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T11517GV-58；化合物GV-58GV-58
GV-58 is a selective N- and P/Q-type Ca2+ channels agonist (EC50: 7.21/8.81 uM for N-type/P-Q-type Ca2+ channel). The inhibitory of GV-58 is 20-fold fewer for CDK kinases activity.
价 格：￥电议型 号：T11517产 地：中国大陆
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T11516GV-196771A；化合物GV-196771AGV-196771A
GV-196771A A novel NMDA receptor glycine site antagonist with potent antinociceptive activity.
价 格：￥电议型 号：T11516产 地：中国大陆
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T11515Gut restricted-7；化合物Gut restricted-7GR-7；GR-7
Gut restricted-7 (GR-7) (GR-7) is a covalent and orally active pan-bile salt hydrolase (BSH) inhibitor. It decreases gut bacterial BSHs and decreases deconjugated bile acid levels in the feces of mice.
价 格：￥电议型 号：T11515产 地：中国大陆
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T11514Gusperimus trihydrochloride；化合物 T11514NKT-01|||BMS181173|||Spanidin；NKT-01|||BMS181173|||Spanidin
Gusperimus trihydrochloride is a derivative of the antitumor antibiotic spergualin with immunosuppressant activity.
价 格：￥电议型 号：T11514产 地：中国大陆
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T11513Gum arabic；阿拉伯胶Arabic gum；Arabic gum|||阿拉伯胶
Gum Arabic, a branched-chain, complex polysaccharide derived from A. Senegal, exhibits antioxidant properties and offers protection against experimental hepatic, renal, and cardiac toxicities. Additionally, it finds application in immunohistochemistry.
价 格：￥电议型 号：T11513产 地：中国大陆
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T11512Guanoxabenz；化合物 T11512Hydroxyguanabenz；Hydroxyguanabenz
Guanoxabenz is an α2 adrenergic receptor agonist.
价 格：￥电议型 号：T11512产 地：中国大陆
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T11510Guanfu base I；化合物 T11510Acorine；Acorine
Guanfu base I is an active metabolite of Guanfu base A, isolated from Aconitum coreanum. It have a potent anti-arrhythmic effect.
价 格：￥电议型 号：T11510产 地：中国大陆
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T1151Roxithromycin；罗红霉素Roxl-150|||RU-28965；Roxl-150|||罗红霉素|||RU-28965
Roxithromycin (RU-28965) is a semi-synthetic derivative of the macrolide antibiotic erythromycin with antibacterial and anti-malarial activities.
价 格：￥电议型 号：T1151产 地：中国大陆
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T11509Guanfu base H；化合物 T11509Atisinium chloride；Atisinium chloride
Guanfu base H is a diterpenoid alkaloid isolated from Aconitum coreanum. It has antiplasmodial activity against the malarial Plasmodium falciparum strains TM4/8.2 (wild type) and K1CB1 (IC50s: 4 μM and 3.6 μM).
价 格：￥电议型 号：T11509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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T11507Guancydine化合物 T11507Guancidine
Guancydine is an antihypertensive agent.
价 格：￥电议型 号：T11507产 地：中国大陆
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T11506Guaiapate；愈创哌特Mg 5454|||Klamar；Mg 5454|||Klamar
Guaiapate has an antitussive and sedative effect.
价 格：￥电议型 号：T11506产 地：中国大陆
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T11505GSTO1-IN-1；化合物GSTO1-IN-1GSTO1-IN-1
GSTO1-IN-1 is a potent glutathione S-transferase omega 1 inhibitor (GSTO1; IC50: 31 nM).
价 格：￥电议型 号：T11505产 地：中国大陆
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T11504GSTO-IN-2；化合物 T11504GSTO-IN-2
GSTO-IN-2 is a glutathione S-transferase inhibitor (IC50s: 1.4, 16.3, and 3.6 μM for GSTP1-1, GSTM1, and GSTA2).
价 格：￥电议型 号：T11504产 地：中国大陆
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T11503GSK 690 Hydrochloride；化合物 T11503GSK 690 Hydrochloride
GSK 690 (Hydrochloride) is a reversible lysine specific demethylase 1 (LSD1) inhibitor with a Kd value of 9 nM and IC 50 of 37 nM.
价 格：￥电议型 号：T11503产 地：中国大陆
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T11502Epelsiban；化合物 T11502GSK 557296；GSK 557296
Epelsiban is a selective and orally bioavailable oxytocin receptor antagonist (pKi: 9.9 for human oxytocin receptor).
价 格：￥电议型 号：T11502产 地：中国大陆
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T11500LGSK3368715 dihydrochlorideGSK3368715盐酸盐EPZ019997 dihydrochloride|||GSK3368715 2HCl|||EPZ019997 2HCl
GSK3368715 dihydrochloride (EPZ019997 dihydrochloride) is an orally active and potent inhibitor of type I protein arginine methyltransferases (PRMTs) with anticancer and antitumor activity, inhibiting PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8, and can be used to study advanced solid tumors.
价 格：￥电议型 号：T11500L产 地：中国大陆
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T11500GSK3368715；化合物 T11500EPZ019997；EPZ019997
GSK3368715 is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferases (PRMTs) inhibitor (IC50s: 3.1 nM (PRMT1), 48 nM (PRMT3), 1148 nM (PRMT4), 5.7 nM (PRMT6), 1.7 nM (PRMT8)). It has strong anti-cancer activity.
价 格：￥电议型 号：T11500产 地：中国大陆
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T11487LFiboflapon sodium；化合物 T11487LGSK2190915 sodium salt|||AM-803 sodium；GSK2190915 sodium salt|||AM-803
Fiboflapon sodium (GSK2190915) is an orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9 nM in FLAP binding, an IC50 of 76 nM for inhibition of LTB4 in human blood.
价 格：￥电议型 号：T11487L产 地：中国大陆
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T11487Fiboflapon；化合物FiboflaponGSK2190915|||AM-803；GSK2190915|||AM-803
Fiboflapon (GSK2190915) is an orally available and effective 5-lipoxygenase-activating protein (FLAP) inhibitor that binds FLAP with a titer of 2.9 nM and inhibition of LTB4 in human blood with an IC50 of 76 nM.
价 格：￥电议型 号：T11487产 地：中国大陆
