌标准菌株。 | |||
T37753 |
Aureusimine B
|
Cysteine Protease; Antibacterial | Microbiology/Virology; Proteases/Proteasome |
Aureusimine B 是一种钙蛋白酶抑制剂,由金黄色葡萄球菌生物膜产生,可能是金黄色葡萄球菌生物膜感染的潜在生物标志物。 | |||
TN7094 |
Coreoside B
|
Antibacterial | Microbiology/Virology |
Coreoside B 是从coreoside 中分离出来的,对金黄色葡萄球菌和炭疽杆菌显示出较弱的抗菌活性。 | |||
T37267 |
Pachybasin
|
Antibacterial | Microbiology/Virology |
Pachybasin 是一种蒽醌真菌代谢物。 Pachybasin 对大肠杆菌、枯草芽孢杆菌、M. luteus、S. cerevisiae、C. albicans、A. niger 和 A. flavus 具有抗菌活性,MIC 值为 64.0 μg/mL,对金黄色葡萄球菌具有抗菌活性 和尖孢镰刀菌,MIC 值分别为 32.0 和 16.0 μg/mL。 | |||
TN2281 |
Sinapaldehyde
trans-3,5-Dimethoxy-4-hydroxy cinnamaldehyde,TRANS-3,5-二甲氧基-4-羟基肉桂醛,芥子醛 |
Antibacterial | Microbiology/Virology |
Sinapaldehyde (trans-3,5-Dimethoxy-4-hydroxy cinnamaldehyde) 对耐甲氧西林的金黄色葡萄球菌和大肠杆菌有抗菌作用,MIC 值都为 128 μg/mL。 | |||
TN2898 |
Kaempferol-7,4'-dimethyl ether
3,5-Dihydroxy-4',7-dimethoxyflavone |
Antioxidant; Antifection | Microbiology/Virology; oxidation-reduction |
Kaempferol-7,4'-dimethyl ether 是从 Zingiber phillipseae 的根茎中分离得到的,对金黄色葡萄球菌和大肠杆菌具有抗氧化活性,MIC 分别为 200 和 225 μg/ml。 | |||
TN1949 |
Moracin C
桑辛素 C,5-(6-羟基-2-苯并呋喃基)-2-(3-甲基-2-丁烯基)-1,3-苯二醇 |
ROS; NO Synthase | Immunology/Inflammation |
Moracin C 是一种发现于Morus mesozygia、Morus alba var. multicaulis 中的天然化合物,是一种抗炎剂。Moracin C 可抑制细胞中的一氧化氮(NO)释放和LPS 激活的活性氧(ROS)。 | |||
TN2447 |
Isovalerylshikonin
|
Antibacterial | Microbiology/Virology |
Isovalerylshikonin 是太子参和紫草的天然产物。 | |||
T6S0525 |
Farrerol
|
ERK; p38 MAPK; Akt | Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling |
Farrerol 是一种杜鹃花的生物活性成分,具有抗氧化、抗肿瘤、抗炎、神经保护和肝保护等多种功能。 | |||
T13305 |
Viridicatol
|
Anti-infection; Antifungal | Microbiology/Virology |
Viridicatol 是从夹竹桃的内生真菌青霉菌属的发酵中分离出的一种喹诺酮类生物碱,对金黄色葡萄球菌有抗菌活性,MIC 值为 15.6 μg/mL。 | |||
T5S1981 |
alpha-Cyperone
(+)-α-Cyperone,α-香附酮,α-Cyperone |
Others; Endogenous Metabolite | Metabolism; Others |
alpha-Cyperone (α-Cyperone) 与 IL-6, Cox-2, Cdc42, Nck-2, Rac1 的表达下调相关,从而能够抑制炎症反应。 | |||
TN1722 |
Hamamelitannin
|
Antifection | Microbiology/Virology |
Hamamelitannin 是分离自 Hamamelis virginiana 树皮的一种多酚,是群体感应抑制剂。它通过影响肽聚糖生物合成和 eDNA 释放增加金黄色葡萄球菌生物膜的抗生素敏感性。 | |||
TN3861 |
Dihydropinosylvin
山药 |
Anti-infection | Microbiology/Virology |
Dihydropinosylvin 是一种植物抗毒素,对枝孢枝孢菌、Botryodiplodia theobromae、黑曲霉和石化青霉具有抗真菌活性,对蜡状芽孢杆菌、金黄色葡萄球菌、铜绿假单胞菌和大肠杆菌也有很强的抗菌活性。双色高粱幼苗的种子和根伸长。 | |||
T6873 |
Lauric Acid
月桂酸,Dodecylic acid,dodecanoic acid,Vulvic acid,N-Dodecanoic acid |
Others; Endogenous Metabolite; Antibacterial | Metabolism; Microbiology/Virology; Others |
Lauric Acid (Dodecylic acid) 是一种有抗菌活性的中链脂肪酸,对P. acnes,S.aureus 和S. epidermidis 的 EC50值分别为 2,6,4 μg/mL。 | |||
TC0017 |
Haplopine
|
Tyrosinase; Antifection | Microbiology/Virology; Proteases/Proteasome |
Haplopine shows photo-activated antimicrobial activity against S. aureus. It exhibits potent melanogenesis-inhibitory activities with almost no toxicity to the cells. | |||
TN3216 |
(3R)-7,4’-Dihydrohomoisoflavanone
7,4'-Dihydroxyhomoisoflavanone |
Antibacterial | Microbiology/Virology |
(3R)-7,4’-Dihydrohomoisoflavanone 是一种天然化合物,对金黄色葡萄球菌和耐甲氧西林金黄色葡萄菌(MRSA)都具有强大的抗菌性能。 | |||
T72805 |
(±)-Hydnocarpin
|
Others | Others |
(±)-Hydnocarpin 是一种黄酮木脂素。(±)-Hydnocarpin 可以抑制S. aureus 的生长,MIC50值为 3.1 μM。 | |||
T27024 |
Citromycetin
Frequentic Acid,NSC-53584,NSC 53584,NSC53584 |
Others | Others |
Citromycetin is a fungal metabolite originally isolated from Australian P. frequentans. It has antibiotic activity against the Gram-negative bacteria V. cholerae and S. flexneri and the Gram-positive bacteria S. aureus. | |||
TN4725 |
Oxychelerythrine
|
Antifection | Microbiology/Virology |
Oxychelerythrine shows high modulatory activity enhancing the susceptibility of the S. aureus ATCC 6538 to all the tested antibiotics from two to four-fold. It also shows antifeeding activities against Tribolium castaneum adults, with the EC50 of 192.32 p | |||
TN2809 |
22-Dehydroclerosterol
|
Antifection | Microbiology/Virology |
22-Dehydroclerosterol has antibacterial activity against against E. coli, S. aureus, and H. pylori. | |||
TN7563 |
Chloramphenicol Acetate
|
Others | Others |
Chloramphenicol acetate, an acetylated and inactive derivative of chloramphenicol, is synthesized in E. coli and S. aureus through the action of the inducible enzyme chloramphenicol acetyltransferase, utilizing acetyl coenzyme A (acetyl-CoA), to impart resistance to chloramphenicol. This compound exhibits no antibiotic activity against S. sonnei in turbidimetric assays. | |||
T35754 |
Aszonapyrone A
|
Others | Others |
Aszonapyrone A is a meroditerpene fungal metabolite that has been found in Neosartorya and has diverse biological activities.1,2,3 It inhibits the growth of MCF-7, NCI H460, and A375-C5 cancer cells (GI50s = 13.6, 11.6, and 10.2 μM, respectively).1 Aszonapyrone A is active against multidrug-resistant isolates of S. aureus, E. faecalis, and E. faecium (MICs = 8, 16, and 16 μg/ml, respectively) and inhibits S. aureus biofilm formation.2 It is also active against P. falciparum in vitro (IC50 = 1.34... | |||
T36417 |
Nargenicin
Antibiotic 47444 |
Others | Others |
Nargenicin is a macrolide antibiotic that selectively inhibits the growth of S. aureus, methicilin resistant S. aureus (MRSA), and M. luteus (MICs = 0.6, 0.3, and 2.5 μg/ml, respectively) over a panel of 11 Gram-positive and Gram-negative bacteria (MICs = >80 μg/ml). [1] It dose-dependently inhibits S. aureus DnaE in the presence of DNase I-activated DNA and E. coli DnaE when used at concentrations of 0.00001-0.1 and 0.01-100 μg/mL, respectively. [2] In murine BV-2 microglial cells, nargenicin (... | |||
TN1526 |
Corydalmine
|
P450; Antifection | Metabolism; Microbiology/Virology |
Corydalmine exhibits antibacterial activities against Staphylococcus aureus and methicillin-resistant S. aureus strains.1-Corydalmine significantly inhibits spore germination of all the fungi at 100 to 1500 ppm. l-Corydalmine also exhibits potent analgesic activity in preclinical models, it is under development as an oral analgesic agent. | |||
TN7525 |
Parvodicin C2
Antibiotic A40926 B1 |
Others | Others |
Parvodicin C2, a glycopeptide antibiotic derived from A. parvosata and part of the parvodicin complex, serves as a component of the A40926 antibiotic complex utilized as a precursor for synthesizing dalbavancin. It exhibits activity against methicillin-sensitive and methicillin-resistant strains of S. aureus, S. epidermidis, S. saprophyticus, S. hemolyticus, and E. faecalis. | |||
TN3573 |
Camaric acid
|
Antifection | Microbiology/Virology |
Camaric acid shows antibacterial activity against Staphylococcus aureus and methicillin resistant S. aureus with IC50 values 8.74 and 8.09 uM, respectively, it also shows moderate antileishmanial activity and highly potent antitrypanosomal activity. Camar | |||
TN5404 |
(+)-Conocarpan
|
||
Conocarpan has antinociceptive effects. Conocarpan is quite active against S. aureus and B. subtilis with MIC of 6.25 micrograms/ml, it also shows activity against M. tuberculosis (MIC=15.6 ug/ml). Conocarpan shows considerable activity against epimastigo | |||
TN6010 |
Picrasidine S
|
||
Picrasidine S shows the potent cytotoxicity against human HeLa cervical, gastric MKN-28, and mouse melanoma B-16 cancer cells, it also shows the potent antibacterial activity against two strains of pathogenic bacteria methicillin-resistant Staphylococcus | |||
TN3978 |
Epitaraxerol
|
Antifection | Microbiology/Virology |
Epitaraxerol shows moderate antifungal activity against C. albicans and low antimicrobial activity against T. mentagrophytes, A. niger, S. aureus, E. coli, P. aeruginosa, and B. subtilis. | |||
T69058 |
OM173-αA
|
Others | Others |
OM173-αA is a quinone bacterial metabolite that inhibits the growth of the bacteria M. gallisepticum, M. pneumoniae, and S. aureus. OM173-αA also inhibits the growth of the plant pathogenic fungus P. oryzae and several species of Trichophyton. | |||
T36044 |
17-hydroxy Venturicidin A
|
Others | Others |
17-hydroxy Venturicidin A is a macrolide fungal metabolite originally isolated from Streptomyces. It has antibiotic activity against M. luteus, B. subtilis, and S. aureus and antifungal activity against V. dahlia, Fusarium, and C. tropicalis in a disc assay. | |||
T83862 |
Bactobolin A hydrochloride
BN-183B |
Others | Others |
Bactobolin A 是一种最初从 Pseudomonas 中分离出的微生物代谢产物,具有抗生素和抗癌活性。它对 S. aureus、S. epidermidis、S. faecalis、B. anthracis、B. subtilis、E. coli、S. typhi 和 S. dysenteriae 活跃(MICs = 0.1-12.5 µg/ml)。在体内,bactobolin A (0.25-4 mg/kg) 提高了 L1210 小鼠白血病模型的存活率。 | |||
TN3404 |
Altholactone
|
BCL; p38 MAPK; ROS; Akt; Caspase; Antifection; p53 | Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; MAPK; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Altholactone may be a potential antimicrobial agent, particularly in ciprofloxacin-refractory S. aureus and E. faecalis infections. It can inhibit the growth of various types of cancer cells through inducing apoptosis via oxidative stress, including bladd | |||
T37442 |
Aspergillin PZ
|
Others | Others |
Aspergillin PZ is a fungal metabolite originally isolated from A. awamori. It induces morphological deformation of P. oryzae conidia when used at a concentration of 89 nM. Aspergillin PZ is active against S. epidermidis (MIC = 20 μM) but not S. aureus, E. coli, or B. cereus (MICs = >20 μM). It is cytotoxic to HL-60 promyelocytic leukemia cells (IC50 = 56.61 μM) but not THP-1 acute monocytic leukemia or PC3 prostate cancer cells (IC50s = >80 μM). | |||
TN4319 |
Isopimaric acid
|
Antifection | Microbiology/Virology |
Isopimaric acid is active against MDR and MRSA strains of S. aureus which are becoming increasingly resistant to antibiotics, the minimum inhibitory concentrations (MIC) are 32-64 microg/mL . Isopimaric acid is also possible that an antagonistic interacti | |||
T72235 |
Antibacterial synergist 2
|
Others | Others |
Antibacterial synergist 2 是菌膜抑制剂。Antibacterial synergist 2 对肠球菌、金色葡萄球菌、铜绿假单胞菌和白色假单胞菌具有抑制效应。Antibacterial synergist 2 可用于与形成菌膜的病原体的相关研究。 | |||
TN4264 |
Isoapetalic acid
胡桐,海棠木 |
HIV Protease; Antifection | Microbiology/Virology; Proteases/Proteasome |
Isoapetalic acid and apetalic acid exhibit cytotoxic activities towards both cancer cell lines(human breast cancer (MCF-7) and human lung carcinoma (A-549) cell lines) and both Gram-positive bacteria(two Gram-positive bacteria, S. aureus and B. subtilis a | |||
TN5466 |
Boeravinone B
|
||
Boeravinone B, a novel efflux pump inhibitor, apart from inhibiting the MdeA mediated efflux, also significantly inhibit the biofilm formation of S. aureus, boeravinone B may be used in combination with mupirocin for further development. Boeravinone B exh | |||
T83918 |
Clazamycin A hydrochloride
NSC 332188 |
Others | Others |
Clazamycin A是一种最初从链霉菌中分离出的抗生素和微生物代谢产物。它对多种细菌具有活性,包括S. aureus、B. anthracis、B. subtilis、E. coli和P. aeruginosa(MICs分别为100、6.25、100、50和25 µg/ml)。 | |||
T38086 |
Neohydroxyaspergillic Acid
|
Others | Others |
Neohydroxyaspergillic acid is a fungal metabolite produced by A. sclerotiorum that has antibiotic and antifungal activities. It inhibits the growth of P. aeruginosa, M. smegmatis, S. aureus, E. coli, K. pneumoniae, B. mycoides, and B. subtilis bacteria (MICs = 125-500 μg/ml). Neohydroxyaspergillic acid also inhibits the growth of G. convolute, S. consortiale, P. blakesleeanus, C. globosum, and T. mentagrophytes (MICs = 175-700 μg/ml) but not A. niger, P. notatum, M. verrucaria, or S. cerevisiae ... | |||
T38097 |
Antibiotic PF 1052
|
Others | Others |
Antibiotic PF 1052 is a fungal metabolite originally isolated from Phoma.1,2 It is active against S. aureus, S. parvulus, and C. perfringens (MICs = 3.13, 0.78, and 0.39 μg/ml, respectively), among others.1 It inhibits neutrophil migration in a wound assay using zebrafish larvae expressing GFP-labeled neutrophils, reducing pseudopodia formation and inducing rounding of neutrophils.2 Antibiotic PF 1052 is selective for neutrophil migration over macrophage migration in zebrafish larvae. It also in... | |||
T38016 |
Hirsutide
|
Others | Others |
Hirsutide is a cyclotetrapeptide fungal metabolite produced by the entomopathogenic fungus Hirsutella. It has antibacterial activity against C. pyogenes, S. aureus, P. aeruginosa, and K. pneumonia (MICs = 25, 13, 6, and 21 μg/cm3, respectively). Hirsutide also has antifungal activity against C. albicans, M. audouinii, A. niger, and Ganoderma (MICs = 13, 6, 25, and 6 μg/cm3, respectively). | |||
T80330 |
XT-1
|
Others | Others |
XT-1是一种抗菌肽,源自热带爪蟾Xenopus tropicalis的皮肤分泌物,表现出对S.aureus、E.coli和C.albicans的强烈活性,其最小抑菌浓度(MIC)分别为5μM、6μM和50μM。 | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-03575 |
Sortase A Protein, S. aureus, Recombinant (His)
Surface protein sorting A,srtA, |
Staphylococcus aureus | E. coli |
Sortase A Protein, S. aureus, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 24.9 kDa and the accession number is Q2FV99. | |||
TMPH-03557 |
HlgC Protein, S. aureus, Recombinant (His)
hlgC,Gamma-hemolysin component C |
Staphylococcus aureus | P. pastoris (Yeast) |
Toxin that seems to act by forming pores in the membrane of the cell. Has a hemolytic and a leucotoxic activity. HlgC Protein, S. aureus, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 34.6 kDa and the accession number is Q7A3S2. | |||
TMPH-03555 |
HlgB Protein, S. aureus, Recombinant (His)
H-gamma-I,hlgB,Gamma-hemolysin component B,H-gamma-... |
Staphylococcus aureus | P. pastoris (Yeast) |
Toxin that seems to act by forming pores in the membrane of the cell. Has a hemolytic and a leucotoxic activity. HlgB Protein, S. aureus, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 36.1 kDa and the accession number is P0A075. | |||
TMPH-03518 |
ACP Protein, S. aureus, Recombinant (GST)
acpP,Fatty acid synthase acyl carrier prot... |
Staphylococcus aureus | E. coli |
Carrier of the growing fatty acid chain in fatty acid biosynthesis. Is able to confer high methicillin resistance to S.aureus when overproduced. ACP Protein, S. aureus, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 35.5 kDa and the accession number is P0A001. | |||
TMPH-03563 |
MCAT Protein, S. aureus, Recombinant (His)
fabD,Malonyl CoA-acyl carrier protein transacyla |
Staphylococcus aureus | P. pastoris (Yeast) |
MCAT Protein, S. aureus, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 35.6 kDa and the accession number is Q5HGK3. | |||
TMPH-03519 |
ACP Protein, S. aureus, Recombinant (His)
Cytosolic-activating factor,Fatty acid syn... |
Staphylococcus aureus | P. pastoris (Yeast) |
Carrier of the growing fatty acid chain in fatty acid biosynthesis. Is able to confer high methicillin resistance to S.aureus when overproduced. ACP Protein, S. aureus, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 10.5 kDa and the accession number is P0A001. | |||
TMPH-03527 |
FtsZ Protein, S. aureus, Recombinant (His)
ftsZ,Cell division protein FtsZ |
Staphylococcus aureus | E. coli |
Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity. FtsZ Protein, S. aureus, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The ... | |||
TMPH-03558 |
LytM Protein, S. aureus, Recombinant (His)
Autolysin LytM,Glycyl-glycine endopeptidas... |
Staphylococcus aureus | E. coli |
Peptidoglycan hydrolase (autolysin) specifically acting on polyglycine interpeptide bridges of the cell wall peptidoglycan. LytM Protein, S. aureus, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 35.9 kDa and the accession number is O33599. | |||
TMPH-03574 |
SdrE Protein, S. aureus, Recombinant (His)
sdrE,Serine-aspartate repeat-cont... |
Staphylococcus aureus | E. coli |
Cell surface-associated calcium-binding protein which plays an important role in adhesion and pathogenesis. Contributes to the resistance to killing by innate immune components in blood and thus attenuates bacterial clearance by interacting with host complement factor H/CFAH and modulating its activity. Inhibits also bacterial opsonization and killing by interacting with host complement regulator C4BPA and thus inhibiting classical complement pathway activation. SdrE Protein, S. aureus, Recombin... | |||
TMPH-03572 |
SplB Protein, S. aureus, Recombinant (His & Myc)
splB,Serine protease Spl... |
Staphylococcus aureus | E. coli |
Serine protease that cleaves specifically after the sequence Trp-Glu-Leu-Gln. SplB Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 29.8 kDa and the accession number is A7X3Q8. | |||
TMPH-03516 |
NPTase Protein, S. aureus, Recombinant (His & SUMO)
30 kDa neutral phosphatase |
Staphylococcus aureus | E. coli |
Highly cationic enzyme that can bind human or rat immunoglobulins as well as serum albumin, and could therefore be involved in post-infectious sequelae. NPTase Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 19.7 kDa and the accession number is P21222. | |||
TMPH-03566 |
Peptide deformylase Protein, S. aureus, Recombinant (His)
Polypeptide deformylase,def,Peptide deformylas<... |
Staphylococcus aureus | P. pastoris (Yeast) |
Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. Peptide deformylase Protein, S. aureus, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 22.6 kDa and the accession number is P68826. | |||
TMPH-03568 |
Phospholipase C Protein, S. aureus, Recombinant (His)
hlb,Beta-hemolysin,Phospholipase ... |
Staphylococcus aureus | P. pastoris (Yeast) |
Bacterial hemolysins are exotoxins that attack blood cell membranes and cause cell rupture. Beta-hemolysin is a phospholipase C with specific activity toward sphingomyelins. Has a high specificity for sphingomyelin, hydrolyzes lysophosphatidylcholine at a much lower rate, but has no activity towards phosphatidylcholine, phosphatidylethanolamine, or phosphatidylserine. Phospholipase C Protein, S. aureus, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 3... | |||
TMPH-03550 |
EsxA Protein, S. aureus, Recombinant (His & SUMO)
esxA,Type VII secretion sys |
Staphylococcus aureus | E. coli |
Virulence factor that is important for the establishment of infection in the host. EsxA is required for EsxB synthesis as well as secretion. Modulates host cell apoptotic pathways and mediates together with EsxB the release of S.aureus from the host cell. By acting on apoptosis, plays a role in the modulation of dendritic cell-mediated immunity. EsxA Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 27.... | |||
TMPH-03578 |
SCIN Protein, S. aureus, Recombinant (His & Myc)
scn,Staphylococcal complement inhibitor |
Staphylococcus aureus | E. coli |
Involved in countering the first line of host defense mechanisms. Efficiently inhibits opsonization, phagocytosis and killing of S.aureus by human neutrophils. Acts by binding and stabilizing human C3 convertases (C4b2a and C3bBb), leading to their inactivation. The convertases are no longer able to cleave complement C3, therefore preventing further C3b deposition on the bacterial surface and phagocytosis of the bacterium. Also prevents C5a-induced neutrophil responses. SCIN Protein, S. aureus, ... | |||
TMPH-03564 |
MCAT Protein, S. aureus, Recombinant (His & SUMO)
Malonyl CoA-acyl carrier protein transacylas |
Staphylococcus aureus | E. coli |
MCAT Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 49.6 kDa and the accession number is Q5HGK3. | |||
TMPH-03553 |
HlgA Protein, S. aureus, Recombinant (His & Myc)
H-gamma-II,H-gamma-2,Gamma-hemolysin component A,hl... |
Staphylococcus aureus | E. coli |
Toxin that seems to act by forming pores in the membrane of the cell. Has a hemolytic and a leucotoxic activity. HlgA Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 39.4 kDa and the accession number is P0A073. | |||
TMPH-03565 |
MazF Protein, S. aureus, Recombinant (His)
Toxin MazF,mRNA interferase MazF,mazF,Endoribonucle... |
Staphylococcus aureus | E. coli |
Toxic component of a type II toxin-antitoxin (TA) system. Ribosome-independent, sequence-specific endoribonuclease that cleaves mRNA, thus inhibiting protein synthesis and inducing bacterial stasis. It cuts between the first and nucleotides of 5'-UACAU-3' in single-stranded RNA. Neutralized by coexpression with cognate antitoxin MazE. MazF Protein, S. aureus, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 17.4 kDa and the accession... | |||
TMPH-03577 |
Staphopain B Protein, S. aureus, Recombinant (GST)
Staphopain B,sspB,Staphy... |
Staphylococcus aureus | E. coli |
Cysteine protease that plays an important role in the inhibition of host innate immune response. Degrades host elastin, fibrogen, fibronectin and kininogen. Blocks phagocytosis of opsonised S. aureus by neutrophils and monocytes by inducing their death in a proteolytic activity-dependent manner. Decreases surface expression of the 'don't eat me' signal CD31 on neutrophils. Cleaves host galectin-3/LGALS3, thereby inhibiting the neutrophil-activating ability of the lectin. Staphopain B Protein, S.... | |||
TMPH-03571 |
WalK Protein, S. aureus, Recombinant (His & Myc)
walK,Sensor protein kinase WalK |
Staphylococcus aureus | E. coli |
WalK Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 29.3 kDa and the accession number is A6QD58. | |||
TMPH-03570 |
IsaA Protein, S. aureus, Recombinant (His & Myc)
Probable transglycosylase Is<... |
Staphylococcus aureus | E. coli |
Is able to cleave peptidoglycan. IsaA Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 28.8 kDa and the accession number is P60157. | |||
TMPH-03521 |
MecA Protein, S. aureus, Recombinant (His & SUMO)
Adapter protein MecA,mecA |
Staphylococcus aureus | E. coli |
Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis. MecA Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 44.3 kDa and the accession number is P60186. | |||
TMPH-03561 |
lsdB Protein, S. aureus, Recombinant (His & SUMO)
Fur-regulated protein B,Iron-regulated surface dete... |
Staphylococcus aureus | E. coli |
Cell wall-anchored surface receptor that extracts heme from oxidized metHb to enable growth on hemoglobin as a sole iron source. Rapidly extracts heme from hemoglobin and transfers it to IsdA or IsdC, which then relays it to the membrane transporter/IsdEF for internalization. Promotes also resistance to hydrogen peroxide and killing by neutrophils. lsdB Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is ... | |||
TMPH-03525 |
Cap5A Protein, S. aureus, Recombinant (His)
Capsular polysaccharide type 5 bios |
Staphylococcus aureus | E. coli |
Required for the biosynthesis of type 5 capsular polysaccharide (Cap5/CP5). Might act as the chain-length regulator. Cap5A Protein, S. aureus, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 26.4 kDa and the accession number is P95695. | |||
TMPH-03526 |
Cap8A Protein, S. aureus, Recombinant (His)
MAGEB2,MAGE XP-2 antigen,DAM6,MAGE-B2 antigen,Melanoma-a... |
Staphylococcus aureus | E. coli |
May enhance ubiquitin ligase activity of RING-type zinc finger-containing E3 ubiquitin-protein ligases. Proposed to act through recruitment and/or stabilization of the Ubl-conjugating enzyme (E2) at the E3:substrate complex. Cap8A Protein, S. aureus, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 26.4 kDa and the accession number is O15479. | |||
TMPH-03537 |
Enterotoxin type A Protein, S. aureus, Recombinant (His)
Enterotoxin type A,SEA,entA |
Staphylococcus aureus | E. coli |
Enterotoxin type A Protein, S. aureus, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 31.1 kDa and the accession number is P0A0L2. | |||
TMPH-03576 |
Staphopain A Protein, S. aureus, Recombinant (His & Myc)
Staphopain A,Staphylopain A,s... |
Staphylococcus aureus | E. coli |
Staphopain A Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 27.4 kDa and the accession number is P81297. | |||
TMPH-03540 |
Enterotoxin type B Protein, S. aureus, Recombinant (GST)
entB,Enterotoxin type B,SEB |
Staphylococcus aureus | E. coli |
Staphylococcal enterotoxin that activates the host immune system by binding as unprocessed molecules to major histocompatibility (MHC) complex class II and T-cell receptor (TCR) molecules. In turn, this ternary complex activates a large number of T-lymphocytes initiating a systemic release of proinflammatory cytokines. Causes also the intoxication staphylococcal food poisoning syndrome. Enterotoxin type B Protein, S. aureus, Recombinant (GST) is expressed in E. coli expression system with N-GST ... | |||
TMPH-03573 |
SplD Protein, S. aureus, Recombinant (His & Myc)
Serine protease SplD,spl... |
Staphylococcus aureus | E. coli |
SplD Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 29.5 kDa and the accession number is Q2FXC5. | |||
TMPH-03560 |
lsdA Protein, S. aureus, Recombinant (His & Myc)
Iron-regulated surface determinant protein A,S<... |
Staphylococcus aureus | E. coli |
lsdA Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 35.1 kDa and the accession number is Q6GA85. | |||
TMPH-03533 |
Ddl Protein, S. aureus, Recombinant (His & Myc)
ddl,D-alanylalanine synthetase,D-Ala-D-Ala... |
Staphylococcus aureus | E. coli |
Cell wall formation. Ddl Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 47.7 kDa and the accession number is P63891. | |||
TMPH-03520 |
ACP Protein, S. aureus, Recombinant (His & SUMO)
acpP,Cytosolic-activating factor,Fatty acid s |
Staphylococcus aureus | E. coli |
Carrier of the growing fatty acid chain in fatty acid biosynthesis. Is able to confer high methicillin resistance to S.aureus when overproduced. ACP Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 24.5 kDa and the accession number is P0A001. | |||
TMPH-03536 |
FabI Protein, S. aureus, Recombinant (His & SUMO)
Enoyl-[acyl-carrier-protein] reductase [NADPH] FabI... |
Staphylococcus aureus | E. coli |
Catalyzes the reduction of a carbon-carbon double bond in an enoyl moiety that is covalently linked to an acyl carrier protein (ACP). Involved in the elongation cycle of fatty acid which are used in the lipid metabolism. FabI Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 44.0 kDa and the accession number is Q6GI75. | |||
TMPH-03569 |
IcaB Protein, S. aureus, Recombinant (His & Myc)
Intercellular adhesion protein B,Poly-beta-1,6-N-ac... |
Staphylococcus aureus | E. coli |
Catalyzes the N-deacetylation of poly-beta-1,6-N-acetyl-D-glucosamine (PNAG, also referred to as PIA), a biofilm adhesin polysaccharide. N-deacetylation is crucial for attachment of the polysaccharide to the bacterial cell surface; it leads to the introduction of positive charges in the otherwise neutral PIA polymer, allowing electrostatic interactions. IcaB Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular ... | |||
TMPH-03522 |
Alpha-hemolysin Protein, S. aureus, Recombinant (His)
Alpha-toxin,Alpha-HL |
Staphylococcus aureus | P. pastoris (Yeast) |
Alpha-toxin binds to the membrane of eukaryotic cells resulting in the release of low-molecular weight molecules and leading to an eventual osmotic lysis. Inhibits host neutrophil chemotaxis to the lesion region (Probable). Heptamer oligomerization and pore formation is required for lytic activity. | |||
TMPH-03524 |
KAS III Protein, S. aureus, Recombinant (His & Myc)
3-oxoacyl-[acyl-carrier-protein] synthase ... |
Staphylococcus aureus | E. coli |
Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched-chain and/or straight-chain of fatty acids. KAS III Protein, S. au... | |||
TMPH-03551 |
Exfoliative toxin A Protein, S. aureus, Recombinant (His)
eta,Epidermolytic toxin A,Exfoliative toxin A |
Staphylococcus aureus | E. coli |
Has serine protease-like properties and binds to the skin protein profilaggrin. Cleaves substrates after acidic residues. Exfoliative toxins cause impetigous diseases commonly referred as staphylococcal scalded skin syndrome (SSSS). | |||
TMPH-03539 |
Enterotoxin type B Protein, S. aureus, Recombinant (His)
Enterotoxin type B,SEB,entB |
Staphylococcus aureus | P. pastoris (Yeast) |
Staphylococcal enterotoxin that activates the host immune system by binding as unprocessed molecules to major histocompatibility (MHC) complex class II and T-cell receptor (TCR) molecules. In turn, this ternary complex activates a large number of T-lymphocytes initiating a systemic release of proinflammatory cytokines. Causes also the intoxication staphylococcal food poisoning syndrome. | |||
TMPH-03538 |
Enterotoxin type A Protein, S. aureus, Recombinant (His & Myc)
Enterotoxin type A,SEA,entA |
Staphylococcus aureus | Baculovirus Insect Cells |
Enterotoxin type A Protein, S. aureus, Recombinant (His & Myc) is expressed in Baculovirus insect cells with N-10xHis and C-Myc tag. The predicted molecular weight is 31.0 kDa and the accession number is P0A0L2. | |||
TMPH-03545 |
Enterotoxin type E Protein, S. aureus, Recombinant (His & SUMO)
Enterotoxin type E,SEE,entE |
Staphylococcus aureus | E. coli |
Staphylococcal enterotoxin that activates the host immune system by binding as unprocessed molecules to major histocompatibility (MHC) complex class II and T-cell receptor (TCR) molecules. In turn, this ternary complex activates a large number of T-lymphocytes initiating a systemic release of proinflammatory cytokines. Causes also the intoxication staphylococcal food poisoning syndrome. | |||
TMPH-03559 |
Sbi Protein, S. aureus, Recombinant (Avi & His & MBP), Biotinylated
sbi,Immunoglobulin-binding protein Sbi |
Staphylococcus aureus | E. coli |
Plays a role in the inhibition of both the innate and adaptive immune responses. Possesses two N-terminal domains that bind the Fc region of IgG and two domains that form a tripartite complex with complement factors C3b and CFH. By recruiting CFH and C3b, the secreted form acts as a potent complement inhibitor of the alternative pathway-mediated lysis. Sbi Protein, S. aureus, Recombinant (Avi & His & MBP), Biotinylated is expressed in E. coli expression system with N-MBP and C-6xHis-Avi tag. The... | |||
TMPH-03556 |
HlgC Protein, S. aureus, Recombinant (E. coli, His)
hlgC,Gamma-hemolysin component C |
Staphylococcus aureus | E. coli |
Toxin that seems to act by forming pores in the membrane of the cell. Has a hemolytic and a leucotoxic activity. HlgC Protein, S. aureus, Recombinant (E. coli, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 36.6 kDa and the accession number is Q7A3S2. | |||
TMPH-03579 |
TSST-1 Protein, S. aureus, Recombinant (His & SUMO)
Toxic shock syndrome toxin-1,tst |
Staphylococcus aureus | E. coli |
Responsible for the symptoms of toxic shock syndrome. TSST-1 Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 37.9 kDa and the accession number is P06886. | |||
TMPH-03549 |
Enterotoxin type H Protein, S. aureus, Recombinant (His)
Enterotoxin type H,SEH,entH |
Staphylococcus aureus | P. pastoris (Yeast) |
Enterotoxin type H Protein, S. aureus, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 27.1 kDa and the accession number is P0A0M0. | |||
TMPH-03523 |
Alpha-hemolysin Protein, S. aureus, Recombinant (His & SUMO)
Alpha-HL,Alpha-toxin |
Staphylococcus aureus | E. coli |
Alpha-toxin binds to the membrane of eukaryotic cells resulting in the release of low-molecular weight molecules and leading to an eventual osmotic lysis. Inhibits host neutrophil chemotaxis to the lesion region (Probable). Heptamer oligomerization and pore formation is required for lytic activity. | |||
TMPH-03554 |
HlgB Protein, S. aureus, Recombinant (E. coli, His)
H-gamma-1,Gamma-hemolysin component B,H-gamma-I,hlg... |
Staphylococcus aureus | E. coli |
Toxin that seems to act by forming pores in the membrane of the cell. Has a hemolytic and a leucotoxic activity. HlgB Protein, S. aureus, Recombinant (E. coli, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 38.1 kDa and the accession number is P0A075. | |||
TMPH-03535 |
Dihydrofolate reductase Protein, S. aureus, Recombinant (His & Myc)
DHFR,Dihydrofolate reductase,folA |
Staphylococcus aureus | E. coli |
Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis. Dihydrofolate reductase Protein, S. aureus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 25.6 kDa and the accession number is P99079. | |||
TMPH-03531 |
ClfA Protein, S. aureus (strain COL), Recombinant (His)
Fibrinogen-binding protein A,clfA,Clumping factor A,Fibrinog... |
Staphylococcus aureus | P. pastoris (Yeast) |
Cell surface-associated protein implicated in virulence. Promotes bacterial attachment exclusively to the gamma-chain of human fibrinogen. Induces formation of bacterial clumps. ClfA Protein, S. aureus (strain COL), Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 38.0 kDa and the accession number is Q5HHM8. | |||
TMPH-03542 |
Enterotoxin type C-2 Protein, S. aureus, Recombinant
Enterotoxin type C-2,entC2,SEC2 |
Staphylococcus aureus | E. coli |
Staphylococcal enterotoxin that activates the host immune system by binding as unprocessed molecules to major histocompatibility (MHC) complex class II and T-cell receptor (TCR) molecules. In turn, this ternary complex activates a large number of T-lymphocytes initiating a systemic release of proinflammatory cytokines. Causes also the intoxication staphylococcal food poisoning syndrome. Enterotoxin type C-2 Protein, S. aureus, Recombinant is expressed in E. coli expression system. The predicted ... | |||
TMPH-03567 |
Peptide deformylase Protein, S. aureus, Recombinant (His & SUMO)
Peptide deformylase,def,Polypeptide deformylas<... |
Staphylococcus aureus | E. coli |
Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. Peptide deformylase Protein, S. aureus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 36.6 kDa and the accession number is P68826. | |||
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Cat. No. | Product Name | Target | Signaling Pathways |
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T69995 |
Chlorhexidine-d8 HCl
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Chlorhexidine-d8 is intended for use as an internal standard for the quantification of chlorhexidine by GC- or LC-MS. Chlorhexidine is a bis(biguanide) antimicrobial disinfectant and antiseptic agent. It inhibits growth of clinical methicillin-resistant S. aureus (MRSA) isolates (MIC90 = 4 μg/ml). It is also active against canine isolates of MRSA, methicillin-susceptible S. aureus (MSSA), methicillin-resistant S. pseudintermedius (MRSP), and methicillin-susceptible S. pseudintermedius (MSSP; MIC... | |||
T37250 |
Cefazolin-13C2,15N
Cefazolin-13C2,15N |
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Cefazolin-13C2,15N is intended for use as an internal standard for the quantification of cefazolin by GC- or LC-MS. Cefazolin is a broad-spectrum cephalosporin antibiotic that is active in vitro against various Gram-positive and Gram-negative bacteria (MICs = 0.2-12.5 μg/ml). It also inhibits the growth of clinical isolates of S. aureus, E. coli, P. mirabilis, and K. pneumoniae (MICs = 0.1-25 μg/ml). In vivo, cefazolin protects against S. aureus, E. coli, and P. mirabilis infection in mice (ED50... | |||
T36021 |
Flumequine-13C3
Flumequine-13C3 |
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Flumequine-13C3is intended for use as an internal standard for the quantification of flumequine by GC- or LC-MS. Flumequine is a fluoroquinolone antibiotic.1It is active againstS. aureus, S. pyogenes, B. subtilis, E. coli, P. aeruginosa, S. faecalis, andK. pneumoniae(MICs = 1-100 μg/ml). Flumequine is also active against field isolates of B. hyodysenteriae (MICs = 6.25-200 μg/ml).2It inhibits DNA gyrase, disrupting supercoiling of bacterial DNA to block transcription and replication.3In vivo, fl... |