| Weight | 456.572 g/mol |
|---|---|
| Formula | C22H28N6O3S |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 6 |
Delavirdine (136817-59-9)
Score:
#280 in Microbiology
,
#2450 in Biology
,
#3051 in Chemistry
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- Novel 1,5-diphenylpyrazole nonnucleoside HIV-1 reverse transcriptase inhibitors with enhanced activity versus the delavirdine-resistant P236L mutant : Lead identification and SAR of 3- and 4-substituted derivatives (Journal of Medicinal Chemistry, 2000)
- Transport of stavudine, delavirdine, and saquinavir across the bloodbrain barrier by polybutylcyanoacrylate, methylmethacrylate-sulfopropylmethacrylate, and solid lipid nanoparticles (International Journal of Pharmaceutics, 2007)
- The P236L delavirdine-resistant human immunodeficiency virus type 1 mutant is replication defective and demonstrates alterations in both RNA 5'-end- and DNA 3'-end-directed RNase H activities. (Journal of Virology, 1999)
- Amino Acid Substitutions at Position 190 of Human Immunodeficiency Virus Type 1 Reverse Transcriptase Increase Susceptibility to Delavirdine and Impair Virus Replication (Journal of Virology, 2003)
- Randomized Study of Saquinavir with Ritonavir or Nelfinavir Together with Delavirdine, Adefovir, or Both in Human Immunodeficiency Virus-Infected Adults with Virologic Failure on Indinavir: AIDS Clinical Trials Group Study 359 (The Journal of Infectious Diseases, 2000)
- Interactions between Buprenorphine and Antiretrovirals. I. The Nonnucleoside Reverse-Transcriptase Inhibitors Efavirenz and Delavirdine (Clinical Infectious Diseases, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)NC1=C(N=CC=C1)N2CCN(CC2)C(=O)C3=CC4=C(N3)C=CC(=C4)NS(=O)(=O)C
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InChIKeyWHBIGIKBNXZKFE-UHFFFAOYSA-N
- Pubchem - Delavirdine
- Wikipedia - delavirdine
Delavirdine (DLV) (brand name Rescriptor) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) marketed by ViiV Healthcare. It is used as part of highly active antiretroviral therapy (HAART) for the treatment of human immunodeficiency virus (HIV) type 1. It is presented as the mesylate.
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