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T1163Betamethasone valerate；倍他米松戊酸酯Betnovate|||Betaderm|||Betamethasone 17-valerate|||Luxiq；Betnovate|||倍
Betamethasone valerate (Luxiq) is a synthetic glucocorticoid with metabolic, immunosuppressive and anti-inflammatory actions.
价 格：￥电议型 号：T1163产 地：中国大陆
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T11629Ifenprodil glucuronide；化合物 T11629Ifenprodil glucuronide
Ifenprodil glucuronide, a derivative of Ifenprodil, is a vasodilator and an inhibitor of platelet aggregation. In contrast to Ifenprodil, Ifenprodil glucuronide does not affect platelet aggregation nor arterial contraction.
价 格：￥电议型 号：T11629产 地：中国大陆
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T11628IACS-8968 S-enantiomer；化合物 T11628IDO/TDO Inhibitor (S-enantiomer)；IDO/TDO Inhibitor (S-enantiomer)
IACS-8968 S-enantiomer is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
价 格：￥电议型 号：T11628产 地：中国大陆
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T11627IACS-8968 R-enantiomer；化合物 T11627IDO/TDO Inhibitor (R-enantiomer)；IDO/TDO Inhibitor (R-enantiomer)
IACS-8968 R-enantiomer is the R-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
价 格：￥电议型 号：T11627产 地：中国大陆
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T11626IACS-8968；化合物 T11626IDO/TDO Inhibitor；IDO/TDO Inhibitor
IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
价 格：￥电议型 号：T11626产 地：中国大陆
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T11625IDO1 and HDAC1 Inhibitor；化合物 T11625IDO1 and HDAC1 Inhibitor
IDO1 and HDAC1 Inhibitor is a dual IDO1 and HDAC1 inhibitor (IC50s: 69.0 nM and 66.5 nM).
价 格：￥电议型 号：T11625产 地：中国大陆
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T11624IDO1-IN-2；化合物 T11624IDO1-IN-2
IDO1-IN-2 is a potent and selective IDO1 inhibitor with IC50s of 81 nM, 59 nM (mouse), and 28 nM (rat), respectively. It has anti-cancer activity.
价 格：￥电议型 号：T11624产 地：中国大陆
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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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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
