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Raltitrexed

Raltitrexed

CAS: 112887-68-0

Molecular Formula: C21H22N4O6S

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Raltitrexed - Names and Identifiers

Name Raltitrexed
Synonyms ZD-1694
Tomudex
ICI-D-1694
RALTITREXED
Raltitrexed
N-(1,1-dimethylethyl)-5-[methyl-[(2-methyl-4-oxo-3H-quinazolin-6-yl)methyl]amino]thiophene-2-carboxamide
N-[[5-[[(1,4-Dihydro-2-methyl-4-oxo-6-quinazolinyl)methyl]methylamino]-2-thienyl]carbonyl]-L-glutamic Acid
2-[5-[(4-hydroxy-2-methyl-quinazolin-6-yl)methyl-methyl-amino]thiophen-2-yl]carbonylaminopentanedioic acid
L-Glutamic acid, N-[[5-[[(3,4-dihydro-2-methyl-4-oxo-6-quinazolinyl)methyl]methylamino]-2-thienyl]carbonyl]-
N-[(5-{methyl[(2-methyl-4-oxo-1,4-dihydroquinazolin-6-yl)methyl]amino}thiophen-2-yl)carbonyl]-L-glutamic acid
(S)-2-(5-(METHYL((2-METHYL-4-OXO-3,4-DIHYDROQUINAZOLIN-6-YL)METHYL)AMINO)THIOPHENE-2-CARBOXAMIDO)PENTANEDIOIC ACID
(s)-2-[(1-{5-[methyl-(2-methyl-4-oxo-3,4-dihydro-quinazolin-6-ylmethyl)-amino]-thiophen-2-yl}-methanoyl)-amino]-pentanedioic acid
CAS 112887-68-0
EINECS 652-997-2
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)
InChIKey IVTVGDXNLFLDRM-HNNXBMFYSA-N

Raltitrexed - Physico-chemical Properties

Molecular FormulaC21H22N4O6S
Molar Mass458.49
Density1.49±0.1 g/cm3(Predicted)
Melting Point176-1800C
Solubility DMSO : ≥ 20 mg/mL mother liquor preservation: sub-package and freeze storage to avoid repeated freezing and thawing;-20 ℃,1 month;-80 ℃,6 months (after dilution, the solution temperature is low and storage may precipitate, as far as possible to use the current preparation) Cell experiment: dissolve with DMSO first: dilute with culture medium then, and the dilution process is recommended to be carried out in stages to avoid too fast concentration change leading to compound precipitation. If the compound is precipitated during the dilution process, it can be redissolved by ultrasound. During dilution, ensure that the final concentration of DMSO in the working fluid should be below 0.1% as far as possible, and the maximum should not exceed 0.5%, and set up a DMSO control group with corresponding concentration. Animal experiment: Dissolve with DMSO first: dilute with water or normal saline, etc. The dilution process is recommended to be carried out in sections to avoid excessive concentra
Appearancesolid
Coloroff-white to light yellow
pKa3.50±0.10(Predicted)
Storage Condition2-8°C
Refractive Index1.638
MDLMFCD12828867
Physical and Chemical PropertiesLight yellow powder. Soluble in water. Monohydrate: C2lH22N4O6S? H2O. Melting point 180-184 °c.
UseStrong inhibitory effect on colon cancer cell lines
TargetThymidylate synthase

Raltitrexed - Risk and Safety

Risk CodesR36/38 - Irritating to eyes and skin.
R25 - Toxic if swallowed
R61 - May cause harm to the unborn child
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37/39 - Wear suitable gloves and eye/face protection
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S53 - Avoid exposure - obtain special instructions before use.
UN IDsUN 2811 6.1 / PGIII
WGK Germany2

Raltitrexed - Reference

Reference
Show more
1: Surmont VF, van Meerbeeck JP. Raltitrexed in mesothelioma. Expert Rev Anticancer Ther. 2011 Oct;11(10):1481-90. Review. PubMed PMID: 21999120.
2: Wilson KS, Malfair Taylor SC. Raltitrexed: optimism and reality. Expert Opin Drug Metab Toxicol. 2009 Nov;5(11):1447-54. Review. PubMed PMID: 19863453.
3: Hind D, Tappenden P, Tumur I, Eggington S, Sutcliffe P, Ryan A. The use of irinotecan, oxaliplatin and raltitrexed for the treatment of advanced colorectal cancer: systematic review and economic evaluation. Health Technol Assess. 2008 May;12(15):iii-ix, xi-162. Review. PubMed PMID: 18462574.
4: Cao S, Bhattacharya A, Durrani FA, Fakih M. Irinotecan, oxaliplatin and raltitrexed for the treatment of advanced colorectal cancer. Expert Opin Pharmacother. 2006 Apr;7(6):687-703. Review. PubMed PMID: 16556086.
5: Van Cutsem E, Cunningham D, Maroun J, Cervantes A, Glimelius B. Raltitrexed: current clinical status and future directions. Ann Oncol. 2002 Apr;13(4):513-22. Review. PubMed PMID: 12056700.

Raltitrexed - Nature

Open Data Verified Data

light yellow powder. Soluble in water. Raltitrexed Monohydrate: C21H22 N406 S.H2 0. Light grass green powder. Melting Point 18 0~184 deg C.

Last Update:2025-06-10 22:55:16

Raltitrexed - Preparation Method

Open Data Verified Data

2,6-= methyl -4(3H)-quinazolinone was alkylated with tert-pentalyloxymethyl chloride and then bromonated with N-bromosuccinimide, 6-(bromomethyl) -2-methyl -3-[(tert-valeryloxy) methyl]-4(3H)-quinazolinone is obtained. The material and N-[5-methylaminothiophene-2-carbonyl]-L-glutamic acid Diethyl ester condensation, product and sodium hydroxide in ethanol solution at room temperature stirring hydrolysis, and simultaneous deprotection, then acidification results in raltitrexed.

Last Update:2025-06-10 22:55:16

Raltitrexed - Preparation solution concentration reference

 1mg5mg10mg
1 mM2.181 ml10.905 ml21.811 ml
5 mM0.436 ml2.181 ml4.362 ml
10 mM0.218 ml1.091 ml2.181 ml
5 mM0.044 ml0.218 ml0.436 ml
Last Update:2024-01-02 23:10:35

Raltitrexed - Application

Open Data Verified Data

developed by Zeneca, UK, marketed under the trade name Tomudex in AstraZenca, UK, 1996. Thymidylate synthase inhibitor. For the treatment of colon cancer, rectal cancer. It is a new type of anticancer drug, which is mainly used in the first-line treatment of advanced colorectal cancer that is intolerant or not suitable for 5-Fu treatment.

Last Update:2025-08-19 16:24:40
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