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T3639A-804598A 804598;A804598
A-804598 is a competitive and selective P2X7 receptor antagonist (IC50: 10 nM, rat; 9 nM, mouse; 11 nM, human).
价 格:¥电议型 号:T3639产 地:中国大陆
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T3599BFH772BFH-722
BFH772, a structure analogue of BAW2881, is a potent and selective VEGF inhibitor. BFH772 is highly effective at targeting VEGFR2 kinase with an IC50 value of 3 nM. BFH772 inhibits the ligand induced autophosphorylation of RET, PDGFR, and KIT kinases, wit
价 格:¥电议型 号:T3599产 地:中国大陆
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T3598JNK-IN-7JNK inhibitor
JNK-IN-7 is a selective JNK1/2/3 inhibitor (IC50: 1.54/1.99/0.75 nM). It can also inhibit phosphorylation of c-Jun, which is a substrate of JNK kinase.
价 格:¥电议型 号:T3598产 地:中国大陆
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T3597Cutamesine dihydrochloride库他美新二盐酸盐;SA4503 (dihydrochloride);AGY94806 dihydrochloride;SA4503 dihydroc
Cutamesine dihydrochloride is a selective σ1 receptor agonist (IC50: 17.4 nM). It shows selectivity for σ1 over σ2 receptors, and inhibits angiotensin II-induced cardiomyocyte hypertrophy in vitro and attenuates myocardial hypertrophy in vivo. In a rat mo
价 格:¥电议型 号:T3597产 地:中国大陆
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T35951Alkaline Phosphatase
Alkaline Phosphatase is an ubiquitous membrane-bound glycoprotein that catalyzes the hydrolysis of phosphate monoesters at basic pH values.
价 格:¥电议型 号:T35951产 地:中国大陆
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T3595ResmetiromVIA-3196;MGL3196
MGL-3196 is a highly selective thyroid hormone receptor β (THR-β) agonist.
价 格:¥电议型 号:T3595产 地:中国大陆
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T3593Src Inhibitor 1Src Kinase Inhibitor 1;Src-l1
Src Inhibitor 1 is a potent and selective dual site Src tyrosine kinase inhibitor.
价 格:¥电议型 号:T3593产 地:中国大陆
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T3592MQAE
MQAE, a fluorescent chloride ion indicator, is more sensitive and selective than 36Cl and microelectrode-based methods for chloride measurement in cells. MQAE is quenched via collision with chloride.
价 格:¥电议型 号:T3592产 地:中国大陆
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T3591URB602
URB602 is a specific monoacylglycerol lipase (MGL) inhibitor, which inhibits rat brain MGL (IC50: 28±4 μM) through a noncompetitive mechanism.
价 格:¥电议型 号:T3591产 地:中国大陆
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T35900JAK2-IN-7JAK2-IN-7
JAK2-IN-7 is a selective JAK2 inhibitor with IC50s of 3, 11.7, and 41 nM for JAK2, SET-2, and Ba/F3V617F cells, respectively. JAK2-IN-7 possesses >14-fold selectivity over JAK1, JAK3, FLT3. JAK2-IN-7 stimulates cell cycle arrest in the G0/G1 phase and ind
价 格:¥电议型 号:T35900产 地:中国大陆
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T3590NSC23005
NSC23005 sodium is a p18INK inhibitor with potently promoted hematopoietic stem cell (HSC) expansion (ED50: 5.21 nM).
价 格:¥电议型 号:T3590产 地:中国大陆
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T35594-Oxoisotretinoin4-Oxoisotretinoin;Oxoretinoic acid;Ro 22-6595
4-oxo-isotretinoin is the major blood metabolite.
价 格:¥电议型 号:T3559产 地:中国大陆
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T3530Otenabant奥替那班;CP-945598
Otenabant has been investigated for the treatment of Obesity.
价 格:¥电议型 号:T3530产 地:中国大陆
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T3497OcaperidoneR79598;Ocaperidona;奥卡哌酮
Ocaperidona (Ocaperidone), a very high affinity dopamine D2 antagonist.
价 格:¥电议型 号:T3497产 地:中国大陆
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T3485ProbimaneMM-159;AT-2153
Probimane had Anti-proliferative effects, cell cycle G2/M phase arrest and blocking of chromosome segregation in human tumor cell lines with MST-16.
价 格:¥电议型 号:T3485产 地:中国大陆
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T3459VK3-OCH32-[(2-Methoxy)ethylthio]-3-methyl-1,4-na
2-[(2-Methoxy)ethylthio]-3-methyl-1,4-na is a selective antitumor agent via heme oxygenase (HO-1) related mechanisms; Vitamine K3 analogue.
价 格:¥电议型 号:T3459产 地:中国大陆
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T34532Sari 59-801Sari-59-801
Sari 59-801 is a novel, orally effective hypoglycemic compound that appears to act largely by stimulation of insulin release. SARI-59-801 was more potent in producing hypoglycemia (ED25 = 47 mg/kg) than their lean littermates (ED25 = 131 mg/kg).
价 格:¥电议型 号:T34532产 地:中国大陆
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T3366Cephalotaxine三尖杉碱;Cephalotaxlen;ZINC19795976;(-)-Cephalotaxine
Cephalotaxine is an antiviral and an antitumor agent.
价 格:¥电议型 号:T3366产 地:中国大陆