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123629-42-5

123629-42-5 structure
123629-42-5 structure
  • Name: ethyl 4-(4-hydroxy-3-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
  • Chemical Name: ethyl 4-(4-hydroxy-3-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate (en)5-Pyrimidinecarboxylic acid, 1,2,3,4-tetrahydro-4-(4-hydroxy-3-methoxyphenyl)-6-methyl-2-oxo-, ethyl ester (en)
  • CAS Number: 123629-42-5
  • Molecular Formula: C15H18N2O5
  • Molecular Weight: 306.31
  • Catalog: Signaling Pathways Anti-infection HIV
  • Create Date: 2017-09-03 18:50:55
  • Modify Date: 2024-03-01 07:37:11
  • gp120-IN-2 (compound 4i) is a potent HIV-1 gp120 inhibitor with an IC50 of 7.5 µM and CC50 of 112.93 µM. gp120-IN-2 shows anti-HIV-1 activity. gp120-IN-2 shows cytotoxicity in a dose dependent manner in SUP-T1 cells[1].

Name ethyl 4-(4-hydroxy-3-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate (en)5-Pyrimidinecarboxylic acid, 1,2,3,4-tetrahydro-4-(4-hydroxy-3-methoxyphenyl)-6-methyl-2-oxo-, ethyl ester (en)
Synonyms 1,2,3,4-tetrahydro-3-quinolinamine
3-amino-1,2,3,4-tetrahydroquinoline
1,2,3,4-tetrahydroquinoline-3-amine
Description gp120-IN-2 (compound 4i) is a potent HIV-1 gp120 inhibitor with an IC50 of 7.5 µM and CC50 of 112.93 µM. gp120-IN-2 shows anti-HIV-1 activity. gp120-IN-2 shows cytotoxicity in a dose dependent manner in SUP-T1 cells[1].
Related Catalog
Target

HIV-1:7.5 μM (IC50)

HIV-1:112.93 μM (CC50)

References

[1]. Senapathi J, et al. Design, Synthesis, and Antiviral activity of 1,2,3,4-Tetrahydropyrimidine derivatives acting as novel entry inhibitors to target at "Phe43 cavity" of HIV-1 gp120. Bioorg Med Chem. 2021 Dec 15;52:116526.

Molecular Formula C15H18N2O5
Molecular Weight 306.31
Exact Mass 306.12200
PSA 96.89000
LogP 2.24940

~98%

123629-42-5 structure

123629-42-5

Literature: Alvim, Haline G. O.; De Lima, Tatiani B.; De Oliveira, Heibbe C. B.; Gozzo, Fabio C.; De MacEdo, Julio L.; Abdelnur, Patricia V.; Silva, Wender A.; Neto, Brenno A. D. ACS Catalysis, 2013 , vol. 3, # 7 p. 1420 - 1430
Precursor  3

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