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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H27N9O6
Molecular Weight 573.56
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TALOTREXIN

SMILES

NC1=NC(N)=C2N=C(CNC3=CC=C(C=C3)C(=O)N[C@@H](CCCNC(=O)C4=C(C=CC=C4)C(O)=O)C(O)=O)C=NC2=N1

InChI

InChIKey=NYQPLPNEESYGNO-IBGZPJMESA-N
InChI=1S/C27H27N9O6/c28-21-20-22(36-27(29)35-21)32-13-16(33-20)12-31-15-9-7-14(8-10-15)23(37)34-19(26(41)42)6-3-11-30-24(38)17-4-1-2-5-18(17)25(39)40/h1-2,4-5,7-10,13,19,31H,3,6,11-12H2,(H,30,38)(H,34,37)(H,39,40)(H,41,42)(H4,28,29,32,35,36)/t19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C27H27N9O6
Molecular Weight 573.56
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Talotrexin (also known as PT-523) was developed as a nonpolyglutamatable antifolate drug for the treatment of various types of tumors. It is known that antifolates are a class of cytotoxic or antineoplastic agents, which inhibit or prevent the maturation and proliferation of malignant cells. Talotrexin was studied in clinical trials for the treatment of brain and central nervous system tumors, leukemia, lymphoma, unspecified childhood solid tumor. However, this study was withdrawn because of toxicity. In addition, was studied in phase I/II multicenter clinical trial in patients with non-small-cell Lung carcinoma, this study was also withdrawn. The withdrawal was related to incidences of dose-limiting mucositis and myelosuppression. However, on May 22, 2006, was announced that the U.S. Food and Drug Administration has granted orphan drug designation for talotrexin in patients with acute lymphoblastic leukemia (ALL).

Approval Year

PubMed

PubMed

TitleDatePubMed
Treatment of acute lymphoblastic leukaemia : a new era.
2007
Emerging therapeutic options for Philadelphia-positive acute lymphocytic leukemia.
2007 Mar
Clinical potency of methotrexate, aminopterin, talotrexin and pemetrexed in childhood leukemias.
2010 May
Cancer chemotherapy: targeting folic acid synthesis.
2010 Nov 19

Sample Use Guides

10 mg/m2 dose of PT523 administered day 1 of a 28-day cycle as a 5 minute IV infusion (IV bolus)
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:04:08 UTC 2023
Edited
by admin
on Fri Dec 15 16:04:08 UTC 2023
Record UNII
A8E516A20K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TALOTREXIN
INN   WHO-DD  
INN  
Official Name English
NSC-633713
Code English
2-(((4S)-4-CARBOXY-4-((4-(((2,4-DIAMINOPTERIDIN-6-YL)METHYL)AMINO)BENZOYL)AMINO)BUTYL)CARBAMOYL)BENZOIC ACID
Systematic Name English
talotrexin [INN]
Common Name English
BENZOIC ACID,2-((((4S)-4-CARBOXY-4-((4-(((2,4-DIAMINO-6-PTERIDINYL)METHYL)AMINO)BENZOYL)AMINO)BUTYL)AMINO)CARBONYL)-
Common Name English
NSC-623017
Code English
Talotrexin [WHO-DD]
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 221306
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
NCI_THESAURUS C2153
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
NCI_THESAURUS C511
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
Code System Code Type Description
FDA UNII
A8E516A20K
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
NCI_THESAURUS
C29341
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
NSC
633713
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
PUBCHEM
130731
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
INN
8622
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
ChEMBL
CHEMBL590985
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
DRUG BANK
DB06178
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
NSC
623017
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
SMS_ID
300000037016
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
CAS
113857-87-7
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
MESH
C085590
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
EPA CompTox
DTXSID20921223
Created by admin on Fri Dec 15 16:04:08 UTC 2023 , Edited by admin on Fri Dec 15 16:04:08 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY