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(±)Amethopterin hydrate_Molecular_structure_CAS_60388-53-6(anhydrous))
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(±)Amethopterin hydrate

Catalog No. A7019 Name Sigma Aldrich
CAS Number 60388-53-6(anhydrous) Website http://www.sigmaaldrich.com
M. F. C20H24N8O6 Telephone 1-800-521-8956
M. W. 472.45456 Fax
Purity ≥95% Email
Storage Chembase ID: 134377

SYNONYMS

IUPAC name
2-[(4-{[(2,4-diaminopteridin-6-yl)methyl](methyl)amino}phenyl)formamido]pentanedioic acid hydrate
IUPAC Traditional name
hydrate methotrexate
Synonyms
MTX
氨甲叶酸
氨甲喋呤
DL-4-Amino-N10-methylpteroylglutamic acid

DATABASE IDS

PubChem SID 24891167
EC Number 262-213-7
CAS Number 60388-53-6(anhydrous)
MDL Number MFCD00150845

PROPERTIES

Purity ≥95%
Gene Information human ... DHFRP1(573971), FPGS(2356), SLC19A1(6573), TYMS(7298)mouse ... Dhfr(13361)rat ... Dhfr(24312)
Apperance yellow to yellow with an orange cast powder
Solubility H2O: insoluble
Solubility NaOH: soluble (minimal amount of 0.1 N NaOH to solubilize, then dilute in neutral buffer or saline)
GHS Pictograms GHS06
GHS Pictograms GHS08
GHS Signal Word Danger
GHS Hazard statements H301-H315-H319-H360
European Hazard Symbols Toxic Toxic (T)
Personal Protective Equipment Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
GHS Precautionary statements P201-P301 + P310-P305 + P351 + P338-P308 + P313
RID/ADR UN 1544 6.1/PG 2
Risk Statements 61-25-36/38
RTECS MA1224100
Safety Statements 53-26-36/37-45
Storage Temperature -20°C
Hazard Class 6.1
UN Number 1544
Packing Group 2
German water hazard class 3

DETAILS

Description (简体中文)
包装
25 mg in poly bottle
500 mg in glass bottle
Reconstitution
Add a minimal amount of 0.1 N NaOH to solubilize, then dilute in neutral buffer or saline. Diluted stock is stable for 1 week refrigerated and for 1 month frozen at -20 °C. References: Cell & Tissue Culture: Laboratory Procedures, Chapter 27, Page 27D:3.2 (A. Doyle, et al., eds, John Wiley) and Cell Biology: A Laboratory Handbook, vol. 2, page 417 (Julio E. Celis, ed., Academic Press).
Application
Amethopterin is a folic acid antagonist and potent anticancer agent. Amethopterin blocks DNA synthesis by preventing the production of tetrahydrofolate cofactors which are required to make thymidine. Amethopterin is actively transported into cells by the folate transporter where it is converted to a high molecular weight polyglutamate metabolite by folylpolyglutamate synthase, a dihydrofolate reductase inhibitor.
Biochem/physiol Actions
Amethopterin is a folic acid antagonist and potent anticancer agent. Blocks DNA synthesis by blocking the production of tetrahydrofolate covactors required for the synthesis of thymidine. Amethopterin is actively transported into cells by the folate transporter. In the cell, it is converted to a high molecular weight polyglutamate metabolite by folylpolyglutamate synthase that, in turn, binds to dihydrofolate reductase and inhibits its activity. Amethopterin-polyglutamate is degraded intracellularly by γ-glutamyl hydrolase.

REFERENCES