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pd_meltingpoint:250-256 °C (dec.)
Appearance:Pale yellow to yellow crystalline powder
Purity:99%
Buy Quality Irinotecan hydrochloride trihydrate 136572-09-3 In Stock with Immediately Delivery We supply high quality Irinotecan hydrochloride trihydrate (CAS 136572-09-3), in stock, factory directly supply to clients, lower prices, more competitiveness.
Irinotecan hydrochloride trihydrate is Pale yellow to yellow crystalline powder, while it's Molecular Formula is C33H45ClN4O9. Irinotecan Hydrochloride Trihydrate is a DNA topoisomerase inhibitor.
The CAS number of Irinotecan hydrochloride trihydrate is 136572-09-3.
More information of Irinotecan hydrochloride trihydrate 136572-09-3 are:
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Synonyms |
[1,4'-Bipiperidine]-1'-carboxylicacid,(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-ylester, monohydrochloride, trihydrate (9CI);[1,4'-Bipiperidine]-1'-carboxylicacid,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-ylester, monohydrochloride, trihydrate, (S)-;Irinotecan hydrochloridehydrate; |
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CAS Number |
136572-09-3 |
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Molecular Formula |
C33H45ClN4O9 |
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Molecular Weight |
677.195 |
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Density |
== |
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Melting Point |
250-256 °C (dec.) |
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Boiling Point |
873.4 °C at 760 mmHg |
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Flash Point |
482 °C |
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HS CODE |
29349990 |
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PSA |
141.89000 |
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LogP |
4.57600 |
Irinotecan (136572-09-3) is a semi-synthetic derivative of camptothecin (Cat.# 10-1041) that is an FDA approved anticancer drug. It is a prodrug that is converted by tissue esterases to 7-ethyl-10-hydroxycamptothecin (SN-38, Cat.# 10-2425), a potent inhibitor of DNA topoisomerase I.1,2 Although irinotecan is also a topoisomerase inhibitor, SN-38 is approximately 1000 times as potent in purified enzyme studies. In vitro cytotoxicity assays show much greater variability in potency between the two (2-2000 fold).3
InChI:InChI=1/C33H38N4O6.ClH/c1-3-22-23-9-8-21(43-32(40)36-14-10-20(11-15-36)35-12-6-5-7-13-35)16-27(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;1H/t33-;/m0./s1
Articles related to Irinotecan hydrochloride trihydrate:
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Article |
Source |
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Synthesis method of irinotecan hydrochloride |
- Paragraph 0026-0028, (2021/07/17) |
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