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6′-GNTI 二(三氟乙酸) 盐_分子结构_CAS_35080-00-3(anhydrous))
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6′-GNTI 二(三氟乙酸) 盐

产品号 G0921 公司名称 Sigma Aldrich
CAS号 35080-00-3(anhydrous) 公司网站 http://www.sigmaaldrich.com
分子式 C31H35F6N5O9 电 话 1-800-521-8956
分子量 735.6281192 传 真
纯 度 ≥97.5% (HPLC) 电子邮件
保 存 desiccated Chembase数据库ID: 153148

产品价格信息

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产品别名

标题
6′-Guanidinonaltrindole ditrifluoroacetate dihydrate
IUPAC标准名
1-[(1S,2S,13R,21R)-22-(cyclopropylmethyl)-2,16-dihydroxy-14-oxa-11,22-diazaheptacyclo[13.9.1.01,13.02,21.04,12.05,10.019,25]pentacosa-4(12),5,7,9,15(25),16,18-heptaen-8-yl]guanidine bis(trifluoroacetic acid) dihydrate
IUPAC传统名
1-[(1S,2S,13R,21R)-22-(cyclopropylmethyl)-2,16-dihydroxy-14-oxa-11,22-diazaheptacyclo[13.9.1.01,13.02,21.04,12.05,10.019,25]pentacosa-4(12),5,7,9,15(25),16,18-heptaen-8-yl]guanidine bis(trifluoroacetic acid) dihydrate
别名
6′-GNTI
[(4bS,8R,8aS,14bR)-7-(Cyclopropylmethyl)-5,6,7,8,8a,9,14,14b-octahydro-1,8a-dihydroxy-4,8-methanobenzofuro[2,3-a]pyrido[4,3-b]carbazol-12-yl]-guanidine ditrifluoroacetate dihydrate
: [(4bS,8R,8aS,14bR)-7-(cyclopropylmethyl)-5,6,7,8,8a,9,14,14b-octahydro-1,8a-dihydroxy-4,8-methanobenzofuro[2,3-a]pyrido[4,3-b]carbazol-12-yl]-guanidine ditrifluoroacetate dihydrate

产品登记号

MDL号 MFCD09752601
CAS号 35080-00-3(anhydrous)

产品性质

Empirical Formula (Hill Notation) C27H29N5O3 · 2CF3CO2H · 2H2O
纯度 ≥97.5% (HPLC)
外观 pink to tan solid
溶解度 H2O: >20 mg/mL
MSDS下载 下载链接
个人保护装置 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
保存条件 desiccated
保存条件 under inert gas
保存温度 -20°C
德国WGK号 3

产品详细信息

详细说明 (English)
Caution
Air-sensitive
Biochem/physiol Actions
6′-GNTI is a selective agonist of κ/δ opioid receptor heterodimers in the spinal cord and has the unique property of selectively activating only opioid receptor heterodimers and not homomers. 6′-GNT functions as an analgesic demonstrating that opioid receptor heterodimers are functionally relevant in vivo.
详细说明 (简体中文)
Caution
Air-sensitive
Biochem/physiol Actions
6′-GNTI is a selective agonist of κ/δ opioid receptor heterodimers in the spinal cord and has the unique property of selectively activating only opioid receptor heterodimers and not homomers. 6′-GNT functions as an analgesic demonstrating that opioid receptor heterodimers are functionally relevant in vivo.

参考文献