伊立替康厂家生产原药喜树碱价格

Irinotecan
97682-44-5

湖南更新日期：2017-10-17

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产品详情:

中文名称：: 伊立替康厂家生产原药喜树碱价格

英文名称：: Irinotecan

CAS号：: 97682-44-5

品牌：: 精品伊立替康

产地：: 伊立替康18689490047

保存条件：: 干燥

纯度规格：: 99

中文名称: 伊立替康

中文同义词: [1,4'-联哌啶]-1'-羧酸(S)-4,11-二乙基-3,4,12,14-四氢-4羟基-3,14-二氧-1H-吡喃并[3',4':6,7]氮茚[1,2-B]喹啉-9-基酯;联哌喜树碱;(S)-4,11-二乙基-3,4,12,14-四氢-4-羟基-3,14-二氧代-1H-吡喃;伊立替康碱;(S)-4,11-二乙基-3,4,12,14-四氢-4-羟基-3,14-二氧代-1H-吡喃并[3',4':6,7]中氮茚并[1,2-B]喹啉-9-基 1,4'-联哌啶-1'-羧酸酯;伊立替康三水盐酸盐;伊立替康(替康类);伊立替康(标准品)

英文名称: Irinotecan

英文同义词: Irinotecan (free Base);Irinotecan(TECANS);1,4'-Bipiperidine-1'-carboxylic acid (S)-4,11-diethyl-3,4,12,14- tetrahydro-4-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl ester;DQ-2805;(4S)-4,11-Diethyl-4-hydroxy-9-[[(4-piperidinopiperidino)carbonyl]oxy]-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14-dione;SN-38-11;(19S)-10,19-diethyl-19-hydroxy-14,18-dioxo-17-oxa-3,13-diazapentacyclo[11.8.0.0^{2,11}.0^{4,9}.0^{15,20}]henicosa-1(21),2,4(9),5,7,10,15(20)-heptaen-7-yl 4-(piperidin-1-yl)piperidine-1-carboxylate;(4S)-4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl-[1,4'-bipiperidine]-1'-carboxylic acid

CAS号: 97682-44-5

分子式: C33H39ClN4O6

分子量: 623.14

EINECS号:

相关类别: TECANS替康类产品(Anti-cancer);Camptothecin series;喜树碱系列;APIs;Natural Anti-cancer Medical Materials and It's Derivatives;API's;动植物类抗肿瘤药物;抗肿瘤药;药物;API;标准品;植物提取物;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Camptosar, Campto;Anti-cancer&immunity;医药中间体;喜树碱的半合成衍生物;Anti cancer;Inhibitors;小分子抑制剂，天然产物;医药原料;医药原料药;DNA损伤

化学性质淡黄色粉末，熔点222~223℃。

盐酸伊立替康(Irinotecan Hydrochloride)：C33H38N4O6?HCl?3H2O。[136572-09-3]。从水得极淡黄色针状结晶或结晶性粉末，熔点256.5℃。[α]D20+67.7°(C=1，水)。UV吸收(乙醇)：221，254，359，372nm(ε53800，36600，26200，25300)。2%水溶液的Ph值为4。急性毒性LD50小鼠(rng/kg)：177.5腹腔注射，765.3口服。

用途抗肿瘤药。为DNA合成抑制剂。是喜树碱的半合成衍生物。

用途抗癌药。

用途抗肿瘤药。为DNA合成抑制剂。是喜树碱的半合成衍生物;用于制备盐酸伊立替康和盐酸伊立替康三水合物;抗癌药。

Chinese name: irinotecan
(S) -4,11-diethyl-3,4,4,14-tetrahydro-4-hydroxy-3,14-di 2-B) quinolin-9-yl ester; bis (p) -pyridine; (S) -4,11-bis Ethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-1H-pyran; irinotecan; (S) -4,11-diethyl- 4-hydroxy-3,14-dioxo-1H-pyrano [3 ', 4': 6,7] azepeno [1,2-B] quinoline -li-yl 1,4'-bipiperidine-1'-carboxylate; irinotecan sulphate; irinotecan (piconet); irinotecan (standard)
English name: Irinotecan
1-carboxylic acid (S) -4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-4-ene- 3,14-dioxo-1H-pyrano [3 ', 4': 6,7] indolizino [1,2-b] quinolin-9-yl ester; DQ-2805; (4S) -4,11-Diethyl- -hydroxy-9-[4-piperidinopiperidino carbonyl] oxy] -3,4,12,14-tetrahydro-1H-pyrano [3 ', 4': 6,7] indolizino [1,2-b] quinoline 17-diethyl-19-hydroxy-14,18-dioxo-17-oxa-3, 13-diazapentacyclo [11.8.0.0 ^ {2, (21), 2,4 (9), 5,7,10,15 (20) -heptaen-7-yl 4 (2) 4-hydroxy-3,14-dioxo-1H-pyrano [3 ' , 4 ': 6,7] indolizino [1,2-b] quinolin-9-yl- [1,4'-bipiperidine] -1'-carboxylic acid
CAS Number: 97682-44-5
Molecular formula: C33H39ClN4O6
Molecular weight: 623.14
EINECS number:
Anti-cancer drugs; anti-cancer drugs; anti-cancer drugs; anti-cancer drugs; anti-cancer drugs; anti-cancer drugs; anti-cancer drugs; anti-cancer drugs; Order a copy of this thesis The pharmaceutical intermediates, the semi-synthetic derivatives of camptothecin, and the semi-synthetic derivatives of camptothecin, Anti-cancer; Inhibitors; small molecule inhibitors, natural products; pharmaceutical raw materials; pharmaceutical raw materials; DNA damage
Chemical properties of light yellow powder, the melting point of 222 ~ 223 ℃.
Irinotecan Hydrochloride: C33H38N4O6? HCl? 3H2O. [136572-09-3]. From the water was very light yellow needle crystal or crystalline powder, the melting point of 256.5 ℃. [α] D20 + 67.7 ° (C = 1, water). UV maximum absorption (ethanol): 221,254,359,372 nm (ε53800,36600,26200,25300). The Ph value of the 2% aqueous solution is 4. Acute Toxic LD50 Mice (rng / kg): 177.5 Intraperitoneal injection, 765.3 Oral.
Use Antitumor drugs. For DNA synthesis inhibitors. Is a semi-synthetic derivative of camptothecin.
Use anticancer drugs.
Use Antitumor drugs. For DNA synthesis inhibitors. Is a semi-synthetic derivative of camptothecin; for the preparation of irinotecan hydrochloride and irinotecan hydrochloride trihydrate; anti-cancer drugs.