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T13915LPROTAC BRD9-binding moiety 1 hydrochloride；化合物 T13915LPROTAC BRD9-binding moiety 1 hydrochloride (20
PROTAC BRD9-binding moiety 1 hydrochloride binds to BRD9, and used for inhibiting BRD9 activity, based on PROTAC.
价 格：￥电议型 号：T13915L产 地：中国大陆
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T13915PROTAC BRD9-binding moiety 1；化合物 T13915PROTAC BRD9-binding moiety 1
PROTAC BRD9-binding moiety 1 that binds to BRD9, and used for inhibiting BRD9 activity, based on PROTAC.
价 格：￥电议型 号：T13915产 地：中国大陆
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T13889SLLN-15；化合物 T13889SLLN-15
SLLN-15 is an oral active, selective and potent enhancer of autophagy. SLLN-15 activates cytostatic macroautophagy/autophagy in triple-negative breast cancer (TNBC) [1].
价 格：￥电议型 号：T13889产 地：中国大陆
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T13715LGSK9311；化合物 T13715LGSK9311
GSK9311 inhibits BRPF bromodomain (pIC50: 6.0 and 4.3 for BRPF1 and BRPF2, respectively). GSK9311 is a less active analog of GSK6853. It can be used as a negative control.
价 格：￥电议型 号：T13715L产 地：中国大陆
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T13715GSK9311 hydrochloride；化合物 T13715GSK9311 hydrochloride
GSK9311 hydrochloride, a less active analog of GSK6853, can be used as a negative control. GSK9311 hydrochloride inhibits BRPF bromodomain (pIC50s: 6.0 and 4.3 for BRPF1 and BRPF2).
价 格：￥电议型 号：T13715产 地：中国大陆
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T13711Glyhexamide；化合物 T13711Subose|||SQ 15860|||Serbose；Subose|||SQ 15860|||Serbose
Glyhexamide is an effective hypoglycemic compound.
价 格：￥电议型 号：T13711产 地：中国大陆
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T13696FN-1501-propionic acid；化合物 T13696FN-1501-propionic acid
FN-1501-propionic acid, a CDK2/9 ligand, in conjunction with a CRBN ligand, has been utilized in the design of a PROTAC CDK2/9 degrader.
价 格：￥电议型 号：T13696产 地：中国大陆
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T13658DMEA-PNU-159682；化合物 T13658DMEA-PNU-159682
DMEA-PNU-159682 (molecule D12) is an ADC cytotoxin molecule, including neomycin (MMDX) metabolites from liver microsomes and effective ADC cytotoxin PNU-159682.
价 格：￥电议型 号：T13658产 地：中国大陆
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T13615Cinperene；桂哌林R5046；桂哌林|||R5046
Cinperene is an atropine-like compound that can block pilocarpine-induced salivation and lacrimation.
价 格：￥电议型 号：T13615产 地：中国大陆
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T13607CGP 65015；化合物 T13607CGP 65015
CGP 65015 is an oral iron chelator and can mobilize iron deposits.
价 格：￥电议型 号：T13607产 地：中国大陆
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T135155-Methoxytryptophol；5-甲氧基色醇2-(5-Methoxy-1H-indol-3-yl)ethanol|||Methoxytryptophol；2-(5-Methoxy-1H-in
5-Methoxytryptophol (2-(5-Methoxy-1H-indol-3-yl)ethanol) is a pineal indoleamine derived from serotonin shown to be biologically active in a number of species.
价 格：￥电议型 号：T13515产 地：中国大陆
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T13467(±)-Enitociclib；化合物(±)-BAY-1251152(±)-BAY-1251152；(±)-BAY-1251152
(±)-Enitociclib ((±)-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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T13455(S)-Tedizolid；(S)-特地唑胺(S)-TR 700|||(S)-DA 7157；(S)-TR 700|||(S)-特地唑胺|||(S)-DA 7157
(S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens.
价 格：￥电议型 号：T13455产 地：中国大陆
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T13424(1R,2S)-VU0155041；化合物(1R,2S)-VU0155041(1R,2S)-VU0155041
(1R,2S)-VU0155041 is the cis regioisomer of VU0155041 and a partial agonist of mGluR4.
价 格：￥电议型 号：T13424产 地：中国大陆
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T13390ZD 7155 hydrochloride；ZD 7155盐酸盐ZD 7155 hydrochloride
ZD 7155 hydrochloride is an angiotensin II receptor type 1 (AT1 receptor) antagonist.
价 格：￥电议型 号：T13390产 地：中国大陆
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T13332(Rac)-WAY-161503；化合物(Rac)-WAY-161503(Rac)-WAY-161503
(Rac)-WAY-161503 is a selective and high-affinity agonist of the 5-HT2C receptor (Ki: 4 nM; EC50: 12 nM), with anti-obesity and antidepressant effects.
价 格：￥电议型 号：T13332产 地：中国大陆
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T13315VU 6008667化合物 T13315VU 6008667
VU 6008667 is a selective negative allosteric M5 NAM modulator (IC50s: 1.2 μM and 1.6 μM for human M5 and rat M5, respectively).
价 格：￥电议型 号：T13315产 地：中国大陆
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T13310VP3.15；化合物 T13310VP3.15
VP3.15 is an orally bioavailable and CNS-penetrant dual inhibitor of phosphodiesterase (PDE)7- GSK3 (IC50s: 1.59 μM and 0.88 μM for PDE7 and GSK-3).
价 格：￥电议型 号：T13310产 地：中国大陆
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T13294Veledimex (S enantiomer)；化合物 T13294RG-115932 S enantiome|||INXN-1001 S enantiome；RG-115932 S enantio
Veledimex S enantiomer is the S enantiomer of veledimex. Veledimex is an oral activator ligand for a proprietary gene therapy promoter system and CYP3A4/5 inhibitor.
价 格：￥电议型 号：T13294产 地：中国大陆
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T13293LVeledimex；化合物 T13293LRG-115932|||INXN-1001；RG-115932|||INXN-1001
Veledimex is an oral activator ligand for a proprietary gene therapy promoter system. It is also a moderate inhibitor of and substrate for CYP3A4/5.
价 格：￥电议型 号：T13293L产 地：中国大陆
