58
6
5
8
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8365 |
Methenamine Hippurate
|
Antibacterial | Microbiology/Virology |
Methenamine hippurate 是一种口服活性尿液广谱抗菌剂。它对大多数常见的尿路病原体有效。 | |||
T8133 |
SulfadiMethoxine sodium
|
Anti-infection; Antibacterial; Antibiotic | Microbiology/Virology |
SulfadiMethoxine sodium 是一种磺胺类抗生素,可研究由多种感染引起的疾病。 | |||
T1070 |
Cefmetazole sodium
头孢美唑钠,Sodium cefmetazole |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefmetazole sodium (Sodium cefmetazole) 是具有广谱抗菌活性的半合成头孢霉素抗生素。它通过与青霉素结合蛋白结合,阻止肽聚糖的交联,导致细胞壁完整性的丧失。它可研究妇科、腹腔内、尿道、呼吸道和皮肤和软组织感染。 | |||
T1444 |
Lomefloxacin
洛美沙星,SC47111A |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Lomefloxacin (SC47111A) 是一种广谱喹诺酮类抗生素,具有抗菌活性。它可研究支气管炎、尿路感染、结膜炎、外耳炎和中耳炎。 | |||
T1078 |
Sulfadimethoxine
Sulphadimethoxine,磺胺二甲氧嗪 |
Antibacterial; Antibiotic | Microbiology/Virology |
Sulfadimethoxine (Sulphadimethoxine) 是一种磺胺类抗生素,用于多种感染引起的疾病的研究。 | |||
T16789 |
Rosoxacin
罗索沙星,Acrosoxacin |
Antibacterial; Antibiotic | Microbiology/Virology |
Rosoxacin (Acrosoxacin) 是具有口服活性的喹诺酮类抗生素,具有广谱的抗菌活性,抑制革兰氏阴性菌,包括淋病奈瑟氏球菌(MIC90=0.03 mg/ml)。它在尿路感染中有应用的潜能。 | |||
T5521 |
Bropirimine
U-54461,溴匹立明 |
TLR | Immunology/Inflammation |
Bropirimine (U-54461) 是 toll 样受体 7(TLR7)的合成激动剂,可通过 TLR7 介导 IFN-β 的产生抑制破骨细胞前体细胞向破骨细胞分化。它是一种生物反应调节剂,通过诱导淋巴因子起作用,在膀胱和上尿路的原位移行细胞癌中具有抗癌活性。 | |||
T0116 |
Balofloxacin
|
DNA gyrase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Balofloxacin 是一种具有口服活性的氟喹诺酮类抗生素,可通过干扰 DNA 促旋酶来抑制细菌 DNA 的合成,对革兰氏阴性,革兰氏阳性和厌氧菌具有广谱抗菌活性。它可研究呼吸道,肠道和泌尿道感染。 | |||
T5513 |
RO-3
|
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
RO3 是一种能透过大脑的P2X3和P2X2/3拮抗剂,口服有活性。它对人同型多聚体 P2X3和异型多聚体 P2X2/3受体的 pIC50分别为 5.9 和 7.0。 | |||
T6349 |
Sitafloxacin Hydrate
西他沙星水合物,DU-6859a,DU6859a hydrate |
Antibacterial; Antibiotic | Microbiology/Virology |
Sitafloxacin Hydrate (DU-6859a) 是一种口服有效的氟喹诺酮类抗生素,在体外可对抗广泛的革兰氏阳性和阴性细菌有活性。Sitafloxacin 可研究呼吸道感染和尿路感染。 | |||
T0274 |
Cinoxacin
西诺沙星,Compound 64716 |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Cinoxacin (Compound 64716) 是一种喹诺酮类的合成抗生素, 与Oxolinic acid 和 Nalidixic acid 活性相似。 | |||
T0748 |
Sulfameter
5-Methoxysulfadiazine,Sulfametoxydiazine,磺胺对甲氧嘧啶 |
DHFR; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Sulfameter (Sulfametoxydiazine) 是一种长效磺胺类抗生素,具有抗菌活性。它可研究尿路感染和麻风病。 | |||
T1625 |
Lomefloxacin hydrochloride
Lomefloxacin HCl,盐酸洛美沙星,Okacyn,Maxaquin |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Lomefloxacin hydrochloride (Okacyn) 是一种广谱喹诺酮类抗生素,具有抗菌活性。它可研究支气管炎、尿路感染、结膜炎、外耳炎和中耳炎。 | |||
T8139 |
Sulfamethoxazole sodium
新诺明钠,Ro 4-2130 sodium,磺胺甲恶唑钠 |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Sulfamethoxazole sodium (Ro 4-2130 sodium) 是一种磺胺类抗菌素。它常用于各种尿道病原体的研究,与 Trimethoprim 联用,可用于尿路感染的研究。 | |||
T1504 |
Silodosin
西洛多辛,KAD 3213,KMD 3213 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Silodosin (KAD 3213) 是有选择性的、强效的、口服活性的 α1A-adrenergic receptor 阻滞剂,是一种有效且耐受性良好的试剂,可用于研究 LUTS/BPH。它对 α1A-AR 表现出高度的亲和力,是 α1B-AR 和 α1D-AR 亲和力的 162 和 50 倍。 | |||
T1233 |
Oxolinic acid
Emyrenil,Nidantin,NSC 110364,恶喹酸,Dioxacin,Urinox |
Dopamine Receptor; DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; GPCR/G Protein; Microbiology/Virology; Neuroscience |
Oxolinic acid (Nidantin) 是一种抗生素,对革兰氏阴性菌和革兰氏阳性菌均有效,可研究急性和慢性尿路感染。它是一种 DNA/RNA 合成抑制剂,也是一种多巴胺摄取抑制剂,能刺激小鼠的活跃过度。 | |||
T5189 |
Omadacycline
PTK 0796,Amadacycline |
ribosome; Antibacterial; Antibiotic | Microbiology/Virology |
Omadacycline (Amadacycline) 是一种具有口服活性的氨基甲基环素抗菌剂,是四环素类抗生素。它与 30S 核糖体亚基结合,抑制细菌蛋白质合成。它可用于研究急性细菌性皮肤和皮肤结构感染,感染性肺炎和尿路感染。 | |||
T0703 |
Flavoxate hydrochloride
Flavoxate HCl,盐酸黄酮哌酯,NSC-114649,DW61,Rec-7-0040 |
AChR | Neuroscience |
Flavoxate hydrochloride (DW61) 是一种毒蕈碱受体 AChR 拮抗剂, IC50为 12.2 μM。 | |||
T6349L |
Sitafloxacin
DU-6859A,Sitafloxacin anhydrous,DU 6859,DU6859,DU-6859,DU 6859A,DU6859A |
Antibiotic | Microbiology/Virology |
Sitafloxacin (Sitafloxacin anhydrous) 是一种具有口服活性的氟喹诺酮类抗生素,具有广谱的抗菌活性。Sitafloxacin 可用于研究呼吸道感染和尿路感染。 | |||
T4273 |
Furagin
F-35,Akritoin,Furazidine,NF-416,呋喃烯啶,Furazidin |
Antibacterial | Microbiology/Virology |
Furagin (Furazidine) 是 nitrofurantoin 类似物,有抗菌活性,用于尿路感染。 | |||
T0400 |
Nitroxoline
5-Nitro-8-quinolinol,8-Hydroxy-5-nitroquinoline,5-Nitro-8-hydroxyquinoline,5-nitroquinolin-8-ol,硝羟喹啉 |
Antibacterial; Antibiotic; Autophagy | Autophagy; Microbiology/Virology |
Nitroxoline (5-nitroquinolin-8-ol) 是一种抗生素,防治生物膜感染。它通过从生物膜基质螯合Fe2+和Zn2+离子而发挥作用。 | |||
T22316 |
Doxazosin
UK 33274,多沙唑嗪 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Doxazosin (UK 33274) 是选择性的拮抗突触后的α1肾上腺素受体。 | |||
T2184 |
Sulfachloropyridazine
Sulfachlorpyridazine,磺胺二甲基嘧啶 |
Antibacterial; Antibiotic | Microbiology/Virology |
Sulfachloropyridazine (Sulfachlorpyridazine) 是一种广谱磺酰胺,抑制革兰氏阳性和革兰氏阴性好氧细菌的生长。 | |||
T0026 |
Sulfalene
磺胺林,Sulfalene(SMPZ),Sulfalen,SMP2,Butadiene sulfone,AS-18908,Sulfametopyrazine,3-Sulfolene |
Antibacterial; Antibiotic; Parasite; Autophagy | Autophagy; Microbiology/Virology |
Sulfalene (SMP2) 是一种长效磺胺类抗生素,用于治疗慢性支气管炎、尿路感染和疟疾。 | |||
T9420 |
prifinium bromide
|
Others | Others |
Prifinium bromide 是抗胆碱能试剂,能够改善痉挛,具有止吐效果。 | |||
T0087L |
Sulfacetamide sodium
Sulamyd sodium,磺乙酰胺钠盐,磺胺醋酰钠 |
Antibacterial; Antibiotic; Autophagy | Autophagy; Microbiology/Virology |
Sulfacetamide sodium (Sulamyd sodium) 是磺胺类抗感染剂,可局部用于口服治疗尿路感染和皮肤感染。 | |||
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。 | |||
T0170 |
Phosphonic acid, [(2R,3S)-3-methyloxiranyl]-, calcium salt (9CI)
phosphonomycin calcium,Fosfomycin calcium,磷霉素钙,phosphomycin calcium |
Antibiotic | Microbiology/Virology |
Phosphonic acid, [(2R,3S)-3-methyloxiranyl]-, calcium salt (9CI) (phosphonomycin calcium)是一种抗生素,用于治疗敏感菌株引起的尿路感染和肠道感染。 | |||
T35851 |
Etzadroxil
Ethyl 2-Ethylbutyrate |
Antibacterial | Microbiology/Virology |
Etzadroxil (Ethyl 2-Ethylbutyrate) 是一种可口服且具有挥发性的酯化物。Etzadroxil 具有广谱的抗菌活性,可用于治疗由多重耐药细菌引起的尿路感染。 | |||
T8134 |
Cefathiamidine
|
Antibacterial; Antibiotic | Microbiology/Virology |
Cefathiamidine 是一种头孢菌素抗菌剂,可研究由易感细菌引起的感染,还可用于呼吸道、肝脏、五官感觉、尿路感染以及心内膜炎和败血症的研究。 | |||
T21369 |
Mecillinam
Amdinocillin,Mecillinamum,Hexacillin,美西林,Coactin,Penicillin HX |
Antibacterial | Microbiology/Virology |
Mecillinam (Hexacillin) 是一种有抗革兰氏阴性菌活性的 β 内酰胺类广谱抗生素。 | |||
T9422 |
Fosciclopirox
CPX-POM |
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
Fosciclopirox (CPX-POM) 利用靶向γ-分泌酶,抑制尿路上皮癌的生长。静脉给药后,它选择性地将活性代谢物 Ciclopirox 递送至整个尿路。Ciclopirox 在许多实体和血液恶性肿瘤中显示出抗癌活性。 | |||
T8722 |
iKIX1
|
Antifungal | Microbiology/Virology |
iKIX1 是一种 Pdr1 依赖性基因激活。 它在体外和在播散性和泌尿道光滑念珠菌感染的动物模型中使耐药的光滑念珠菌对唑类抗真菌剂重新敏感。它可研究多药耐药性和光滑念珠菌感染。 | |||
T9449 |
Nitrofural
[(E)-(5-nitrofuran-2-yl)methylideneamino,(E)-2-((5-硝基呋喃-2-基)亚甲基)肼甲酰胺 |
Antibacterial | Microbiology/Virology |
Nitrofural 是 20 世纪已在临床应用中确立的硝基呋喃。 Nitrofural 在临床上对广泛的革兰氏阳性和革兰氏阴性细菌(包括许多常见的泌尿道病原体菌株)仍然有效。 | |||
T3126 |
Bethanechol chloride
(±)-Bethanechol,Urecholine,Myocholine,氯贝胆碱,Carbamyl-β-methylcholine chloride |
AChR | Neuroscience |
Bethanechol chloride (Carbamyl-β-methylcholine chloride) 是一种拟副交感神经剂,是毒蕈碱型受体 (mAChR) 激动剂,通过直接刺激副交感神经系统的 mAChR 发挥作用。 | |||
T1386 |
Phenazopyridine hydrochloride
Urodine,Pyridium,Phenazopyridine HCl,盐酸非那吡啶 |
Sodium Channel | Membrane transporter/Ion channel |
Phenazopyridine hydrochloride (Pyridium) 是一种具有局部止痛作用的化学物质,常被用于缓解手术、损伤尿道及尿路感染引起的疼痛、刺激、不适和尿急。 | |||
T22232 |
Alfuzosin
SL 77499 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Alfuzosin (SL 77499) 是一种可口服且具有竞争性的 α1-肾上腺素受体拮抗剂。Alfuzosin 诱导膀胱颈和前列腺的平滑肌松弛。Alfuzosin 可用于研究良性前列腺肥大、下尿路症状 (LUTS)和射精功能障碍 (EjD)。 | |||
T26974 |
Cefetamet Hydrochloride
Cefetamet HCl,Cefetamet |
Others | Others |
Cefetamet is a potent antibiotic to treat respiratory and urinary tract infections. | |||
T30790 |
Ceftolozane sulfate
FR 264205,FR264205,FR-264205 |
Others | Others |
Ceftolozane Sulfate may be used to treat urinary tract infections. | |||
T60260 |
Phenazopyridine
|
Others | Others |
Phenazopyridine 对尿路具有局部镇痛作用,常用于缓解泌尿道感染、手术或泌尿道损伤引起的疼痛、刺激、不适或尿急。 | |||
T30737 |
Carbavance
Meropenem/vaborbactam,Vabomere |
Others | Others |
Carbavance, a mixture of Meropenham and Vaborbactam, is intended for adults with complex urinary tract infections (cUTI), including pyelonephritis, a kidney infection caused by certain bacteria. | |||
T34776 |
Talampicillin
|
Others | Others |
Talampicillin is an ester of Ampicillin. It is hydrolyzed upon absorption to release ampicillin. It is well absorbed from the gastrointestinal tract resulting in a greater bioavailability of ampicillin than can be achieved with equivalent doses of ampicil | |||
T26950 |
Carfecillin Sodium
Carbenicillin Phenyl Sodium,Uticillin,BRL-3475,BRL3475,BRL 3475 |
Others | Others |
Carfecillin Sodium is the phenyl ester of Carbenicillin, it is broken down in the intestinal mucosa to the active antibacterial upon oral administration. Carfecillin Sodiumis used for urinary tract infections. | |||
T40295 |
Carindacillin sodium
Carindacillin sodium,CP-15464-2,Carbenicillin indanyl sodium |
Others | Others |
Carindacillin sodium, also known as Carbenicillin indanyl sodium, is an orally active, broad-spectrum antimicrobial agent. In vivo, it undergoes hydrolysis to Carbenicillin. Carindacillin sodium is specifically utilized in urinary tract infection research. | |||
T68999 |
Cefonicid (free base)
|
Others | Others |
Cefonicid (free base) is a second-generation cephalosporin administered intravenously or intramuscularly. Its bactericidal action results from inhibition of cell wall synthesis. It is used for urinary tract infections, lower respiratory tract infections, and soft tissue and bone infections. | |||
T68817 |
Cefonicid monosodium
|
Others | Others |
Cefonicid monosodium is the salt form of Cefonicid (free base), a second-generation cephalosporin administered intravenously or intramuscularly. Its bactericidal action results from inhibition of cell wall synthesis. It is used for urinary tract infections, lower respiratory tract infections, and soft tissue and bone infections. | |||
T25325 |
Dicyclonon
LAB 145-138H,BAS 145-138 |
Others | Others |
Dicyclonon is a muscarinic antagonist utilized as an antispasmodic and in urinary incontinence. It has little effect on glandular secretion or the cardiovascular system. It has some local anesthetic properties and is utilized in biliary, gastrointestinal, | |||
T69363 |
Emepronium bromide
|
Others | Others |
Emepronium bromide is an anticholinergic drug used in urology as an antispasmodic. It can cause ulceration of esophagus, so it should be taken in orthostatic position with sufficient amounts of liquids. It is a muscarinic antagonist used mainly in the treatment of urinary syndromes. It is incompletely absorbed from the gastrointestinal tract and does not cross the blood-brain barrier. | |||
T39862 |
Trimethoprim lactate
|
Others | Others |
Trimethoprim lactic is a bacteriostatic antibiotic and an orally active dihydrofolate reductase inhibitor. Trimethoprim lactic is active against a wide range of Gram-positive and Gram-negative aerobic bacteria . Trimethoprim lactic has the potential for urinary tract infections, Shigellosis and Pneumocystis pneumonia treatment. | |||
T21677 |
Temafloxacin (hydrochloride)
|
||
Temafloxacin (hydrochloride) 是一种抗生素和抗分枝杆菌剂。 它用于治疗下呼吸道感染、生殖器和泌尿道感染(如前列腺炎)和皮肤感染。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9599 |
3,4,5-Trimethoxybenzaldehyde
|
Anti-infection; Antibacterial | Microbiology/Virology |
3,4,5-Trimethoxybenzaldehyde 是合成各种药物,特别是治疗细菌感染的甲氧苄啶的中间体,它有抗念珠菌功效并抑制粘附和生物膜。 | |||
T1313 |
Nitrofurantoin
Furadantine,呋喃妥因,Macrodantin,Furadonine |
Antibacterial; Antibiotic | Microbiology/Virology |
Nitrofurantoin (Furadantine) 是一种具有口服活性的广谱内酰胺酶抗菌剂。它是一种抗生素,可研究尿路感染。 | |||
T1153 |
Trimethoprim
NIH 204,BW 56-72,甲氧苄啶,NSC-106568 |
DHFR; DNA/RNA Synthesis; Antifolate; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Trimethoprim (NSC-106568) 是抑菌抗生素,也是具有口服活性的二氢叶酸还原酶抑制剂。它对多种革兰氏阳性和革兰氏阴性需氧细菌具有活性,可用于尿路感染,肺孢子菌肺炎和志贺氏菌病的研究。 | |||
T16542 |
Piromidic acid
吡咯酸,吡乙酸三氮萘 |
Antibacterial; Antibiotic | Microbiology/Virology |
Piromidic acid 是一种抗菌剂。它对革兰氏阴性菌和葡萄球菌具有活性,可研究肠道,泌尿和胆道感染。 | |||
T6567 |
Levofloxacin
Levaquin,Cravit,Tavanic,Fluoroquinolone,左氧氟沙星,(-)-Ofloxacin |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Levofloxacin (Fluoroquinolone) 是合成的氟喹诺酮类抗生素,有抑制细菌DNA 旋转酶的超螺旋活性的作用,能阻止DNA 复制。 | |||
T4816 |
6-Hydroxynicotinic acid
6-Hydroxypyridine-3-carboxylic acid,6-羟基烟酸,2-Hydroxy-5-pyridinecarboxylic acid |
Others; Endogenous Metabolite | Metabolism; Others |
6-Hydroxynicotinic acid (6-Hydroxypyridine-3-carboxylic acid) 用于核磁共振波谱或气相色谱-质谱法诊断尿路感染中的铜绿假单胞菌。在引起尿液感染的常见细菌中,只有铜绿假单胞菌从烟酸中产生6-羟基烟酸。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-02832 |
Serpin A5 Protein, Mouse, Recombinant (His)
Protein C inhibitor,Plasminogen activator inhibitor 3,Serpin... |
Mouse | Baculovirus Insect Cells |
Heparin-dependent serine protease inhibitor acting in body fluids and secretions. Inactivates serine proteases by binding irreversibly to their serine activation site. Involved in the regulation of intravascular and extravascular proteolytic activities. Plays hemostatic roles in the blood plasma. Acts as a procoagulant and proinflammatory factor by inhibiting the anticoagulant activated protein C factor as well as the generation of activated protein C factor by the thrombin/thrombomodulin comple... | |||
TMPH-02046 |
Ribonuclease 7 Protein, Human, Recombinant (His)
RNASE7,Skin-derived antimicrobial protein 2,Ribonuclease 7 |
Human | E. coli |
Exhibits a potent RNase activity. Has broad-spectrum antimicrobial activity against many pathogenic microorganisms and remarkably potent activity (lethal dose of 90% < 30 nM) against a vancomycin resistant Enterococcus faecium. Causes loss of bacterial membrane integrity. Probably contributes to urinary tract sterility. Bactericidal activity is independent of RNase activity. Ribonuclease 7 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted... | |||
TMPK-00967 |
DSG-2/Desmoglein-2 Protein, Human, Recombinant (His)
CMD1BB,Desmoglein-2,ARVC10,CDHF5,MGC117037,MGC117036,HDGC,DS... |
Human | HEK293 Cells |
Desmoglein-2 (DSG-2) as the primary high-affinity receptor used by adenoviruses Ad3, Ad7, Ad11 and Ad14. These serotypes represent key human pathogens causing respiratory and urinary tract infections. In epithelial cells, adenovirus binding of DSG-2 triggers events reminiscent of epithelial-to-mesenchymal transition, leading to transient opening of intercellular junctions. DSG-2/Desmoglein-2 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with C-His tag. The predicted mo... | |||
TMPK-00736 |
DSG-2/Desmoglein-2 Protein, Mouse, Recombinant (His)
MGC117036,HDGC,Desmoglein-2,CDHF5,DSG2,MGC117037,ARVC10,CMD1... |
Mouse | HEK293 Cells |
Desmoglein-2 (DSG-2) as the primary high-affinity receptor used by adenoviruses Ad3, Ad7, Ad11 and Ad14. These serotypes represent key human pathogens causing respiratory and urinary tract infections. In epithelial cells, adenovirus binding of DSG-2 triggers events reminiscent of epithelial-to-mesenchymal transition, leading to transient opening of intercellular junctions. DSG-2/Desmoglein-2 Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with C-His tag. The predicted mo... | |||
TMPY-04318 |
GRIK2 Protein, Human, Recombinant (hFc)
GLUR6,EAA4,MRT6,GLR6,glutamate receptor, ionotropic, kainate... |
Human | HEK293 Cells |
GRIK2 (Glutamate Ionotropic Receptor Kainate Type Subunit 2, also known as GluR6) is a Protein Coding gene. The GRIK2 (one of the kainate receptors) gene resides in a genetic linkage region (6q21) associated with bipolar disorder (BPD). The gene coding for GRIK2 has been suggested as a candidate gene for autism based on its localization in the autism-specific region on chromosome 6q21 and the involvement of receptor protein in cognitive functions like learning and memory. GRIK2 belongs to the gl... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TMIJ-0158 |
Sitafloxacin-d4
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Sitafloxacin-d4 是 Sitafloxacin 的氘代化合物。Sitafloxacin 的 CAS 号为 127254-12-0。Sitafloxacin (Sitafloxacin anhydrous) 是一种具有口服活性的氟喹诺酮类抗生素,具有广谱的抗菌活性。Sitafloxacin 可用于研究呼吸道感染和尿路感染。 | |||
T36537 |
Nitrofurantoin-13C3
Nitrofurantoin-13C3 |
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Nitrofurantoin-13C3is intended for use as an internal standard for the quantification of nitrofurantoin by GC- or LC-MS. Nitrofurantoin is a nitrofuran antibiotic.1In vivo, nitrofurantoin (25-100 mg/kg) reducesE. colireplication and abscess formation in the renal medulla of infected rats in a dose-dependent manner. It prevents kidney and bladder infection in rats following bladder inoculation with clinical isolates ofP. mirabilis. Nitrofurantoin also prevents alkalization of urine, as well as ca... | |||
TMIJ-0437 |
Sulfameter-d4
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Sulfameter-d4 是 Sulfameter 的氘代化合物。Sulfameter 的 CAS 号为 651-06-9。Sulfameter是一种长效磺胺类抗生素,具有抗菌活性。它可研究尿路感染和麻风病。 | |||
TMIH-0532 |
Sulfachloropyridazine-d4
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Sulfachloropyridazine-d4 是 Sulfachloropyridazine 的氘代化合物。Sulfachloropyridazine 的 CAS 号为 80-32-0。Sulfachloropyridazine 是一种广谱磺酰胺,抑制革兰氏阳性和革兰氏阴性好氧细菌的生长。 | |||
TMID-0195 |
Levofloxacin-d8
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Levofloxacin-d8 是 Levofloxacin 的氘代化合物。Levofloxacin 的 CAS 号为 100986-85-4。Levofloxacin是合成的氟喹诺酮类抗生素,有抑制细菌DNA旋转酶的超螺旋活性的作用,能阻止DNA复制。 | |||
TMID-0063 |
rac Bendroflumethiazide-d5
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rac Bendroflumethiazide-d5 是 rac Bendroflumethiazide 的氘代化合物。rac Bendroflumethiazide 的 CAS 号为 73-48-3。Bendroflumethiazide 是一种口服具有活性的利尿剂。它是一种抗高血压药。它对动脉高血压疾病具有潜在的研究价值。 | |||
TMIH-0300 |
Levofloxacin-d3
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Levofloxacin-d3 是 Levofloxacin 的氘代化合物。Levofloxacin 的 CAS 号为 100986-85-4。Levofloxacin是合成的氟喹诺酮类抗生素,有抑制细菌DNA旋转酶的超螺旋活性的作用,能阻止DNA复制。 | |||
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... |