General Information of Drug (ID: DMA2UYE)

Drug Name
Ro-24-7429 Drug Info
Indication
Disease Entry ICD 11 Status REF
Human immunodeficiency virus infection 1C62 Phase 2 [1]
Cross-matching ID
PubChem CID
135422895
ChEBI ID
CHEBI:93522
CAS Number
CAS 139339-45-0
TTD Drug ID
DMA2UYE

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Discontinued Drug(s)
Investigative Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Penicillamine DM40EF6 Cystinuria 5C60.2 Approved [3]
ALX-40-4C DMV934L Human immunodeficiency virus infection 1C62 Phase 2 [4]
Anti-HIV ribozyme therapy DMQZJ3B Human immunodeficiency virus infection 1C62 Phase 1/2 [5]
EM-2487 DMG9R8E Human immunodeficiency virus infection 1C62 Terminated [6]
Durhamycin A DM29PTO Discovery agent N.A. Investigative [7]
CGP 40336A DMEA5BZ Discovery agent N.A. Investigative [8]
⏷ Show the Full List of 6 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Human immunodeficiency virus Tat protein (HIV tat) TTT3ZC9 TAT_HV1H2 Modulator [2]

References

1 ClinicalTrials.gov (NCT00002314) A Study of Ro 24-7429 in Patients With HIV-Related Kaposi's Sarcoma. U.S. National Institutes of Health.
2 A randomized trial of the activity and safety of Ro 24-7429 (Tat antagonist) versus nucleoside for human immunodeficiency virus infection. The AIDS Clinical Trials Group 213 Team. J Infect Dis. 1995 Nov;172(5):1246-52.
3 Docking studies reveal a selective binding of D-penicillamine to the transactivator protein of human immunodeficiency virus type 1. FEBS Lett. 2002 Apr 10;516(1-3):43-6.
4 Anti-human immunodeficiency virus type 1 activity of an oligocationic compound mediated via gp120 V3 interactions. J Virol. 1996 May;70(5):2825-31.
5 Clinical gene therapy research utilizing ribozymes: application to the treatment of HIV/AIDS. Methods Mol Biol. 2004;252:581-98.
6 EM2487, a novel anti-HIV-1 antibiotic, produced by Streptomyces sp. Mer-2487: taxonomy, fermentation, biological properties, isolation and structure elucidation. J Antibiot (Tokyo). 1999 Nov;52(11):971-82.
7 Durhamycin A, a potent inhibitor of HIV Tat transactivation. J Nat Prod. 2002 Aug;65(8):1091-5.
8 RNA as a target for small molecules. Curr Opin Chem Biol. 2000 Dec;4(6):678-86.