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pd_meltingpoint:176-180 °C
Appearance:yellow crystalline powder
Purity:99%
Purity 99% Min Raltitrexed 112887-68-0 Spot Supply with Safe Transportation We supply high quality Raltitrexed (CAS 112887-68-0), in stock, factory directly supply to clients, lower prices, more competitiveness.
Raltitrexed is yellow crystalline powder, while it's Molecular Formula is C21H22N4O6S. Folate-based inhibitor of thymidylate synthase; rapidly and extensively metabolized to its more potent polyglutamate derivatives. Antineoplastic
The CAS number of Raltitrexed is 112887-68-0.
More information of Raltitrexed 112887-68-0 are:
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Synonyms |
D1694;Tomudex (TN);L-Glutamic acid,N-[[5-[[(1,4-dihydro-2- methyl-4-oxo-6-quinazolinyl)methyl]methylamino]- 2-thienyl]carbonyl]-;ZD1694;Raltitrexed (JAN/USAN);D 1694;(2S)-2-[[5-[methyl-[(2-methyl-4-oxo-1H-quinazolin-6-yl)methyl]amino]thiophene-2-carbonyl]amino]pentanedioic acid;L-Glutamic acid, N-((5-(((1,4-dihydro-2-methyl-4-oxo-6-quinazolinyl)methyl)methylamino)-2-thienyl)carbonyl)-;Tomudex;ICI-D1694;ICI D1694;N-(5-(N-(3,4-Dihydro-2-methyl-4-oxoquinazolin-6-ylmethyl)-N-methylamino)-2-thenoyl)-L-glutamic acid;(S)-2-[(1-{5-[Methyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-thiophen-2-yl}-methanoyl)-amino]-pentanedioic acid;ZD 1694;D-1694; |
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CAS Number |
112887-68-0 |
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Molecular Formula |
C21H22N4O6S |
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Molecular Weight |
458.495 |
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Density |
1.49 g/cm3 |
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Melting Point |
176-180 °C |
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PSA |
180.93000 |
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LogP |
2.36810 |
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Pka |
3.50±0.10(Predicted) |
Tomudex was launched in Ireland, France, Luxembourg and the UK for advanced colorectal cancer and it was prepared in a convergent manner (6 steps) from diethyl L-glutamate and 6-bromomethyi-2-methyl-quinazolin4(3H)-one. Tomudex is a highly selective inhibitor of thymidylate synthase (TS), the key enzyme in the biochemical conversion of dUMP to dTMP. It enters the cell via the reduced folatefmethotrexate cell membrane carrier and is converted to the polyglutamate species by folylpolyglutamate synthase within 4h where it then binds to the folate substrate site of TS. Clinically, it had a 29% response rate in patients with advanced colorectal cancer. It is water soluble, can be administered as a single dose every three weeks and had no hepto- or nephrotoxicity.
InChI:InChI=1/C20H24N4O2S/c1-12-21-15-7-6-13(10-14(15)18(25)22-12)11-24(5)17-9-8-16(27-17)19(26)23-20(2,3)4/h6-10H,11H2,1-5H3,(H,23,26)(H,21,22,25)
Articles related to Raltitrexed:
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Article |
Source |
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New synthesis of thymidylate synthase inhibitor raltitrexed |
Cao, Sheng-Li,Wan, Rong,Feng, Yu-Ping , p. 3519 - 3526 (2003) |
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Raltitrexed pharmaceutical composition and preparation method thereof |
- Paragraph 0090; 0091, (2018/04/02) |
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