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T11859LLitronesib；化合物 T11859LKF-89617|||LY-2523355；KF-89617|||LY-2523355
Litronesib is a selective inhibitor of mitosis-specific kinesin Eg5. It also has antitumor activity.
价 格：￥电议型 号：T11859L产 地：中国大陆
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T11859Litronesib Racemate化合物 T11859LY-2523355 Racemate|||KF-89617 Racemate
Litronesib is a selective, allosteric inhibitor of kinesin Eg5.Litronesib (Racemate) is the racemate of litronesib.
价 格：￥电议型 号：T11859产 地：中国大陆
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T1182LLevocarnitine propionate；化合物 T1182LL-Propionylcarnitine|||ST261|||ST 261|||Propionyl-L-carnitine|||S
Propionylcarnitine is present in high abundance in the urine of patients with Methylmalonyl-CoA mutase (MUT) deficiency.
价 格：￥电议型 号：T1182L产 地：中国大陆
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T11823LB-60-OF61；化合物 LB-60-OF61LB-60-OF61
LB-60-OF61 is a NAMPT inhibitor, a NAMPT inhibitor that displays antiproliferative activity against MYC oncogene-dependent cancer cell lines.
价 格：￥电议型 号：T11823产 地：中国大陆
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T11761Tarlox-TKI；化合物 Tarlox-TKIKinase inhibitor-1；Kinase inhibitor-1
Tarlox-TKI (Kinase inhibitor-1) is a pan-ErbB inhibitor, the active ingredient of Tarloxotinib, with antitumor activity.Tarlox-TKI inhibits NRG1 and suppresses HER2 mutants.
价 格：￥电议型 号：T11761产 地：中国大陆
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T11712Jasplakinolide；肌动蛋白多聚化肽Jaspamide|||NSC-613009；Jaspamide|||NSC-613009
Jasplakinolide(Jaspamide), a naturally occurring cyclic peptide from marine sponges, is a potent inducer of actin polymerization.Jasplakinolide exhibits antifungal and antitumor activity and stabilizes pre-existing actin filaments. Jasplakinolide competitively binds to F-actin with the ghost pen cyclic peptide and has a Kd value of 15 nM for F-actin.
价 格：￥电议型 号：T11712产 地：中国大陆
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T11661INT-767；化合物 INT-767INT-767
INT-767 is a potent farnesoid X receptor (FXR)/TGR5 dual agonist that prevents NASH and promotes visceral adipose brown lipogenesis and mitochondrial function for the study of non-alcoholic steatohepatitis.
价 格：￥电议型 号：T11661产 地：中国大陆
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T11619IDO-IN-5；化合物 T11619NLG-1489；NLG-1489
IDO-IN-5 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM).
价 格：￥电议型 号：T11619产 地：中国大陆
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T11618IDO-IN-4；化合物 T11618IDO-IN-4
IDO-IN-4 is an indoleamine 2,3-dioxygenase 1 (IDO-1) inhibitor.
价 格：￥电议型 号：T11618产 地：中国大陆
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T11617IDO-IN-3；化合物 T11617IDO-IN-3
IDO-IN-3 is a potent indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 290 nM).
价 格：￥电议型 号：T11617产 地：中国大陆
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T11616IDO-IN-13；化合物IDO-IN-13GS-4361；GS-4361
IDO-IN-13 (GS-4361) is a potent indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor (EC50: 17 nM).
价 格：￥电议型 号：T11616产 地：中国大陆
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T11615IDO-IN-12；化合物IDO-IN-12IDO-IN-12
IDO-IN-12 is an inhibitor of indoleamine 2,3-dioxygenase (IDO).
价 格：￥电议型 号：T11615产 地：中国大陆
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T11614IDO-IN-11；化合物 T11614IDO-IN-11
IDO-IN-11 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.18 μM (Kinase) and 0.014 μM (Hela Cell).
价 格：￥电议型 号：T11614产 地：中国大陆
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T11613IDH1 Inhibitor 1；化合物 T11613IDH1 Inhibitor 1
IDH1 Inhibitor 1 is an orally bioavailable, brain-penetrant, and selective mutant IDH1 inhibitor (IC50s: 0.021 μM, 0.045 μM, and 2.52 μM for IDH1R132H, IDH1R132C, and IDH1WT).
价 格：￥电议型 号：T11613产 地：中国大陆
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T11612IDH1 Inhibitor 3；化合物 T11612IDH1 Inhibitor 3
IDH1 Inhibitor 3 is a mutant isocitric dehydrogenase 1 (IDH1) inhibitor (IC50: 45 nM for IDH1R132H).
价 格：￥电议型 号：T11612产 地：中国大陆
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T11611IDH1 Inhibitor 2；化合物 T11611IDH1 Inhibitor 2
IDH1 Inhibitor 2 (compound 13) is a potent IDH1 inhibitor via direct covalent modification of His315 (IC50: 110 nM).
价 格：￥电议型 号：T11611产 地：中国大陆
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T11610Idelalisib D5；化合物 T11610CAL-101 D5|||GS-1101 D5；CAL-101 D5|||GS-1101 D5
Idelalisib D5, a version of Idelalisib marked with deuterium, is an orally bioavailable and highly selective inhibitor of p110δ.
价 格：￥电议型 号：T11610产 地：中国大陆
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T1161Prothionamide；丙硫异烟胺1321-TH|||Protionamide；1321-TH|||Protionamide|||丙硫异烟胺
Prothionamide (1321-TH)is a thioamide derivative with antitubercular activity.
价 格：￥电议型 号：T1161产 地：中国大陆
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T1158Phenoxybenzamine hydrochloride；盐酸酚苄明NCI-c01661|||NSC 37448|||Phenoxybenzamine HCl；苯氧苯札明|||NCI-c01661
Phenoxybenzamine hydrochloride (NCI-c01661) is the hydrochloride salt form of phenoxybenzamine, a synthetic, dibenzamine alpha-adrenergic antagonist with antihypertensive and vasodilatory properties. Phenoxybenzamine non-selectively and irreversibly blocks the postsynaptic alpha-adrenergic receptor in smooth muscle, thereby preventing vasoconstriction, relieving vasospasms, and decreasing peripheral resistance. Reflex tachycardia may occur and may be enhanced by blockade of alpha-2 receptors whi
价 格：￥电议型 号：T1158产 地：中国大陆
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T11561HIF-2α-IN-2；化合物HIF-2α-IN-2HIF-2α-IN-2
HIF-2α-IN-2 is a hypoxia-inducible factor (HIF-2α) inhibitor (IC50: 16 nM in scintillation proximity assay).
价 格：￥电议型 号：T11561产 地：中国大陆
