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T101745-R-Rivaroxaban；5-R-利伐沙班5-R-Rivaroxaban
5-R-Rivaroxaban is (R)-enantiomer of Rivaroxaban. Rivaroxaban (BAY 59-7939) is a highly potent and selective, direct Factor Xa (FXa) inhibitor (IC50 0.7 nM; Ki 0.4 nM).
价 格：￥电议型 号：T10174产 地：中国大陆
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T10173MCHR1 antagonist 1；化合物 T10173MCHR1 antagonist 1
MCHR1 antagonist 1 is a selective antagonist of melanin-concentrating hormone-1 (MCH1) receptor (Kb: 1 nM, Ki: 4 nM at human MCH1).
价 格：￥电议型 号：T10173产 地：中国大陆
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T101715-Hydroxypyrazine-2-Carboxylic Acid；化合物 T101715-Hydroxypyrazine-2-Carboxylic Acid
5-Hydroxypyrazine-2-Carboxylic Acid is a metabolite of anti-tuberculosis drug pyrazinamide.
价 格：￥电议型 号：T10171产 地：中国大陆
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T101705-HT7 agonist 1；化合物5-HT7 agonist 14-[4-[(2-chlorophenyl)methyl]-1-piperazinyl]-1H-indole|||4-[4-[(2-
5-HT7 agonist 1 (4-[4-[(2-chlorophenyl)methyl]piperazin-1-yl]-1H-indole) is a selective agonist of 5-HT7 (IC50 = 222.93 nM). 5-HT7 agonist 1 can be used in studies about CNS disorders.
价 格：￥电议型 号：T10170产 地：中国大陆
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T1017Fluorothyl；氟替尔Fluoroethyl|||Flurothyl|||Bis(2,2,2-trifluoroethyl) ether；Fluoroethyl|||Flurothyl|||Bi
Fluorothyl (Bis(2,2,2-trifluoroethyl) ether) is a convulsant used in experimental animals.
价 格：￥电议型 号：T1017产 地：中国大陆
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T101675-Dehydroepisterol；化合物 T101675-Dehydroepisterol
5-Dehydroepisterol is an episterol derivative with anti-fungal activities. It can be formed by C-5 sterol desaturase and converted into 24-methylenecholesterol by 7-dehydrocholesterol reductase.
价 格：￥电议型 号：T10167产 地：中国大陆
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T1015948740 RP；化合物48740 RPRP-48740|||RP-55778|||RP 55779|||RP 55778；RP-48740|||RP-55778|||RP 55779|||RP 55
48740 RP (RP 55779) is an antagonist of platelet-activating factor.
价 格：￥电议型 号：T10159产 地：中国大陆
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T10157Regorafénib N-oxyde (M2)瑞戈非尼杂质 13瑞戈非尼杂质 13
Regorafénib N-oxyde M2 is an active metabolite of Regorafenib. Regorafenib is a multi-target inhibitor for VEGFR1/2/3, PDGFRβ, RET, Kit, and Raf-1 (IC50s: 13/4.2/46, 1.5, 22, 7, and 2.5 nM).
价 格：￥电议型 号：T10157产 地：中国大陆
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T101494-Hydroxypropranolol-d7 hydrochloride；化合物 T10149(±)-4-hydroxy Propranolol D7 hydrochloride|||4-Hydro
4-Hydroxypropranolol D7 hydrochloride is deuterium-labeled 4-Hydroxypropranolol hydrochloride. 4-Hydroxypropranolol hydrochloride is an active metabolite of Propranolol, with a potency comparable to Propranolol. It inhibits β1- and β2-adrenergic receptors (pA2s: 8.24 and 8.26).
价 格：￥电议型 号：T10149产 地：中国大陆
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T101374-Bromo A23187；化合物 T101374-?Bromo A23187；4-?Bromo A23187
4-Bromo A23187 is a halogenated analog of the calcium ionophore A-23187. 4-Bromo A23187 is a calcium modulator and induces apoptosis in different cells.
价 格：￥电议型 号：T10137产 地：中国大陆
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T101344,7,10,13,16-Docosapentaenoic acid；化合物 T101344,7,10,13,16-Docosapentaenoic acid
4,7,10,13,16-Docosapentaenoic acid is an endogenous metabolite.
价 格：￥电议型 号：T10134产 地：中国大陆
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T10127(3R,5S)-Atorvastatin sodium；化合物 T10127(3R,5S)-Atorvastatin sodium
(3R,5S)-Atorvastatin sodium is an impurity of Atorvastatin. Atorvastatin is an HMG-CoA reductase inhibitor and has the ability to effectively decrease blood lipids.
价 格：￥电议型 号：T10127产 地：中国大陆
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T101193-O-Methyltolcapone；化合物 T10119Ro 40-7591；Ro 40-7591
3-O-Methyltolcapone (Ro 40-7591) is a metabolite of Tolcapone which is a potent COMT inhibitor. Tolcapone crosses the blood-brain barrier and can be used for treatment of Parkinson´s disease.
价 格：￥电议型 号：T10119产 地：中国大陆
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T101183-O-Methyltolcapone D7；化合物 T10118Ro 40-7591 D7；Ro 40-7591 D7
3-O-Methyltolcapone D7 (Ro 40-7591 D7) is a deuterium labeled 3-O-Methyltolcapone. 3-O-Methyltolcapone (Ro 40-7591) is a metabolite of Tolcapone which is a potent COMT inhibitor. Tolcapone crosses the blood-brain barrier and can be used for treatment of Parkinson´s disease.
价 格：￥电议型 号：T10118产 地：中国大陆
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T101073-Bromo-7-nitroindazole；3-溴-7-铌溴呋喃酯3-Bromo-7-nitroindazole
3-Bromo-7-nitroindazole is a specific neuronal nitric oxide synthase (nNOS) inhibitor. It affects the intercellular messenger NO synthesis throughout the brain and body.
价 格：￥电议型 号：T10107产 地：中国大陆
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T101043,4-Dihydroxybenzylamine hydrobromide；3,4-二羟基苄胺·氢溴酸NSC 263475 hydrobromide；NSC 263475 hydrobromide||
3,4-Dihydroxybenzylamine hydrobromide (NSC-263475 hydrobromide) inhibits DNA polymerase activity in melanoma cells and displays growth inhibitory activity in melanoma cell lines with varying degrees of tyrosinase activity.
价 格：￥电议型 号：T10104产 地：中国大陆
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T10097(2S,3S)-E1R；化合物 T10097(2S,3S)-E1R
(2S,3S)-E1R (Compound 2d) is an enantiomer of E1R. (2R,3R)-E1R is a sigma-1 receptor positive allosteric modulator for the treatment of cognition/memory disorders.
价 格：￥电议型 号：T10097产 地：中国大陆
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T10096L2(2S,3R)-Voruciclib hydrochloride；化合物 T10096L2(2S,3R)-Voruciclib hydrochloride (1253731-24-6 free bas
(2S,3R)-Voruciclib hydrochloride is the (2S,3R)-enantiomer of Voruciclib. It is an orally active CDK inhibitor.
价 格：￥电议型 号：T10096L2产 地：中国大陆
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T1008724-Norursodeoxycholic acid；化合物24-Norursodeoxycholic acidnor-UDCA；nor-UDCA
24-Norursodeoxycholic acid (nor-UDCA) is a side chain-shortened C23 homolog of UDCA.It has shown potent anti-inflammatory, anti-cholestatic, and anti-fibrotic properties.It is a Ursodeoxycholic Acid derivative. It is superior to Ursodeoxycholic acid in the treatment of sclerosing cholangitis in Mdr2 (Abcb4) knockout mice
价 格：￥电议型 号：T10087产 地：中国大陆
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T10080PF-592379；化合物 T10080PF-592379
PF-592379 is a potent agonist of dopamine D3 receptor (EC50: 21 nM).
价 格：￥电议型 号：T10080产 地：中国大陆
