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Irinotecan

CAS No.
97682-44-5
Chemical Name:
Irinotecan
Synonyms
CPT-11;IRINOTECAN HCL;CAMPTOSAR;Irinotecan(TECANS);Irinotecan (free Base);[1,4'-BIPIPERIDINE]-1'-CARBOXYLIC ACID;(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;DQ-2805;SN-38-11;IRINOTECAN
CBNumber:
CB1124156
Molecular Formula:
C33H38N4O6
Molecular Weight:
586.68
MDL Number:
MFCD01862255
MOL File:
97682-44-5.mol
MSDS File:
SDS
Last updated:2023-09-07 18:57:57

Irinotecan Properties

Melting point 222-223°
Boiling point 873.4±65.0 °C(Predicted)
Density 1.40±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility Acetonitrile (Slightly, Heated, Sonicated), DMSO (Slightly), Methanol (Slightly)
pka 11.20±0.20(Predicted)
form Solid
color White to Brown
CAS DataBase Reference 97682-44-5(CAS DataBase Reference)
FDA UNII 7673326042
NCI Dictionary of Cancer Terms Camptosar; CPT 11
NCI Drug Dictionary Camptosar
ATC code L01CE02

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08,GHS05
Signal word  Danger
Hazard statements  H315-H361-H302-H318-H373
Precautionary statements  P264-P270-P301+P312-P330-P501-P201-P202-P281-P308+P313-P405-P501-P260-P314-P501-P264-P280-P302+P352-P321-P332+P313-P362-P280-P305+P351+P338-P310
Hazard Codes  Xn
Risk Statements  22
RTECS  DW1061000

Irinotecan price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Tocris 2688 CPT11 ≥99%(HPLC) 97682-44-5 10 $229 2021-12-16 Buy
Tocris 2688 CPT11 ≥99%(HPLC) 97682-44-5 50 $960 2021-12-16 Buy
Usbiological 255047 CPT 11 97682-44-5 10mg $480 2021-12-16 Buy
TRC I767523 (+)-Irinotecan 97682-44-5 50mg $60 2021-12-16 Buy
Biosynth Carbosynth FI33814 Irinotecan 97682-44-5 100mg $60 2021-12-16 Buy
Product number Packaging Price Buy
2688 10 $229 Buy
2688 50 $960 Buy
255047 10mg $480 Buy
I767523 50mg $60 Buy
FI33814 100mg $60 Buy

Irinotecan Chemical Properties,Uses,Production

Uses

Irinotecan is a topoisomerase I inhibitor for LoVo cells and HT-29 cells with IC50 of 15.8 μM and 5.17 μM, respectively

Uses

(+)-Irinotecan is a Topo I inhibitor.

Definition

ChEBI: A member of the class of pyranoindolizinoquinolines that is the carbamate ester obtained by formal condensation of the carboxy group of [1,4'-bipiperidine]-1'-carboxylic acid with the phenolic hydroxy group of (4S)-4,11-diethyl-4,9-dihydro y-1H-pyrano[3',4':6,7]indolizino[1,2- hydrochloride]quinoline-3,14-dione. Used (in the form of its hydrochloride salt trihydrate) in combination with fluorouracil and leucovorin, for the treatment of patients with metastatic adenocarcino a of the pancreas after disease progression following gemcitabine-based therapy. It is converted via hydrolysis of the carbamate linkage to its active metabolite, SN-38, which is ~1000 times more active.

brand name

Camptosar (Pharmacia &Upjohn) .

Biological Activity

irinotecan (cpt-11), a prodrug for treating metastatic colorectal cancer, is a topoisomerase i inhibitor for lovo cells and ht-29 cells with ic50 of 15.8 μm and 5.17 μm, respectively [1].in vivo, irinotecan is converted to sn-38, its most active metabolite, by carboxylesterase converting enzyme (cce) [2].

in vitro

irinotecan induced similar amounts of cleavable complexes in lovocells and ht-29 cell lines with the ic50 of 15.8 μm and 5.17 μm, respectively [1].after addition of 157 mm irinotecan to plasma, sn-38 concentration showed linear increase during the first 60-min period, followed by a plateau.in the first 60 min, mean and standard deviation of the conversion rate were 515.9 ± 50.1 pmol/ml/h (n = 69), with a coefficient of variation of 0.097 [2]. irinotecan (cpt-11) was significantly more active in sclc than in nsclccelllines (p = 0.0036). ce activity appeared to be associated with higher sensitivity to cpt-11 in human lung cancercelllines and may partly explain the difference in the in vitro sensitivity to cpt-11 between sclc and nsclccells [3].in vitro, the sensitivity to cpt-11 and sn-38 was highest in ls174t and colo 320cells, intermediate in sw1398cellsand lowest in colo 205 and widr cells. the activity of sn-38 was 130 to 570 times than cpt-11[4].

in vivo

in colo 320 xenografts, irinotecan induced a maximum growth inhibition of 92% [4].a single dose of irinotecan significantly increased amounts of topoisomerase i covalently bound to dna in stomach, duodenum, colon and liver. concomitantly, the irinotecan-treated group exihibited significantly higher amounts of dna strand breaks in colon mucosa cells compared to the control group [5].

References

[1]. tobin p, clarke s, seale j p, et al. the in vitro metabolism of irinotecan (cpt‐11) by carboxylesterase and β‐glucuronidase in human colorectal tumours[j]. british journal of clinical pharmacology, 2006, 62(1): 122-129.
[2]. shingyoji m, takiguchi y, watanabe‐uruma r, et al. in vitro conversion of irinotecan to sn‐38 in human plasma[j]. cancer science, 2004, 95(6): 537-540.
[3]. van ark-otte j, kedde m a, van der vijgh w j, et al. determinants of cpt-11 and sn-38 activities in human lung cancer cells[j]. british journal of cancer, 1998, 77(12): 2171.
[4]. jansen w j m, zwart b, hulscher s t m, et al. cpt-11 in human colon-cancer cell lines and xenografts: characterization of cellular sensitivity determinants[j]. international journal of cancer, 1997, 70(3): 335-340.
[5]. na y s, jung k a, kim s m, et al. the histone deacetylase inhibitor pxd101 increases the efficacy of irinotecan in in vitro and in vivo colon cancer models[j]. cancer chemotherapy and pharmacology, 2011, 68(2): 389-398.

Irinotecan Preparation Products And Raw materials

Global( 403)Suppliers
Supplier Tel Email Country ProdList Advantage
Hangzhou ICH Biofarm Co., Ltd
+undefined8613073685410 sales@ichemie.com China 985 58
Shaanxi Haibo Biotechnology Co., Ltd
+undefined18602966907 qinhe02@xaltbio.com China 1000 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21695 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9350 55
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070 product@chemlin.com.cn CHINA 3012 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3620 58
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 967 58

Related articles

View Lastest Price from Irinotecan manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
lrinotecan pictures 2024-04-12 lrinotecan
97682-44-5
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
Irinotecan pictures 2023-11-01 Irinotecan
97682-44-5
US $0.00-0.00 / kg 1kg 99.9% 20 tons Hangzhou ICH Biofarm Co., Ltd
Irinotecan pictures 2023-06-15 Irinotecan
97682-44-5
US $825.00 / g/Bag 10g 99% 1kg Baoji Guokang Bio-Technology Co., Ltd.
  • lrinotecan pictures
  • lrinotecan
    97682-44-5
  • US $0.00 / kg
  • 99%
  • Shaanxi Haibo Biotechnology Co., Ltd
  • Irinotecan pictures
  • Irinotecan
    97682-44-5
  • US $0.00-0.00 / kg
  • 99.9%
  • Hangzhou ICH Biofarm Co., Ltd
  • Irinotecan pictures
  • Irinotecan
    97682-44-5
  • US $825.00 / g/Bag
  • 99%
  • Baoji Guokang Bio-Technology Co., Ltd.

Irinotecan Spectrum

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 [1,4'-Bipiperidine]-1'-carboxylic acid, 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, (S)- 1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline, [1,4'-bipiperidine]-1'-carboxylic acid deriv. Irinotecan base (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 (s)-[1,4'-bipiperidine]-1'-carboxylic acid, 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 hydrochloride (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 Irinotecan Labeled d10 (S)-4,11-Diethyl-4-hydroxy-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2- TOPOTECIN HYDROCHLORIDE IRINOTECAN CAMPTOTHECIN 11 HYDROCHLORIDE CAMPTOTHECIN 11 HYDROCHLORIDE,TOPOTECIN Irinotecan(Cpt-11) (1,4'-Bipiperidine)-1'-carboxylicacid(S)-4,11-di] Irinotecane [1,4'-Bipiperidine]-1'-carboxylic acid, (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 ester IRINOTECAN HCL(P) [1,4'-Bipiperidine]-1'-carboxylic acid, (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 ester (9CI) Irinotecan USP/EP/BP (S)-4,11-Diethyl-4-hydroxy-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl [1,4'-bipiperidine]-1'-carboxylate Irinotecan EP Impurity L Irinotecan Monomer Irinotecanum IrinotecanQ: What is Irinotecan Q: What is the CAS Number of Irinotecan Q: What is the storage condition of Irinotecan Q: What are the applications of Irinotecan Irinotecan (free Base) [1,4'-BIPIPERIDINE]-1'-CARBOXYLIC ACID CPT-11 IRINOTECAN HCL CAMPTOSAR Irinotecan(TECANS) (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 Propanamide,N-(3-bromophenyl)-8-chloro- (S)-4,11-Diethyl-4-hydroxy-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl [1,4'-bipiperidine]-1'-carboxylate 97682-44-5 97682-44-8 C33H38N4O6 Camptothecin series APIs Natural Anti-cancer Medical Materials and It's Derivatives API's chemical reagent pharmaceutical intermediate phytochemical reference standards from Chinese medicinal herbs (TCM). standardized herbal extract API Anti cancer Inhibitors Camptosar, Campto Anti-cancer&immunity