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T29530ABT-515；化合物 T29530ABT 515|||UNII-186W5U73P9；ABT 515|||UNII-186W5U73P9
ABT-515 is a bio-active chemical. Detailed information has not been published.
价 格：￥电议型 号：T29530产 地：中国大陆
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T294736-Hydroxyadenosine；化合物 T294736-Hydroxyadenosine
6-Hydroxyadenosine can protect cells from apoptosis.
价 格：￥电议型 号：T29473产 地：中国大陆
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T294073-Hydroxydecanedioic acid；化合物 T294073-Hydroxydecanedioic acid
3-hydroxydecanedioic acid can be found in ketoacidosis of urinary metabolites.
价 格：￥电议型 号：T29407产 地：中国大陆
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T293973-Ethylphenyl etaqualone；化合物 T293973-Ethylphenyl etaqualone
3-Ethylphenyl etaqualone is a bioactive chemical.
价 格：￥电议型 号：T29397产 地：中国大陆
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T293873-Azabicyclo(3.2.1)octane, N,2,4-trimethyl-；化合物 T293873-Azabicyclo(3.2.1)octane, N,2,4-trimethyl-
3-Azabicyclo(3.2.1)octane, N,2,4-trimethyl- is a Drug / Therapeutic Agent.
价 格：￥电议型 号：T29387产 地：中国大陆
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T293732-Pyridineacetamide, 5-methylthio-；化合物 T29373AG 42|||AG-42 AG42；AG 42|||AG-42 AG42
2-Pyridineacetamide, 5-methylthio- is a biochemical.
价 格：￥电议型 号：T29373产 地：中国大陆
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T292731,3-Bis(3-phenoxyphenoxy)benzene；化合物 T292731,3-Bis(3-phenoxyphenoxy)benzene
1,3-Bis(3-phenoxyphenoxy)benzene is a bioactive chemical.
价 格：￥电议型 号：T29273产 地：中国大陆
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T29221(R)-ZINC-3573化合物 (R)-ZINC-3573ZINC 3573
(R)-ZINC-3573 is a potent and highly selective MRGPRX2 probe. (R)-ZINC-3573 activates endogenous MRGPRX2 in a human mast cell line, inducing degranulation and calcium release.
价 格：￥电议型 号：T29221产 地：中国大陆
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T29212ZD-8731 HCl；化合物 T29212ZD 8731|||ZD-8731|||ZD-8731 hydrochloride|||ZD8731|||ICI-D 8731|||ICI-D-8731；Z
ZD-8731, an angiotensin type 1 receptor antagonist, is used potentially for the treatment of hypertension and heart failure.
价 格：￥电议型 号：T29212产 地：中国大陆
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T29173YF-452；化合物 T29173YF-452
YF-452 inhibits tumor growth through antiangiogenesis by suppressing VEGF receptor 2 signaling.
价 格：￥电议型 号：T29173产 地：中国大陆
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T29136VU0424465；化合物 T29136VU 0424465|||ML273|||ML-273|||VU-0424465|||ML 273；VU 0424465|||ML273|||ML-273|||
VU0424465 is a mGlu5-selective allosteric agonist.
价 格：￥电议型 号：T29136产 地：中国大陆
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T29073UR-2922；化合物 T29073UR2922|||UR-2922|||UR 2922|||UR 2922|||UR2922|||UR 2922；UR2922|||UR-2922|||UR 2922
UR-2922 is an oral antagonist of platelet GPIIb/IIIa. UR-2922 possessed a high affinity for the human platelet receptor (K(d) <1 nM) and a slow dissociation rate (k(off)= 90 min) in vitro. UR-2922 induced no ligand-induced binding sites (LIBS) expression or prothrombotic activity in human platelets.
价 格：￥电议型 号：T29073产 地：中国大陆
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T28973TIBI；化合物 TIBITIBI
TIBI is an ATP-competitive Rio1 inhibitor that acts in a similar manner to fungamycin and enhances the thermal stability of the enzyme.
价 格：￥电议型 号：T28973产 地：中国大陆
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T28873Su 9055；化合物 T28873Su-9055|||Su9055；Su-9055|||Su9055
Su 9055 is an antagonist of adrenal cortex hormone.
价 格：￥电议型 号：T28873产 地：中国大陆
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T28858SSR504734；化合物 T28858SSR-504734|||SSR 504734；SSR-504734|||SSR 504734
SSR504734 is a novel potent glycine transporter 1 (GlyT1) inhibitor.
价 格：￥电议型 号：T28858产 地：中国大陆
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T28847SR-17398；化合物 T28847SR-17398
SR-17398 is an inhibitor of Unc-51-Like Kinase 1 (ULK1) (IC50 = 22.4 uM).
价 格：￥电议型 号：T28847产 地：中国大陆
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T28773SI-2；化合物SI-2SI2|||EPH 116|||EPH116|||EPH-116；SI2|||EPH 116|||EPH116|||EPH-116
SI-2 is an inhibitor (SMI) of steroid receptor coactivator-3 (SRC-3 or AIB1). SI-2 can selectively reduce the transcriptional activities and the protein concentrations of SRC-3 in cells, and selectively induce breast cancer cell death with IC50 values in the low nanomolar range (3-20 nM), but not affect normal cell viability.
价 格：￥电议型 号：T28773产 地：中国大陆
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T28762Setrobuvir；化合物SetrobuvirRO-5466731|||ANA-598|||RG7790|||ANA598|||RG-7790；RO-5466731|||ANA-598|||RG77
Setrobuvir (ANA-598) is an orally active non-nucleoside HCV NS5B polymerase inhibitor with inhibitory effects on de novo RNA synthesis and primer extension with IC50s between 4 and 5 nM. setrobuvir shows good binding affinity for SARS-CoV-2 RdRp and induces inhibition of RdRp.
价 格：￥电议型 号：T28762产 地：中国大陆
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T28739SDZ-285604；化合物 T28739SDZ285604|||VNF|||SDZ 285604；SDZ285604|||VNF|||SDZ 285604
SDZ-285604 is a novel sterol 14a-demethylases (CYP51) inhibitor.
价 格：￥电议型 号：T28739产 地：中国大陆
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T28738SDZ-216525；化合物 T28738SDZ 216525|||SDZ216525；SDZ 216525|||SDZ216525
SDZ-216525, a 5-HT1A receptor antagonist, inhibits the tracheal contractions induced both by NKA (10 nM-3 microM) and 5-HT (10 nM-10 microM) (n=4-10).
价 格：￥电议型 号：T28738产 地：中国大陆
