Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Nolatrexed

From Wikipedia, the free encyclopedia
Nolatrexed
Names
Preferred IUPAC name
2-Amino-6-methyl-5-[(pyridin-4-yl)sulfanyl]quinazolin-4(1H)-one
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C14H12N4OS/c1-8-2-3-10-11(13(19)18-14(15)17-10)12(8)20-9-4-6-16-7-5-9/h2-7H,1H3,(H3,15,17,18,19) ☒N
    Key: XHWRWCSCBDLOLM-UHFFFAOYSA-N ☒N
  • InChI=1/C14H12N4OS/c1-8-2-3-10-11(13(19)18-14(15)17-10)12(8)20-9-4-6-16-7-5-9/h2-7H,1H3,(H3,15,17,18,19)
    Key: XHWRWCSCBDLOLM-UHFFFAOYAK
  • CC1=C(C2=C(C=C1)NC(=NC2=O)N)SC3=CC=NC=C3
Properties
C14H12N4OS
Molar mass284.34 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Nolatrexed is athymidylate synthase inhibitor.[1][2]

References

[edit]
  1. ^Hughes AN, Rafi I, Griffin MJ, et al. (January 1999)."Phase I studies with the nonclassical antifolate nolatrexed dihydrochloride (AG337, THYMITAQ) administered orally for 5 days".Clin. Cancer Res.5 (1):111–8.PMID 9918208.
  2. ^"Nolatrexed".PubChem.gov. Pub Chem. Retrieved12 August 2014.


This article about anEther is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Nolatrexed&oldid=1301020820"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp