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T3618GSK-2881078GSK2881078；GSK 2881078
GSK2881078 is a selective androgen receptor modulator (SARM) that is being evaluated for effects on muscle growth and strength in subjects with muscle wasting to improve their physical function.
价 格：￥电议型 号：T3618产 地：中国大陆
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T8608LFanetizole mesylate；化合物 T8608LUNII-D3OG7B0G4M|||CP 48810|||Fanetizole mesylate (USAN)|||C1MHW3X；UNII
Fanetizole mesylate is an immunoregulator agent.
价 格：￥电议型 号：T8608L产 地：中国大陆
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T78810BWA-522；化合物 BWA-522BWA-522
BWA-522 is a small molecule, orally available protein-targeting chimera (PROTAC) that potentates the degradation of both full-length androgen receptor (AR-FL) and the AR-V7 splice variant. It specifically antagonizes the N-terminal domain (AR-NTD) of the androgen receptor (Androgen Receptor), prompting apoptosis in prostate cancer (PC) cells. In LNCaP xenograft models, BWA-522 demonstrated tumor growth inhibition (60 mg/kg, po; TGI=76%). The compound effectively reduced levels of AR-V7 and AR-FL
价 格：￥电议型 号：T78810产 地：中国大陆
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T68810MK-0736 hydrochloride；化合物 MK-0736 hydrochlorideMK-0736 hydrochloride
MK-0736 hydrochloride is a potent and selective 11β-HSD-1 inhibitor.
价 格：￥电议型 号：T68810产 地：中国大陆
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T38810BM-1197；BM-1197BM-1197
BM-1197, a highly potent and specific dual inhibitor of Bcl-2 and Bcl-xL, effectively targets these proteins with IC50 values of 3.5 nM and 5.2 nM for Bcl-2 and Bcl-xL, respectively. This compound demonstrates notable antitumor activity in both in vitro and in vivo settings.
价 格：￥电议型 号：T38810产 地：中国大陆
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T38114AL 8810 ethyl amide；AL 8810 ethyl amideAL 8810 ethyl amide
AL 8810 is an 11β-fluoro analog of prostaglandin F2α (PGF2α) which acts as a potent and selective antagonist at the FP receptor. AL 8810 ethyl amide is an analog of AL 8810 in which the C-1 carboxyl group has been modified to an N-ethyl amide. This modification is analogous to the PG N-ethyl amides, as typified by Bimatoprost, that have been introduced as alternative PG ocular hypotensive prodrugs. In contrast to AL 8810 which contracted the cat iris, AL 8810 ethyl amide showed no contraction ac
价 格：￥电议型 号：T38114产 地：中国大陆
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T3618GSK-2881078；化合物GSK2881078GSK2881078|||GSK 2881078；GSK2881078|||GSK 2881078
GSK-2881078 is a selective androgen receptor modulator (SARM) that is being evaluated for effects on muscle growth and strength in subjects with muscle wasting to improve their physical function.
价 格：￥电议型 号：T3618产 地：中国大陆
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T34388Rorifamide；化合物 T3438810-(Methylsulfonyl)decanamide Systematic Name|||Decanamide, 10-(methylsulfonyl)
Rorifamide is crystalline substance isolated from herb Han-Tsai, Rorippa montana (Cruciferae).
价 格：￥电议型 号：T34388产 地：中国大陆
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T28810SM 21；化合物 T28810SM21|||SM-21|||(±)-SM21；SM21|||SM-21|||(±)-SM21
SM 21 is a sigma(2) antagonist.
价 格：￥电议型 号：T28810产 地：中国大陆
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T26842Bms 188107；化合物 T26842Bms188107|||Bms-188107；Bms188107|||Bms-188107
Bms 188107 is a calcium antagonist, it has cardioprotective effects.
价 格：￥电议型 号：T26842产 地：中国大陆
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T21752AL 8810；化合物 T21752AL 8810
AL-8810 is an 11β-fluoro analog of PGF 2α with selective antagonist effects at the PGF 2α receptor (FP receptor) [1].
价 格：￥电议型 号：T21752产 地：中国大陆
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T18810Thalidomide-NH-C6-NH2；化合物 T18810Thalidomide-NH-C6-NH2
Thalidomide-NH-C6-NH2 is a synthetic conjugate compound designed as an E3 ligase ligand-linker. It consists of a Thalidomide-based cereblon ligand linked to a specific linker utilized in PROTAC technology[1].
价 格：￥电议型 号：T18810产 地：中国大陆
