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3-羟甲基-β-咔啉

更新时间:2025-09-18 15:36:33

3-羟甲基-β-咔啉结构式
3-羟甲基-β-咔啉结构式
品牌特惠专场
常用名 3-羟甲基-β-咔啉 英文名 3-HYDROXYMETHYL-BETA-CARBOLINE
CAS号 65474-79-5 分子量 198.22100
密度 1.385 g/cm3 沸点 466ºC at 760 mmHg
分子式 C12H10N2O 熔点 N/A
MSDS 中文版 美版 闪点 235.6ºC

 3-羟甲基-β-咔啉名称

中文名 3-羟甲基-β-咔啉
英文名 9H-pyrido[3,4-b]indol-3-ylmethanol
中文别名 3-羟甲基-Β-咔啉
英文别名 更多

 3-羟甲基-β-咔啉物理化学性质

密度 1.385 g/cm3
沸点 466ºC at 760 mmHg
分子式 C12H10N2O
分子量 198.22100
闪点 235.6ºC
精确质量 198.07900
PSA 48.91000
LogP 2.20840
InChIKey CPBYHTDUBNSBQM-UHFFFAOYSA-N
SMILES OCc1cc2c(cn1)[nH]c1ccccc12
外观性状 黄色固体
折射率 1.795

 3-羟甲基-β-咔啉安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危险品运输编码 NONH for all modes of transport
海关编码 2933990090

 3-羟甲基-β-咔啉海关

海关编码 2933990090
中文概述 2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
申报要素 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 3-羟甲基-β-咔啉文献9

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Do benzodiazepine receptors play a role in sleep regulation? Studies with the benzodiazepine antagonist, 3-hydroxymethyl-beta-carboline (3-HMC).

Prog. Clin. Biol. Res. 90 , 253-61, (1982)

Electrophysiological studies on benzodiazepine antagonists.

Brain Res. 295(2) , 265-74, (1984)

The actions of the benzodiazepine (BDZ) antagonists 3-hydroxymethyl-beta-carboline (3-HMC), Ro 14-7437 and Ro 15-1788 were tested on single cell activity of rat hypothalamic neurons in tissue cultures...

The interaction between benzodiazepine antagonists and barbiturate-induced cerebrovascular and cerebral metabolic depression.

Neuropharmacology 24(10) , 957-63, (1985)

It has been reported that pentobarbital facilities binding to benzodiazepine receptors binding at anesthetic concentrations and that this action may play a role in the anesthetic potency of this barbi...

 3-羟甲基-β-咔啉靶点实验

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实验名称:Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-p1-antagonist
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Stage-Specific Inhibitors of Vaccinia Orthopoxvirus: mCherry Reporter Primar...
来源:NCGC
靶标:67.9K protein [Vaccinia virus]
External Id:Vaccinia-p2mCherry
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:In vitro inhibition of [3H]diazepam binding to rat cerebral cortical membrane benzodi...
来源:ChEMBL
靶标:Gamma-aminobutyric acid receptor subunit alpha-3
External Id:CHEMBL653130
实验名称:Cytotoxicity against human MCF-10A cells assessed as inhibition of cell proliferation...
来源:ChEMBL
靶标:MCF-10A
External Id:CHEMBL4837051
实验名称:Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of c...
来源:ChEMBL
靶标:MDA-MB-231
External Id:CHEMBL4837050
实验名称:qHTS for Stage-Specific Inhibitors of Vaccinia Orthopoxvirus: Venus Reporter Primary ...
来源:NCGC
靶标:67.9K protein [Vaccinia virus]
External Id:Vaccinia-p2Venus
实验名称:Antiproliferative activity against human MCF7 cells assessed as inhibition of cell pr...
来源:ChEMBL
靶标:MCF7
External Id:CHEMBL4837049
实验名称:Cytotoxicity against human A498 cells incubated for 48 hrs by MTT assay
来源:ChEMBL
靶标:A498
External Id:CHEMBL3611212
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 3-羟甲基-β-咔啉英文别名

3-HMC
9H-Pyrido[3,4-b]indole-3-methanol
Prestwick_970
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