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T35328H-1152 dihydrochlorideH 1152 dihydrochloride,H1152 dihydrochloride
H-1152 dihydrochloride is a specific inhibitor of Rho-associated protein kinase (ROCK) with an IC50 of 12 nM and a Ki of 1.6 nM. H-1152 dihydrochloride inhibits PKA, PKC, PKG, Aurora A and CaMKII with IC50 values of 3.03 μM, 5.68 μM, 0.360 μM, 0.745 μM and 0.180 μM, respectively.
价 格:¥电议型 号:T35328产 地:中国大陆
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T2602Barasertib-HQPABarasertib;AZD1152-HQPA;1H-Pyrazole-3-acetamide;AZD2811;AZD1152-HQPA|AZD2811
Barasertib (AZD1152-HQPA) is a highly selective Aurora B inhibitor (IC50: 0.37 nM) and demonstrates ~3,700-fold greater selectivity than Aurora A.
价 格:¥电议型 号:T2602产 地:中国大陆
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T22383NSC 31152NSC 102533;5-(4-Chloro-benzylidene)-thiazolidine-2,4-dione
NSC 31152 is a bioactive chemical.
价 格:¥电议型 号:T22383产 地:中国大陆
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T2134Dorzolamide hydrochloride盐酸多佐胺;Dorzolamide HCl;MK507 hydrochloride;L671152 hydrochloride;MK-507 (L-6
Dorzolamide Hydrochloride is the hydrochloride salt form of dorzolamide, an inhibitor of carbonic anhydrase, a zinc-containing enzyme that catalyzes the rapid conversion of carbon dioxide and water into carbonic acid, protons and bicarbonate ions. Distrib
价 格:¥电议型 号:T2134产 地:中国大陆
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T21152Ac-Phe-NH2Ac Phe NH2;Ac Phe-NH2;Ac-Phe NH2
Ac-Phe-NH2 is a non-competitive inhibitor of polyubiquitin chain elongation at Ki value of 8 ± 1.2 mM.
价 格:¥电议型 号:T21152产 地:中国大陆
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T13467(±)-Enitociclib(±)-BAY-1251152
(±)-BAY-1251152 is a racemic mixture of BAY-1251152. BAY-1251152 is highly selective inhibitor of PTEF/CDK9.
价 格:¥电议型 号:T13467产 地:中国大陆
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T11529H3B-120
H3B-120 is a highly selective, competitive, and allosteric carbamoyl phosphate synthetase 1 (CPS1) inhibitor (IC50: 1.5 μM; Ki: 1.4 μM) with anti-cancer activity.
价 格:¥电议型 号:T11529产 地:中国大陆
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T11527LH-Ser-His-OH acetate
H-Ser-His-OH acetate is an endogenous metabolite hydrolysis cleavage activity.
价 格:¥电议型 号:T11527L产 地:中国大陆
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T11526DPP-IV-IN-2H-Lys(4-nitro-Z)-pyrrolidide
DPP-IV-IN-2 is an inhibitor of both DP8/9?and dipeptidyl peptidase IV (IC50s: 0.1 and 0.95 μM).
价 格:¥电议型 号:T11526产 地:中国大陆
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T11520GW806742X
GW806742X is an inhibitor of Mixed Lineage Kinase Domain-Like protein (MLKL) which binds the MLKL pseudokinase domain (Kd: 9.3 μM) with anti-necroptosis activity. GW806742X has activity against VEGFR2.
价 格:¥电议型 号:T11520产 地:中国大陆
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T1152Albendazole阿苯达唑;SKF-62979
Albendazole is used as a drug indicated for the treatment of a variety of worm infestations.
价 格:¥电议型 号:T1152产 地:中国大陆
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T1152AlbendazoleAlbendazole,SKF-62979,
Albendazole is used as a drug indicated for the treatment of a variety of worm infestations.
价 格:¥电议型 号:T1152产 地:美洲
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T11520GW806742XGW806742X
GW806742X has activity against VEGFR2.?GW806742X is a Mixed Lineage Kinase Domain-Like protein (MLKL) inhibitor which binds the MLKL pseudokinase domain with a Kd value of 9.3 μM and has anti-necroptosis activity.?
价 格:¥电议型 号:T11520产 地:美洲
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T11521GW 766994GW 766994,GW 994,
GW 766994 has has the potential for asthma and eosinophilic bronchitis treatment.GW 766994 is a specific and oral chemokine receptor-3 (CCR3) antagonist.
价 格:¥电议型 号:T11521产 地:美洲
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T11525GW311616GW311616
GW-311616 is a orally bioavailable,potent , long duration and selective human neutrophil elastase (HNE) inhibitor with IC50 value of 22 nM and Ki value of 0.31 nM.
价 格:¥电议型 号:T11525产 地:美洲
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T11525LGW311616 hydrochlorideGW311616 hydrochloride,GW311616A,
GW-311616 is a potent, long duration,orally bioavailable and selective human neutrophil elastase (HNE) inhibitor with IC50 value of 22 nM and Ki value of 0.31 nM.
价 格:¥电议型 号:T11525L产 地:美洲
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T11526DPP-IV-IN-2DPP-IV-IN-2
DPP-IV-IN-2 is an inhibitor of both DP8/9?and dipeptidyl peptidase IV (DPIV) ?with IC50s of 0.1 and 0.95 μM, respectively.
价 格:¥电议型 号:T11526产 地:美洲
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T13420(-)-BAY-1251152(-)-BAY-1251152
(-)-BAY-1251152 is an enanthiomer of BAY-1251152 with rotation (-). BAY-1251152 is a potent and highly selective inhibitor of PTEF/CDK9.
价 格:¥电议型 号:T13420产 地:美洲
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T13467(±)-BAY-1251152(±)-BAY-1251152
(±)-BAY-1251152 is a racemic mixture of BAY-1251152. BAY-1251152 is highly selective inhibitor of PTEF/CDK9.
价 格:¥电议型 号:T13467产 地:美洲
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T14371AZD1152AZD1152,Barasertib,
AZD1152 is a pro-drug of Barasertib-hQPA. Which is a highly selective Aurora B inhibitor with IC50 of 0.37 nM in a cell-free assay.
价 格:¥电议型 号:T14371产 地:美洲