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Cat. No. | Product Name | ||
---|---|---|---|
L9820 | β-内酰胺类化合物库 | 97 compounds | |
97 种β-内酰胺类化合物的集合,可以用于高通量和高内涵筛选; | |||
DO2200 | 共价抑制剂库CD | 12000 compounds | |
数量多:超过12000种共价结合化合物,并且数量在持续增加; | |||
L6500 | 微生物天然产物库 | 685 compounds | |
685 种微生物来源的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T60050 |
ANT3310
|
Antibacterial | Microbiology/Virology |
ANT3310 是一种广谱共价丝氨酸 β-内酰胺酶抑制剂,对 AmpC、CTX-M-15、TEM-1、OXA-48、OXA-23 和 KPC-2 的 IC50 范围为 1 nM 至 175 nM。 ANT3310 可用于细菌感染研究。 | |||
T14979 |
Clavulanate lithium
Clavulanic acid lithium,克拉维酸锂 |
Antibacterial | Microbiology/Virology |
Clavulanate lithium (Clavulanic acid lithium) 是一种β-lactamase 的高效抑制剂,可作抗生素。 | |||
T4405 |
Ceftibuten dihydrate
头孢布烯二水合物,Sch-39720 dihydrate |
Antibacterial; Antibiotic | Microbiology/Virology |
Ceftibuten dihydrate (Sch-39720 dihydrate) 是一种具有口服活性的头孢菌素,在体外对多种革兰氏阴性和某些革兰氏阳性病原体有抗菌活性。 | |||
T0234 |
Methicillin sodium salt
Methicillin sodium,Meticillin sodium,甲氧西林钠 |
Antibacterial; Antibiotic | Microbiology/Virology |
Methicillin sodium salt 是β-内酰胺抗生素,抑制参与肽聚糖合成的青霉素结合蛋白。 | |||
T6438 |
Cefoselis Sulfate
FK 037 Sulfate,FK-037,硫酸头孢噻利 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefoselis Sulfate (FK 037 Sulfate) 是一种头孢菌素 β-内酰胺抗生素。它对多种革兰氏阳性和革兰氏阴性生物均表现出良好的活性。它可以透过血脑屏障。 | |||
T37704 |
Olanzapine Lactam Impurity
|
Others | Others |
Olanzapine lactam impurity is a potential impurity found in commercial preparations of olanzapine.1It is a degradation product formed by exposure to thermal or oxidative stress. 1.Baertschi, S.W., Brunner, H., Bunnell, C.A., et al.Isolation, identification, and synthesis of two oxidative degradation products of olanzapine (LY170053) in solid oral formulationsJ. Pharm. Sci.97(2)883-892(2008) | |||
T36053 |
D-Lysine lactam
|
Others | Others |
D-Lysine lactam is a chiral building block.1,2It has been used in the synthesis of a chiral antibiotic synthetic intermediate, as well as in the stereoselective synthesis of neurokinin (NK) receptor antagonists. 1.Kumar, A., Bhashkar, B., Bhavsar, J., et al.Catalytic reduction: Efficient synthesis of chiral key intermediate of besifloxacin hydrochlorideDer Pharma Chemica7(9)297-3000(2015) 2.Gerspacher, M., Lewis, C., Ball, H.A., et al.Stereoselective preparation of N-[(R,R)-(E)-1-(3,4-dichlorobe... | |||
T36422 |
L-Lysine lactam (hydrochloride)
|
Others | Others |
L-lysine lactam is a building block.1,2It has been used in the synthesis of lysine sulfonamide HIV protease inhibitors, as well as bengamide derivatives within vitroanticancer activity. | |||
T68462 |
D-Ornithine lactam
|
Others | Others |
D-Ornithine lactam is a building block. It has been used in the synthesis of hepatitis C virus non-structural protein 5B inhibitors, as well as αVβ3 integrin receptor antagonists. | |||
T71831 |
L-Ornithine lactam hydrochloride
|
Others | Others |
L-Ornithine lactam is a synthetic intermediate. It has been used in the synthesis of dipeptidyl peptidase 4 (DPP-4) inhibitors, as well as signaling peptides. | |||
T6471 |
Dicloxacillin Sodium
Veracillin,双氯西林,BRL1702 Sodium,BRL1702,Sodium dicloxacillin,双氯西林钠 |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Dicloxacillin Sodium (BRL1702 Sodium) 是一种青霉素类窄谱β内酰胺抗生素, 用于革兰氏阳性菌感染的研究。它对β-内酰胺酶产生的微生物有抗菌作用。 | |||
T0827 |
Cefsulodin sodium
Cefsulodine sodium,Sulcephalosporin,头孢磺啶钠 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefsulodin sodium (Sulcephalosporin) 是β内酰胺抗生素,对缘脓杆菌和肠杆菌有活性。 | |||
T5570 |
Cephalothin
头孢噻吩,Cephalotin acid |
Antibacterial; Antibiotic | Microbiology/Virology |
Cephalothin 是一种 β-内酰胺抗生素,抑制 C 类 β-内酰胺酶活性的 Ki 值为 0.32 µM。 | |||
T6385 |
Amoxicillin Sodium
阿莫西林钠,Clavulanate |
Antibacterial; Antibiotic | Microbiology/Virology |
Amoxicillin Sodium (Clavulanate) 是一种有广谱抗菌活性,口服吸收好的抗生素。它能抑制细胞壁中多肽的生物合成,可抑制细胞生长。 | |||
T1001 |
Dicloxacillin Sodium hydrate
Dicloxacillin sodium salt monohydrate,双氯西林钠,Dicloxacillin sodium monohydrate |
Antibacterial; Antibiotic | Microbiology/Virology |
Dicloxacillin Sodium hydrate 是一种青霉素类窄谱β内酰胺抗生素,可研究革兰氏阳性菌感染。 | |||
T74149 |
JPD447
|
Antibacterial | Microbiology/Virology |
JPD447是MAC-0547630衍生物,可增强β-内酰胺类抗生素的 UppS 抑制剂,具有抗菌活性,可用于研究细菌感染。 | |||
T12166 |
Nacubactam
OP0595 free acid,那库巴坦 |
Antibacterial | Microbiology/Virology |
Nacubactam (OP0595 free acid) 是一种非 β-内酰胺-β-内酰胺酶抑制剂,对 A 类和 C 类 β-内酰胺酶具有活性。它作为青霉素结合蛋白 2 活性抗菌剂,并赋予 β-内酰胺酶非依赖性增强作用以靶向其他 PBP。 | |||
T1305 |
Ceftazidime
GR20263,头孢他啶 |
Antibacterial; Antibiotic | Microbiology/Virology |
Ceftazidime (GR20263) 是可静脉内或肌肉给药的第头孢菌素。它对革兰氏阳性和革兰氏阴性需氧细菌有体外活性。它对肠杆菌科特别有效,对大多数 β-内酰胺酶具有抗水解作用。 | |||
T6582 |
Mezlocillin Sodium
美洛西林钠,Baycipen |
Antibacterial; Antibiotic | Microbiology/Virology |
Mezlocillin Sodium (Baycipen) 是一种青霉素 β-内酰胺类抗生素,用于治疗由易感染微生物引起的细菌感染。 | |||
T11265 |
Faropenem daloxate
法罗培南酯,Faropenem medoxil |
Antibacterial; Antibiotic | Microbiology/Virology |
Faropenem daloxate (Faropenem medoxil) 是β-内酰胺类口服抗生素。 | |||
T28165 |
NF-1819
NF 1819,NF1819 |
Lipase | Metabolism |
NF-1819 是一种高效、选择性的不可逆 MGL (β-内酰胺基单酰甘油脂肪酶)抑制剂。NF-1819 在体内多发性硬化症模型中缓解疾病症状,在体内急性炎性疼痛模型中表现出镇痛作用。NF-1819 具有较高的膜通透性和血脑屏障通透性。 | |||
T1631 |
Sulbactam
CP45899,舒巴坦,舒巴坦酸 |
Antibacterial; Antibiotic | Microbiology/Virology |
Sulbactam (CP45899) 是一种竞争性、不可逆的 β-内酰胺酶抑制剂,抑制耐多药不动杆菌-鲍曼不动杆菌复合物。它具有抗菌活性。 | |||
T19860 |
Clavulanic Acid
BRL 14151,MM-14151,MM 14151,RX-10100,MM14151,BRL14151,BRL-14151 |
Antibacterial; Antifungal | Microbiology/Virology |
Clavulanic Acid(RX-10100) 是一种由生物体克拉维链霉菌产生的主要β-内酰胺类抗生素,是一种强效的细菌 β-内酰胺酶抑制剂,用于研究细菌引起的感染。Clavulanic Acid 具有广谱的生物活性,对多种革兰氏阳性和革兰氏阴性细菌均有活性。 | |||
T28880 |
Sulfazecin free acid
G 6302,Antibiotic G 6302,Sulfazecin,Antibiotic EM 5210 |
Others | Others |
Sulfazecin is a β-Lactam antibiotic. | |||
T1070L |
Cefmetazole
Sodium, Cefmetazole,Cefmetazolum,Cefmetazolo |
Others | Others |
Cefmetazole is a second-generation semi-synthetic β-lactam cephalosporin antibiotic with antimicrobial activity. | |||
T11341 |
FXIa-IN-1
|
Others | Others |
FXIa-IN-1 is a potent β-lactam covalent heparin-derived factor XIa (fXIa) inhibitor. | |||
T30510 |
BMS-262084
BMS 262084,I0IR71971G,UNII-I0IR71971G,CHEMBL71037 |
Others | Others |
BMS-262084 is a potent selective β-lactam trypsin inhibitor with therapeutic potential in the treatment of asthma. | |||
T0814L1 |
L-(+)-Ampicillin
Ampicillin,L-Ampicillin |
Others | Others |
L-(+)-Ampicillin is an isomer of Ampicillin. Ampicillin is a β-lactam antibiotic used for treating bacterial infections. | |||
T24010 |
DNAC-1
DNAC 1,DNAC1 |
Others | Others |
DNAC-1 is against Gram-positive and Gram-negative pathogens potentiator of β-lactam activity. | |||
T26465 |
A1-226
A1226 |
Others | Others |
A1-226 is a cephalosporin of the class of β-lactam antibiotics, it is originally derived from the fungus Acremonium. | |||
T16466 |
Penicillin G Procaine
PGP |
Others | Others |
Penicillin G Procaine is a β-lactam antibiotic and is a crystalline complex produced by chemically combining penicillin G with procaine. | |||
T26980 |
Cephamycin C
A 16886B,A16886B, A-16886B |
Others | Others |
Cephamycin C (CepC) is a nontoxic β-lactam antibiotic. CepC stands out from other cephalosporins for its greater resistance to β-lactamases. | |||
T36600 |
Cefsulodin (sodium salt hydrate)
|
Others | Others |
Cefsulodin is a β-lactam antibiotic that lyses actively-growingE. coliby binding specifically to the intermembrane proteins, penicillin-binding proteins 1a and b, whose transglycosylase and transpeptidase activities are involved in cell elongation and septation.1Cefsulodin has been used in combination with other β-lactam antibiotics, such as cefazolin as a strategy to circumvent drug resistance.2 | |||
T39811 |
D-4-Hydroxyphenylglycine
4-Hydroxy-D-phenylglycine,D-(-)-4-Hydroxyphenylglycine,D-4-Hydroxyphenylglycine |
Others | Others |
D-4-Hydroxyphenylglycine (D-(-)-4-Hydroxyphenylglycine) is a crucial raw material in the synthesis of semisynthetic β-lactam antibiotics, including Amoxicillin and Cefadroxil . | |||
T75391 |
Penicillinase
|
Others | Others |
Penicillinase 是一种 β-内酰胺酶。β-内酰胺酶通过水解特征性四元 β-内酰胺环的肽键使抗生素失效,从而使 β-内酰胺抗生素失活。 | |||
T10422 |
Avibactam free acid
NXL-104 free acid |
Antibacterial | Microbiology/Virology |
Avibactam (NXL-104) free acid is a covalent and reversible inhibitor of non-β-lactam β-lactamase (IC50s: 8 nM and 5 nM for β-lactamase TEM-1 and CTX-M-15). | |||
T21384 |
Dicloxacillin
Dicloxacilina,Dicloxacycline,Dicloxacillinum,Dicloxacilline,Diclocil,Dynapen |
Others | Others |
Dicloxacillin (INN), a narrow-spectrum β-Lactam antibiotic of the penicillin class, is used against beta-lactamase-producing organisms such as Staphylococcus aureus, which would otherwise be resistant to most penicillins. | |||
T40203 |
AZD-CO-Ph-PEG4-Ph-CO-AZD
AZD-CO-Ph-PEG4-Ph-CO-AZD |
Others | Others |
AZD-CO-Ph-PEG4-Ph-CO-AZD is a bis-β-lactam linker, commonly employed in the synthesis of antibody-siRNA conjugates. | |||
T38972 |
Cefalonium hydrate
|
Others | Others |
Cefalonium hydrate is a first-generation β-lactam cephalosporin antibiotic commonly employed in the study of bovine mastitis induced by Gram-positive bacteria, particularly staphylococci. It demonstrates significant effectiveness in this research area. | |||
T70774 |
Clavicoronic acid
|
Others | Others |
Clavicoronic acid is a β-lactam drug that functions as a mechanism-based β-lactamase inhibitor. While not effective by itself as an antibiotic, when combined with penicillin-group antibiotics, it can overcome antibiotic resistance in bacteria that secrete β-lactamase, which otherwise inactivates most penicillins. | |||
T38020 |
O-Benzylhydroxylamine (hydrochloride)
|
Others | Others |
O-Benzylhydroxylamine is a building block.1,2It has been used in the synthesis of β-lactam inhibitor precursors and fluoroquinolone derivatives with antibiotic activity. 1.Bellettini, J.R., and Miller, M.J.A short synthesis of an important precursor to a new class of bicyclic β-lactamase inhibitorsTetrahedron Lett.38(2)167-168(1997) 2.Asadipour, A., Moshafi, M.H., Khosravani, L., et al.N-substituted piperazinyl sarafloxacin derivatives: synthesis and in vitro antibacterial evaluationDaru.26(2)19... | |||
T68149 |
tacapenem
|
Others | Others |
Tacapenem 是一种β-内酰胺类抗菌剂。它具有广谱抗菌活性,对β-内酰胺酶具有很高的稳定性。 | |||
T34270 |
Razupenem
SMP601,SMP 601,PTZ601,PTZ 601,PTZ-601,SMP-601 |
Others | Others |
Razupenem ( SMP-601, PTZ601) is a broad-spectrum injectable antibiotic derived from the carbapenem subgroup of β-lactam antibiotics. It has been developed as an alternative drug against bacteria that have developed antibiotic resistance to commonly used a | |||
T32064 |
Hetacillin
Hetacilina,Hetacilline,Hetacillinum,Phenazacillin,Versapen |
Others | Others |
Hetacillin 是一种β-内酰胺抗生素,属于氨基青霉素家族,通过酯酶转化为氨苄西林。氨苄西林是一种没有抗菌活性的前药。 | |||
T73600 |
Cefaloglycin
|
Others | Others |
Cefaloglycin(Cephaloglycin)是一种β-内酰胺类(β-lactam)口服活性头孢菌素类抗生素,具有肾毒性和抗菌活性。该药物对革兰氏阳性球菌(除肠球菌外)有效,同时对线粒体底物摄取及呼吸具有毒性。 | |||
T60874 |
Avibactam sodium dihydrate
|
Others | Others |
Avibactam sodium (NXL-104) dihydrate 抑制 CTX-M-15和 β-内酰胺酶 TEM-1,IC50值分别为 5 nM 和 8 nM。Avibactam sodium (NXL-104) dihydrate 是非 β-内酰胺 β-内酰胺酶的可逆共价抑制剂。 | |||
T60711 |
Avibactam sodium hydrate
|
Others | Others |
Avibactam sodium hydrate (NXL-104 hydrate) 是 β-内酰胺酶的共价可逆抑制剂,不含β-内酰胺核心 。Avibactam sodium hydrate 抑制 β-内酰胺酶CTX-M-15和TEM-1,IC50分别为5 nM 和 8 nM。 | |||
T74917 |
KPC-2-IN-1
|
Others | Others |
KPC-2-IN-1,硼酸衍生物,是一种有效的 KPC-2抑制剂,其 Ki 值为 0.032 μM。KPC-2-IN-1 能增强 cefotaxime 在表达 KPC-2的大肠杆菌中的活性。KPC-2-IN-1 对人类 HEK-293 细胞显示良好的耐受性,可用于大肠杆菌耐β-lactam 类抗生素的研究。 | |||
T68866 |
Ceftolozane
|
Others | Others |
Ceftolozane, also known as FR-264,205 and CXA-101; is an antibiotic drug from the cephalosporin family, approved for the treatment of infections with gram-negative bacteria, or gram-positive bacteria. Ceftolozane is of great benefit due to its ability to target bacteria that have become resistant to conventional antibiotics. Ceftolozane is combined with the β-lactamase inhibitor tazobactam, as multi-drug resistant bacterial infections will generally show resistance to all β-lactam antibiotics un... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8261 |
Ceftazidime Pentahydrate
头孢他啶五水合物,头孢他啶 |
Antibacterial; Antibiotic | Microbiology/Virology |
Ceftazidime pentahydrate 是一种β-内酰胺类抗菌剂,对革兰氏阳性和革兰氏阴性需氧细菌有广谱活性,可静脉内或肌肉给药。它对肠杆菌科特别有效,对大多数 β-内酰胺酶具有抗水解作用。 | |||
T0814 |
Ampicillin Trihydrate
NCI-C56086,氨苄青霉素三水合物 |
Antibacterial; Antibiotic | Microbiology/Virology |
Ampicillin Trihydrate (NCI-C56086) 是一种 β-内酰胺类广谱抗生素,可对抗多种革兰氏阳性和革兰氏阴性细菌。 | |||
T1029 |
Aztreonam
SQ-26,776,氨曲南 |
Antibacterial; Antibiotic | Microbiology/Virology |
Aztreonam (SQ-26,776) 是单环β-内酰胺抗生素,与青霉素结合蛋白3有较高亲和力。 | |||
T0814L |
Ampicillin
Amcill,D-(-)-α-Aminobenzylpenicillin,Aminobenzylpenicillin,氨苄青霉素,Ampicillin acid |
Antibacterial; Antibiotic | Microbiology/Virology |
Ampicillin (Aminobenzylpenicillin) 属于 β-内酰胺类抗生素,是一种半合成的青霉素。Ampicillin 具有杀菌活性,对各种革兰氏阳性细菌和革兰氏阴性细菌均有抑制活性。 | |||
T1505 |
Imipenem monohydrate
N-Formimidoyl thienamycin monohydrate,亚胺培南,Imipenem,亚胺培南一水物 |
Antibacterial; Antibiotic | Microbiology/Virology |
Imipenem monohydrate (Imipenem) 是从微生物 Streptomyces cattleya 分离得到的碳青霉烯类抗生素,是一种用于静脉注射的β 内酰胺类抗生素,作用于细菌细胞壁,能广泛有效抑制多种革兰氏阳性和阴性菌。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMID-0004 |
Ampicillin-d5
|
||
Ampicillin-d5 是 Ampicillin 的氘代化合物。Ampicillin 的 CAS 号为 69-53-4。Ampicillin是一种广谱、半合成的β-内酰胺类青霉素抗生素,具有杀菌活性。 | |||
TMIH-0530 |
Sulbactam-d2
|
||
Sulbactam-d2 是 Sulbactam 的氘代化合物。Sulbactam 的 CAS 号为 68373-14-8。Sulbactam是一种竞争性、不可逆的 β-内酰胺酶抑制剂,抑制耐多药不动杆菌-鲍曼不动杆菌复合物。它具有抗菌活性。 |