Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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T614542-5mg | 5mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $1,334.90 | |
T614542-25mg | 25mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $2,001.90 |
Synonyms | Jb-11 | NCGC00161419-03 | TRIMETREXATE [USAN] | 5-methyl-6-{[(3,4,5-trimethoxyphenyl)amino]methyl}quinazoline-2,4-diamine | TRIMETREXATE [MI] | 2,4-Quinazolinediamine,5-methyl-6-[[(3,4,5-trimethoxyphenyl)amino]methyl]- | BDBM18268 | SCHEMBL3983 | NSC 2490 |
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Specifications & Purity | Moligand™ |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of dihydrofolate reductase |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | 5-methyl-6-[(3,4,5-trimethoxyanilino)methyl]quinazoline-2,4-diamine |
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INCHI | InChI=1S/C19H23N5O3/c1-10-11(5-6-13-16(10)18(20)24-19(21)23-13)9-22-12-7-14(25-2)17(27-4)15(8-12)26-3/h5-8,22H,9H2,1-4H3,(H4,20,21,23,24) |
InChi Key | NOYPYLRCIDNJJB-UHFFFAOYSA-N |
Canonical SMILES | CC1=C(C=CC2=C1C(=NC(=N2)N)N)CNC3=CC(=C(C(=C3)OC)OC)OC |
Isomeric SMILES | CC1=C(C=CC2=C1C(=NC(=N2)N)N)CNC3=CC(=C(C(=C3)OC)OC)OC |
Alternate CAS | 72828-03-6,52128-35-5 |
PubChem CID | 5583 |
NSC Number | 249008 |
MeSH Entry Terms | CI 898;CI-898;CI898;Hydrate, Trimetrexate;JB 11;JB-11;JB11;Monohydrate, Monoacetate Trimetrexate;NSC 249008;NSC 328564;NSC-249008;NSC-328564;NSC249008;NSC328564;Trimetrexate;Trimetrexate Hydrate;Trimetrexate Monohydrate, Monoacetate |
Molecular Weight | 369.4 |
ChEMBL Ligand | CHEMBL119 |
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PubChem CID | 5583 |
CAS Registry No. | 52128-35-5 |
DrugBank Ligand | DB01157 |
Wikipedia | Trimetrexate |
DrugCentral Ligand | 2757 |
Enter Lot Number to search for COA:
1. Smith HO, Blessing JA, Vaccarello L. (2002) Trimetrexate in the treatment of recurrent or advanced leiomyosarcoma of the uterus: a phase II study of the Gynecologic Oncology Group.. Gynecol Oncol, 84 (1): (140-4). [PMID:11748990] [10.1021/op500134e] |
2. Sarris AH, Phan A, Duvic M, Romaguera J, McLaughlin P, Mesina O, King K, Medeiros LJ, Rassidakis GZ, Samuels B et al.. (2002) Trimetrexate in relapsed T-cell lymphoma with skin involvement.. J Clin Oncol, 20 (12): (2876-80). [PMID:12065565] [10.1021/op500134e] |
3. Wong BK, Woolf TF, Chang T, Whitfield LR. (1990) Metabolic disposition of trimetrexate, a nonclassical dihydrofolate reductase inhibitor, in rat and dog.. Drug Metab Dispos, 18 (6): (980-6). [PMID:1981548] [10.1021/op500134e] |
4. Sattler FR, Allegra CJ, Verdegem TD, Akil B, Tuazon CU, Hughlett C, Ogata-Arakaki D, Feinberg J, Shelhamer J, Lane HC et al.. (1990) Trimetrexate-leucovorin dosage evaluation study for treatment of Pneumocystis carinii pneumonia.. J Infect Dis, 161 (1): (91-6). [PMID:2136905] [10.1021/op500134e] |
5. Stewart JA, McCormack JJ, Tong W, Low JB, Roberts JD, Blow A, Whitfield LR, Haugh LD, Grove WR, Lopez AJ et al.. (1988) Phase I clinical and pharmacokinetic study of trimetrexate using a daily x5 schedule.. Cancer Res, 48 (17): (5029-35). [PMID:2970294] [10.1021/op500134e] |