卡比托辛卡贝缩宫素CAS: 37025-55-1原料供应仅供出口

更新时间：2025-01-18 08:00:00

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详细介绍

中文名	卡比托辛
英文名	Carbetocin
别名	卡比托辛卡贝缩宫素醋酸卡贝缩宫素卡贝缩宫素三氟醋酸盐醋酸卡贝缩宫素,卡比托辛卡贝缩宫素-多肽原料委托生产卡贝缩宫素-多肽制剂一致性评价醋酸卡贝缩宫素 37025-55-1
英文别名	Carbetocin CARBETOCIN (BUTYRYL1,TYR(ME)2)-OXYTOCIN CARBETOCIN TRIFLUOROACETATE SALT (2-O-METHYLTYROSINE)-DE-AMINO-1-CARBAOXYTOCIN (BUTYRYL1,TYR(ME)2)-OXYTOCIN TRIFLUOROACETATE SALT (Butyryl1,Tyr(me)2)-1-Carbaoxytocin trifluoroacetate salt (BUTYRYL1,TYR(ME)2)-1-CARBAOXYTOCIN TRIFLUOROACETATE SALT BUTYRYL-TYR(ME)-ILE-GLN-ASN-CYS-PRO-LEU-GLY-NH2 TRIFLUOROACETATE SALT BUTYRYL-TYR(ME)-ILE-GLN-ASN-CYS-PRO-LEU-GLY-NH2, (SULFIDE BOND BETWEEN BUTYRYL-4-YL AND CYS) 1-{[(3R,6S,9S,12S,15S)-6-(2-Amino-2-oxoethyl)-9-(3-amino-3-oxopropyl)-12-[(2S)-butan-2-yl]-15-(4-hydroxybenzyl)-16-methyl-5,8,11,14,17-pentaoxo-1-thia-4,7,10,13,16-pentaazacycloicosan-3-yl]carbonyl}-L-prolyl-L-leucylglycinamide glycinamide, 1-[[(3R,6S,9S,12S,15S)-6-(2-amino-2-oxoethyl)-9-(3-amino-3-oxopropyl)-15-[(4-hydroxyphenyl)methyl]-16-methyl-12-[(1S)-1-methylpropyl]-5,8,11,14,17-pentaoxo-1-thia-4,7,10,13,16-pentaazacycloeicos-3-yl]carbonyl]-L-prolyl-L-leucyl-
CAS	37025-55-1
EINECS	253-312-6
化学式	C45H69N11O12S
分子量	988.17
InChI	InChI=1/C45H69N11O12S/c1-6-25(4)38-44(67)50-28(15-16-34(46)58)40(63)51-30(21-35(47)59)41(64)53-31(23-69-18-8-10-37(61)55(5)33(43(66)54-38)20-26-11-13-27(57)14-12-26)45(68)56-17-7-9-32(56)42(65)52-29(19-24(2)3)39(62)49-22-36(48)60/h11-14,24-25,28-33,38,57H,6-10,15-23H2,1-5H3,(H2,46,58)(H2,47,59)(H2,48,60)(H,49,62)(H,50,67)(H,51,63)(H,52,65)(H,53,64)(H,54,66)/t25-,28-,29-,30-,31-,32-,33-,38-/m0/s1
密度	1.218±0.06 g/cm3(Predicted)
熔点	140 - 160°C
沸点	1477.9±65.0 °C(Predicted)
比旋光度	D -69.0° (c = 0.25 in 1M acetic acid)
闪点	846.7°C
蒸汽压	0mmHg at 25°C
溶解度	DMSO (Slightly), Methanol (Slightly)
折射率	1.541
酸度系数	13.07±0.70(Predicted)
存储条件	-15°C
稳定性	Hygroscopic
外观	powder
颜色	white to beige
体外研究	Carbetocin is an agonist with about 10-fold lower affinity for the oxytocin receptor but with significantly higher stability and a longer duration of action. Carbetocin has higher affinity to the chimeric E1 receptor and especially to each of the combinations of E1 with the other extracellular domains, i.e. chimeric receptors E13 (K i =13 nM), E123 (K i =56 nM), and E1234 (K i =37 nM).