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CAS No 97682-44-5 , Irinotecan

  • Name: Irinotecan
  • Synonyms: Irinotecanum; CPT-11; Irinotecan Hcl; Irinotecanum [INN-Latin];Irinotecan;Camptosar; Irinotecan hydrochloride; 97682-44-5; (+)-Irinotecan; IRINOTECAN;
  • CAS Registry Number:
  • Melting Point: 222-223 deg C
  • Density: 1.4 g/cm3
  • Water Solubility: soluble in water
  • Hazard Symbols: Xn: Harmful;
  • Molecular Weight: 586.67802
  • InchiKey: UWKQSNNFCGGAFS-XIFFEERXSA-N
  • InChI: InChI=1S/C33H38N4O6/c1-3-22-23-16-21(43-32(40)36-14-10-20(11-15-36)35-
    12-6-5-7-13-35)8-9-27(23)34-29-24(22)18-37-28(29)17-26-25(30(37)38)19-
    42-31(39)33(26,41)4-2/h8-9,16-17,20,41H,3-7,10-15,18-19H2,
    1-2H3/t33-/m0/s1
  • Risk Statements: 22.
  • Molecular Formula: C33H38N4O6
  • Molecular Structure:CAS No:97682-44-5 Irinotecan
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97682-44-5 Irinotecan hydrochloride

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97682-44-5 Irinotecan

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  • Address: 1213 JunMin Road,Pudong,China ,China
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  • China Kouting Chemical Co.,Ltd [Importer/Exporter]
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References of Irinotecan
Title: Irinotecan
CAS Registry Number: 97682-44-5
CAS Name: [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
Synonyms: 7-ethyl-10-[4-(1-piperidino)-1-piperidino]carbonyloxycamptothecin; (+)-7-ethyl-10-hydroxycamptothecine 10-[1,4¢-bipiperidine]-1¢-carboxylate; (+)-(4S)-4,11-diethyl-4-hydroxy-9-[(4-piperidinopiperidino)carbonyloxy]-1H-pyrano[3¢,4¢:6,7]indolizino[1,2-b]quinoline-3,14-(4H,12H)-dione
Molecular Formula: C33H38N4O6
Molecular Weight: 586.68
Percent Composition: C 67.56%, H 6.53%, N 9.55%, O 16.36%
Literature References: DNA topoisomerase I inhibitor. Semisynthetic derivative of camptothecin, q.v.; de-esterified in vivo to the active metabolite, 7-ethyl-10-hydroxycamptothecin (SN-38). Prepn: JP Kokai 85 19790; T. Miyasaka et al., US 4604463 (1985, 1986 both to Yakult Honsha); S. Sawada et al., Chem. Pharm. Bull. 39, 1446 (1991). Antitumor activity and toxicity data: T. Kunimoto et al., Cancer Res. 47, 5944 (1987). Mechanism of action study: Y. Kawato et al., ibid. 51, 4187 (1991). Clinical trial in colorectal cancer: J. Y. Douillard et al., Lancet 355, 1041 (2000). Review of pharmacology and clinical experience: N. Masuda et al., Crit. Rev. Oncol. Hematol. 24, 3-26 (1996); S. O'Reilly, E. K. Rowinsky, ibid. 47-70; of clinical toxicity: K. Seiter, Expert Opin. Drug Safety 4, 45-53 (2005).
Properties: Pale yellow powder, mp 222-223°.
Melting point: mp 222-223°
 
Derivative Type: Hydrochloride trihydrate
CAS Registry Number: 136572-09-3; 100286-90-6 (hydrochloride)
Manufacturers' Codes: CPT-11; DQ-2805
Trademarks: Campto (Sanofi-Aventis); Camptosar (Pharmacia & Upjohn)
Molecular Formula: C33H38N4O6.HCl.3H2O
Molecular Weight: 677.18
Percent Composition: C 58.53%, H 6.70%, N 8.27%, O 21.26%, Cl 5.24%
Properties: Slightly pale yellow needles or crystalline powder from water, mp 256.5°. [a]D20 +67.7° (c = 1 in water). uv max (ethanol): 221, 254, 359, 372 nm (e 53800, 36600, 26200, 25300). Slightly sol in water and organic solvents. pH of 2% aqueous soln = 4. LD50 in mice (mg/kg): 177.5 i.p.; 765.3 orally (Kunimoto).
Melting point: mp 256.5°
Optical Rotation: [a]D20 +67.7° (c = 1 in water)
Absorption maximum: uv max (ethanol): 221, 254, 359, 372 nm (e 53800, 36600, 26200, 25300)
Toxicity data: LD50 in mice (mg/kg): 177.5 i.p.; 765.3 orally (Kunimoto)
 
Therap-Cat: Antineoplastic.
Keywords: Antineoplastic; Alkaloids/Natural Products; Camptothecin Derivatives; Topoisomerase I Inhibitor.