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T11623IDO/TDO-IN-1；化合物 T11623IDO/TDO-IN-1
IDO/TDO-IN-1 is an orally active dual indoleamine-2,3-dioxygenase (IDO) and tryptophan 2,3-dioxygenase (TDO) inhibitor (IC50s: 9.7 and 47 nM).
价 格：￥电议型 号：T11623产 地：中国大陆
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T11622IDO-IN-9；化合物 T11622IDO-IN-9
IDO-IN-9 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.011 μM (Kinase) and 0.0018 μM (Hela Cell).
价 格：￥电议型 号：T11622产 地：中国大陆
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T11621IDO-IN-8；化合物 T11621NLG-1487；NLG-1487
IDO-IN-8 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM).
价 格：￥电议型 号：T11621产 地：中国大陆
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T11620IDO-IN-6；化合物 T11620NLG-1486；NLG-1486
IDO-IN-6 is an indoleamine 2,3-dioxygenase (IDO) inhibitor.
价 格：￥电议型 号：T11620产 地：中国大陆
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T1162Acipimox；阿昔莫司Olbemox|||K-9321；Olbemox|||K-9321|||阿西莫司|||阿昔莫司
Acipimox (K-9321) is a niacin derivative and nicotinic acid analog with activity as a hypolipidemic agent. Acipimox has special application for the treatment of hyperlipidemia in non-insulin-dependent diabetic patients.
价 格：￥电议型 号：T1162产 地：中国大陆
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T11606ICA-105665；化合物 T11606PF-04895162；PF-04895162
ICA-105665 (PF-04895162) is a potent and orally active neuronal Kv7.2/7.3 and Kv7.3/7.5 potassium channels opener. ICA-105665 had low cytotoxic potential in human hepatocytes but inhibited liver mitochondrial function and bile salt export protein (BSEP) transport (IC50 of 311 μM). ICA-105665 can penetrate the central nervous system (CNS) and has antiseizure effects[1][2][3][4].
价 格：￥电议型 号：T11606产 地：中国大陆
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T11562HIF-2α-IN-3；HIF-2α 抑制剂 3HIF-2α-IN-3
HIF-2α-IN-3 is a HIF-2α alteration inhibitor with anti-tumor properties and may be used in the study of cardiovascular disease.
价 格：￥电议型 号：T11562产 地：中国大陆
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T1152Albendazole；阿苯达唑SKF-62979；SKF-62979|||阿苯达唑
Albendazole (SKF-62979) 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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T11508Camicinal；化合物 T11508GSK962040；GSK962040
Camicinal is a selective motilin receptor agonist (pEC50: 7.9).
价 格：￥电议型 号：T11508产 地：中国大陆
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T11472LMolibresib besylate化合物 T11472LI-BET 762 besylate|||GSK 525762C
Molibresib besylate is an inhibitor of BET bromodomain (IC50: 32.5-42.5 nM).
价 格：￥电议型 号：T11472L产 地：中国大陆
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T11469GSK-3484862；化合物GSK-3484862GSK-3484862
Gsk-3484862 is a non covalent inhibitor of DNA methyltransferase DNMT1 with anticancer activity. Gsk-3484862 mediates the global demethylation of mouse embryonic stem cells.
价 格：￥电议型 号：T11469产 地：中国大陆
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T11465Lenacapavir；化合物LenacapavirGS-6207；GS-6207
Lenacapavir (GS-6207) is a potent capsid-targeting inhibitor of HIV replication. Lenacapavir shows anti-HIV activity with an EC50 of 100 pM in MT-4 cells.
价 格：￥电议型 号：T11465产 地：中国大陆
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T11462GPR84 antagonist 8；化合物 T11462GPR84 antagonist 8
GPR84 antagonist 8 is a selective GPR84 antagonist.
价 格：￥电议型 号：T11462产 地：中国大陆
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T11446GNF362；化合物 T11446GNF362
GNF362 is a selective and orally bioavailable inhibitor of inositol trisphosphate 3’ kinase B (Itpkb; IC50: 9 nM). GNF362 also inhibits Itpka and Itpkc (IC50s: 20 nM and 19 nM).
价 格：￥电议型 号：T11446产 地：中国大陆
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T11444GNF-6231；化合物GNF-6231GNF-6231
GNF-6231 is a potent, selective, and orally bioavailable Porcupine inhibitor that blocks Wnt signaling.
价 格：￥电议型 号：T11444产 地：中国大陆
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T11362gamma-Secretase Modulators；化合物 T11362γ-Secretase Modulators|||Amyloid-β production inhibitor；γ-Secre
gamma-Secretase Modulators serves as a useful treatment for Alzheimer´s disease by inhibiting the production of Amyloid-β. Specifically, it acts as a gamma-Secretase Modulators with an IC50 value.
价 格：￥电议型 号：T11362产 地：中国大陆
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T11306Fluvastatin D6 sodium；化合物 T11306XU 62-320 (D6)；XU 62-320 (D6)
Fluvastatin sodium is a first fully synthetic, competitive HMG-CoA reductase inhibitor with an IC50 of 8 nM.Fluvastatin D6 sodium is deuterium labeled Fluvastatin sodium.
价 格：￥电议型 号：T11306产 地：中国大陆
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T11262Falintolol, (Z)-；化合物 T11262Falintolol, (Z)-
Falintolol, (Z)-, is a novel β-adrenergic antagonist compound distinguished by the inclusion of an oxime moiety.
价 格：￥电议型 号：T11262产 地：中国大陆
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T11162EGFR-IN-8；化合物EGFR-IN-8EGFR-IN-8
EGFR-IN-8, a dual inhibitor targeting both EGFR and c-Met, shows potential as a promising candidate for further development in treating EGFR TKI-resistant NSCLC.
价 格：￥电议型 号：T11162产 地：中国大陆
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T11095DREADD agonist 21 dihydrochloride；化合物 T11095DREADD agonist 21 dihydrochloride (56296-18-5 free base)
DREADD agonist 21 dihydrochloride is a potent human muscarinic acetylcholine M3 receptors ( hM3Dq ) agonist with EC 50 of 1.7 nM [1].
价 格：￥电议型 号：T11095产 地：中国大陆
