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Cat. No. | Product Name | ||
---|---|---|---|
L9410 | 共价抑制剂库 | 1920 compounds | |
1920 种小分子的独特集合,包含已发现的共价抑制剂以及包含某些共价反应基团常见弹头的分子,如氯乙酰基,2-氯丙酰基,丙烯酰基,1-丙-2-炔基,1-丁-2-炔基,酮羰基,二硫键等,可以用于共价抑制剂药物研发; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T8345 |
Carbutamide
|
Others | Others |
Carbutamide 是一代磺酰脲,口服具有活性,具有降血糖作用。 | |||
T6451 |
Clodronic acid disodium salt
Loron,Clodronate Disodium,氯屈膦酸二钠,Lodronate |
Others | Others |
Clodronic acid disodium salt (Lodronate) 是一种口服具有活力的破骨细胞骨吸收 (osteoclastic bone resorption) 的抑制剂,是一代双磷酸盐。它可用于高骨转换状态、Paget’s 病和溶骨性骨转移中。 | |||
T0370 |
Pheniramine maleate
Daneral,Inhiston,Trimetose,马来酸非尼拉敏 |
5-HT Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Pheniramine maleate (Trimetose) 是一种具有抗组胺和血管扩张特性的烷基胺衍生物,可与组胺 H1 受体结合,从而抑制磷脂酶 A2 和内皮源性松弛因子一氧化氮的产生。 | |||
T0141 |
Cephalonium
头孢洛宁,Cefalonium |
Others | Others |
Cephalonium (Cefalonium) 是第一代头孢菌素类抗生素。 | |||
T0141L |
Cefalonium Dihydrate(5575-21-3 free base)
Cefalonium Dihydrate |
Others | Others |
Cefalonium Dihydrate(5575-21-3 free base) 是第一代头孢菌素类抗生素。 | |||
T0371 |
Gliquidone
AR-DF 26,格列喹酮,Glurenorm |
Potassium Channel | Membrane transporter/Ion channel |
Gliquidone (AR-DF 26) 是一种磺酰脲类的抗糖尿病药物,可用于2型糖尿病的研究。 | |||
T9225 |
Vebicorvir
ABI-H0731 |
HBV | Microbiology/Virology |
Vebicorvir (ABI-H0731) 是一种乙型肝炎病毒核心蛋白的抑制剂,有抗病毒活性。 | |||
T8457 |
NPS2390
|
GluR | Neuroscience |
NPS2390 是钙敏感受体抑制剂,也是 mGluR1 和 mGluR5 的非竞争性拮抗剂。 | |||
T0092 |
Antazoline hydrochloride
盐酸安他唑啉,Phenazocine HCl,Phenazoline hydrochloride,Antazoline HCl |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Antazoline hydrochloride (Phenazoline hydrochloride) 是一种抗组胺药,可与组胺H1受体结合,阻断内源性组胺的作用。它也具有抗胆碱能特性,可缓解鼻塞,也可用作眼药水。 | |||
T21419 |
Diphenhydramine
苯海拉明,Debendrin,PM 255,PM255,Dabylen,Syntedril,PM-255 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Diphenhydramine (Syntedril) 是第一代具有抗胆碱能作用的H1 受体拮抗剂,它能透过血脑屏障。 | |||
T0199 |
Cephradine
Anspor,Cephradin,Velosef,SQ-11436,Sefril,头孢拉定 |
TOPK; Antibacterial; Antibiotic | MAPK; Microbiology/Virology |
Cephradine (Anspor) 是广谱口服活性头孢菌素。它对革兰氏阳性和革兰氏阴性病原体都有活性。它已用于泌尿生殖系统、胃肠道和呼吸道感染以及皮肤和软组织感染的研究。它通过直接抑制TOPK 抑制太阳紫外线诱导的皮肤炎症。 | |||
T7941 |
Imipramine hydrochloride
盐酸丙咪嗪,Imipramine (hydrochloride),Tofranil,G 22355,Imipramine HCl,Melipramine |
Serotonin Transporter | Neuroscience |
Imipramine hydrochloride (Imipramine HCl) 可抑制血清素转运蛋白,IC50=32 nM。它可阻止胰酶的易位,阻碍 MV 和外泌体的分泌。 | |||
T0445L |
Promethazine hydrochloride
盐酸异丙嗪,Promethazine HCl,Phenergan |
Adrenergic Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Promethazine hydrochloride (Promethazine HCl) 是抗组胺药物,是 H1 受体的强拮抗剂和 mACh 受体的中度拮抗剂,对 5-HT2A、5-HT2C、D2 和 α1-肾上腺素能受体具有中等亲和力。 | |||
T0059 |
Diphenylpyraline hydrochloride
盐酸双苯比拉林,4-Diphenylmethoxy-1-methylpiperidine hydrochloride |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Diphenylpyraline hydrochloride (4-Diphenylmethoxy-1-methylpiperidine hydrochloride) 是一种组胺 H1 受体的拮抗剂,抑制多巴胺的吸收。它是可口服的抗组胺试剂,具有抗胆碱和抗过敏作用,可用于缓解过敏性疾病,如鼻炎、花粉热和瘙痒性皮肤疾病等。 | |||
T2551 |
Etravirine
TMC125,依曲韦林,R165335 |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Etravirine (R165335) 是一种非核苷逆转录酶抑制剂,具有抗 HIV 的作用。 | |||
T16472 |
Pericyazine
Propericiazine,氰噻嗪,RP 8909 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Pericyazine (Propericiazine) 是第一代抗精神病药物,是一种选择性的 D2 多巴胺受体 (D2-dopamine receptor) 拮抗剂,具有肾上腺溶解、抗胆碱能和锥体外系作用,被用作短期管理严重焦虑状态和精神病的辅助药物。 | |||
T21390 |
Fexofenadine
Carboxyterfenadine,Telfast,非索非那定,MDL 16.455,Allegra |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Fexofenadine (Carboxyterfenadine) 是一种抗组胺药物,用于治疗过敏症状,如鼻塞、花粉热和荨麻疹。与第一代抗组胺药相比,它通过血脑屏障并引起镇静的能力较差。 | |||
T0816 |
Acetohexamide
Acetohexamid,醋磺环已脲,Dymelor,醋磺己脲,Gamadiabet |
Potassium Channel; NADPH | Membrane transporter/Ion channel; Metabolism |
Acetohexamide (Acetohexamid) 是磺脲类试剂,可刺激胰腺分泌胰岛素,能够用于 2 型糖尿病的相关研究。 | |||
T0953 |
Cefazolin sodium
Ancef,头孢唑啉钠,头孢唑林钠,Cefazolin sodium salt,Sodium cephazolin,cephazolin sodium,cefazoline sodium,Sodium cefazolin |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Cefazolin sodium (cephazolin sodium) salt 是一种头孢类抗生素, 可研究多种细菌感染。 | |||
T1122 |
Cephalothin sodium
头孢噻吩钠,Cefalotin sodium,Cephalothin,Cefalotin |
Antibacterial; Antibiotic | Microbiology/Virology |
Cephalothin sodium (Cefalotin) 是一种头孢类抗生素, 具有广泛的抗菌活性,抑制革兰氏阳性和阴性菌。 | |||
T0373 |
Erlotinib
OSI-744,NSC 718781,CP358774,埃罗替尼,R1415 |
EGFR; Autophagy | Angiogenesis; Autophagy; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Erlotinib (CP358774) 是一种 EGFR 一代抑制剂,抑制 EGFR 19 Del 和 L858R 突变。Erlotinib 具有抗肿瘤活性,用于治疗 EGFR 突变的非小细胞肺癌。Erlotinib 用药会产生 EGFR C797S 耐药突变。 | |||
T68967 |
AFG206
|
Others | Others |
AFG206 is the novel first-generation type II" FLT3 inhibitor." | |||
T0059L |
Diphenylpyraline
Difenilpiralina,AN 1041,AN1041,Dayfen,AN-1041,二苯拉林 |
Others | Others |
Diphenylpyridine is the first generation antihistamine, which has the anticholinergic effect of diphenylpiperidine. | |||
T33319 |
Methdilazine Hydrochloride
Bristaline,Dilosyn,Methdilazine Hcl,Tacaryl hydrochloride,Disyncran |
Others | Others |
Methdilazine Hydrochloride is a first-generation phenothiazine class antihistamine with anticholinergic properties. | |||
T14929 |
Cephradine monohydrate
头孢拉定一水合物,Cefradine monohydrate |
Antibacterial | Microbiology/Virology |
Cephradine monohydrate, a first-generation cephalosporin, is active against a wide range of Gram-positive and Gram-negative bacteria. | |||
T0445L1 |
Promethazine hibenzate
D-08768,D08768,D 08768 |
Others | Others |
Promethazine is a neuroleptic medication and first-generation antihistamine of the phenothiazine family. | |||
T32233 |
Isothipendyl
Udantol,Isothipendylum,Odantol,Andanton,Nilergex |
Others | Others |
Isothipendyl is the first generation of H1 antagonists (antihistamines) and anticholinergics and has an effect on itching. | |||
T20616 |
Coumachlor
G-23133,Ratilan,G23133,Tomorin,G 23133 |
Others | Others |
Coumachlor, a first-generation anticoagulant rodenticide, blocks the formation of prothrombin and inhibits blood coagulation causing internal haemorrhage. | |||
T70308 |
PLX7683
|
Others | Others |
PLX7683 is a paradox breaker. Paradox breakers overcame several known mechanisms of resistance to first-generation RAF inhibitors. Dissociating MAPK pathway inhibition from paradoxical activation might yield both improved safety and more durable efficacy than first-generation RAF inhibitors | |||
T69702 |
AFG210
|
Others | Others |
AFG210 is a novel first-generation “type II” FLT3 inhibitor. | |||
T71117 |
AZD5248
|
Others | Others |
AZD-5248 is a potent, selective, first generation, oral inhibitor of dipeptidyl peptidase 1 (DPP1). | |||
T38918 |
Revusiran
ALN-TTRSC |
Others | Others |
Revusiran (ALN-TTRSC) is a first-generation short interfering RNA (siRNA) that specifically targets transthyretin (TTR) mRNA. It is utilized in TTR-mediated amyloidosis research. | |||
T40591 |
Verapamil EP Impurity C hydrochloride
NSC-609249 hydrochloride |
Others | Others |
NSC-609249 hydrochloride, an impurity of Verapamil, is a calcium channel blocker with potent orally active properties. It also functions as a first-generation P-glycoprotein (P-gp) inhibitor. | |||
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. | |||
T32700 |
Levocabastine
Livostin,Bilina |
Others | Others |
Levocarbastine is a second-generation H1 receptor antagonist for allergic conjunctivitis. It also acts as a potent selective antagonist for the neurotensin receptor NTS2 and is the first drug to be used to characterize different neurotensin subtypes. | |||
T14040 |
4-Hydroxytolbutamide
Hydroxytolbutamide |
Potassium Channel | Membrane transporter/Ion channel |
4-Hydroxytolbutamide(Hydroxytolbutamide), a metabolite of Tolbutamide, which is metabolized by CYP2C8 and CYP2C9. Tolbutamide is a first generation potassium channel blocker and a sulfonylurea oral antidiabetic[1][2]. | |||
T19979 |
Saccharin sodium hydrate
O-benzoic sulfimide sodium salt,糖精钠,Saccharin, sodium salt hydrate |
Others | Others |
Saccharin, sodium salt hydrate is used in the food industry and for sweetening diabetes diet. It is also used as a synthetic sweet ignorance agent. Saccharin, sodium salt hydrate is the first generation′ synthetic sugar alternative that has been studied f | |||
T19678 |
Cefaloridine
Cephaloridine,Sch 11527 |
Others | Others |
Cefaloridine is a first-generation semisynthetic derivative of cephalosporin C. It is unique among cephalosporins in that it exists as a zwitterion. Cephaloridine was very effective to cure pneumococcal pneumonia. It has a high clinical and bacteriologica | |||
T36211 |
16(R)-Iloprost
|
Others | Others |
Iloprost is a second generation structural analog of prostacyclin (PGI2) with about ten-fold greater potency than the first generation stable analogs, typified by carbaprostacyclin. Iloprost binds with equal affinity to the recombinant human IP and EP1 receptors with a Ki value of 11 nM. Most preparations of iloprost contain 16(S) and 16(R) stereoisomers. 16(R)-Iloprost inhibits platelet aggregation with an IC50 value of 65 nM. | |||
T36212 |
16(S)-Iloprost
|
Others | Others |
Iloprost is a second generation structural analog of prostacyclin (PGI2) with about ten-fold greater potency than the first generation stable analogs, typified by carbaprostacyclin. Iloprost binds with equal affinity to the recombinant human IP and EP1 receptors with a Ki value of 11 nM. Most preparations of iloprost contain 16(S) and 16(R) stereoisomers. 16(S)-Iloprost potently inhibits platelet aggregation with an IC50 value of 3.5 nM. | |||
TP2288 |
Rapalink-1
|
Others | Others |
RapaLink-1 is the third-generation mTOR inhibitor exploiting the unique juxtaposition of two drugs (first- and second-generation mTOR kinase inhibitors) -binding pockets to create a bivalent interaction that allows inhibition of the mutants which has resi | |||
T71577 |
KOS-1584
|
Others | Others |
KOS-1584 is a second-generation epothilone with potential antineoplastic activity. Epothilone KOS-1584 binds to tubulin and induces microtubule polymerization and stabilizes microtubules against depolymerization, which may result in the inhibition of cell division, the induction of G2/M arrest, and apoptosis. Compared to first-generation epothilones, this agent exhibits greater safety and efficacy with an enhanced pharmaceutical profile, including enhanced water solubility and tumor penetration,... | |||
T75300 |
Cefazolin sodium pentahydrate
|
Others | Others |
Cefazolin sodium pentahydrate 是一代头孢菌素类抗生素,可用于多种细菌感染的研究。Cefazolin sodium pentahydrate 具有抗炎作用,可以减轻术后认知功能障碍 (POCD)。 | |||
T35619 |
Dapagliflozin-3-O-β-D-Glucuronide
|
Others | Others |
Dapagliflozin-3-O-β-D-glucuronide is a metabolite of dapagliflozin . Dapagliflozin is a first generation selective sodium glucose cotransporter (SGLT) 2 inhibitor that blocks glucose transport.[1] Dapagliflozin is metabolized by uridine diphosphate glucuronosyltransferase (UGT) 1A9 to dapagliflozin-3-O-β-D-glucuronide, which is 2,600-fold less potent than the parent compound with regard to SGLT2 inhibition.[2] | |||
T0366L |
Cefadroxil (hydrate)
|
Others | Others |
Cefadroxil is a first generation aminocephalosporin with good patient compliance, a long-acting therapeutic effect, high solubility and relatively broad spectrum of anti-bacterial activity. Cefadroxil is also a substrate of the intestinal peptide transporter PepT1, which is primarily responsible for the drug's uptake across the apical membrane of small intestine. | |||
T71110 |
Nanatinostat TFA
|
Others | Others |
Nanatinostat, also known as Tractinostat, CHR-3996 and VRx-3996, is an orally bioavailable, second-generation hydroxamic acid-based inhibitor of histone deacetylase (HDAC) with potential antineoplastic activity. HDAC inhibitor CHR-3996 inhibits HDAC, resulting in an accumulation of highly acetylated histones, the induction of chromatin remodeling, and the selective transcription of tumor suppressor genes; these events may result in the inhibition of tumor cell division and the induction of tumor... | |||
T69925 |
NVR3-778 hydrate
|
Others | Others |
NVR 3-778 is the first capsid assembly modulator (CAM) that has demonstrated antiviral activity in hepatitis B virus (HBV)-infected patients. NVR 3-778 inhibited the generation of infectious HBV DNA-containing virus particles with a mean antiviral 50% effective concentration (EC50) of 0.40 µM in HepG2.2.15 cells. The antiviral profile of NVR 3-778 indicates pan-genotypic antiviral activity and a lack of cross-resistance with nucleos(t)ide inhibitors of HBV replication. | |||
T70287 |
BMS-186511
|
Others | Others |
BMS-186511 is a Farnesyltransferase (FT) inhibitor with potential anticancer activity. BMS-186511 is a bisubstrate analogue inhibitor of FT, would inhibit the malignant growth properties of a cell line established from malignant schwannoma of an NF1 patient. Following treatment with BMS-186511 , ST88-14 cells became flat, nonrefractile, were contact-inhibited, and lost their ability to grow in soft agar. BMS-186511 was found to specifically inhibit FT, but not geranylgeranyltransferase I, a clos... | |||
T36175 |
AAPH
|
Others | Others |
AAPH is a water-soluble azo compound which is used extensively as a free radical generator, often in the study of lipid peroxidation and the characterization of antioxidants.[1],[2],[3],[4] Decomposition of AAPH produces molecular nitrogen and 2 carbon radicals. The carbon radicals may combine to produce stable products or react with molecular oxygen to give peroxyl radicals. The half-life of AAPH is about 175 hours (37°C at neutral pH), making the rate of free radical generation essentially con... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8063 |
Cephapirin Benzathine
|
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Cephapirin Benzathine 是头孢哌啶的苄硫醚盐形式,是一种广谱抗生素。 | |||
T8062 |
Cefazedone
Refosporen,头孢西酮 |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Cefazedone (Refosporen) 是一种具有抗革兰氏阳性和革兰氏阴性菌活性的时间依赖性头孢菌素抗生素。 | |||
T1004 |
6-Benzylaminopurine
6-苄氨基嘌呤,6-BAP,N6-Benzyladenine,BA,Benzyladenine |
Others | Others |
6-Benzylaminopurine (6-BAP) 是一种细胞分裂素,能够通过刺激细胞分裂引起植物生长和发育,抑制呼吸激酶,从而延长绿色蔬菜的保鲜。 | |||
T1181 |
Gefitinib
ZD1839,吉非替尼 |
EGFR; Tyrosine Kinases; Autophagy | Angiogenesis; Autophagy; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Gefitinib (ZD1839) 是一种 EGFR 一代抑制剂,具有口服活性,抑制 EGFR 19 Del 和 L858R 突变。Gefitinib 具有抗肿瘤活性,用于治疗 EGFR 突变的非小细胞肺癌。Gefitinib 用药会产生 EGFR C797S 耐药突变。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-00585 |
Beta-lactamase CTX-M-1 Protein, E. coli, Recombinant (Yeast, His)
Beta-lactamase MEN-1,Cefotaximase 1,bla,men1,Beta-lactamase ... |
E. coli | P. pastoris (Yeast) |
Broad spectrum beta-lactamase which confers resistance to penicillins, as well as first, second and third-generation cephalosporins. | |||
TMPH-00584 |
Beta-lactamase CTX-M-1 Protein, E. coli, Recombinant (His)
men1,Beta-lactamase MEN-1,Cefotaximase 1,Beta-lactamase CTX-... |
E. coli | E. coli |
Broad spectrum beta-lactamase which confers resistance to penicillins, as well as first, second and third-generation cephalosporins. | |||
TMPH-03106 |
Coagulation factor XII Protein, Pig, Recombinant (His)
HAF,Hageman factor,F12,Coagulation factor XII |
Sus scrofa (Pig) | E. coli |
Factor XII is a serum glycoprotein that participates in the initiation of blood coagulation, fibrinolysis, and the generation of bradykinin and angiotensin. Prekallikrein is cleaved by factor XII to form kallikrein, which then cleaves factor XII first to alpha-factor XIIa and then trypsin cleaves it to beta-factor XIIa. Alpha-factor XIIa activates factor XI to factor XIa. Coagulation factor XII Protein, Pig, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predic... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIJ-0523 |
Gliquidone-d6
|
||
Gliquidone-d6 是 Gliquidone 的氘代化合物。Gliquidone 的 CAS 号为 33342-05-1。Gliquidone 是一种磺酰脲类的抗糖尿病药物,可用于2型糖尿病的研究。 |