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Reverse Transcriptase

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Reverse Transcriptase

Chemical Structure Cat. No. Product Name CAS No.
R-10015 Chemical Structure
BCP37585 R-10015 2097938-51-5
R-10015, a broad-spectrum antiviral compound for HIV infection, acts as a potent and selective inhibitor of LIM domain kinase (LIMK) and binds to the ATP-binding pocket, with an IC50 of 38 nM for human LIMK1.
Nevirapine Chemical Structure
BCP05587 Nevirapine 129618-40-2
Nevirapine is a non-nucleoside inhibitor of HIV-1 reverse transcriptase used to treat and prevent HIV/AIDS; with a Ki of 270 μM.
Ro 0335 Chemical Structure
BCP28161 Ro 0335 867365-76-2
Ro-0335 is a novel diphenylether nonnucleoside reverse transcriptase inhibitor.
AVX754 Chemical Structure
BCP07907 AVX754 160707-69-7
Apricitabine, also known as (-)-BCH-10652; (-)-dOTC; AVX-754; BCH-10618; SPD-754, is an experimental nucleoside reverse transcriptase inhibitor (NRTI) against HIV.
Foscarnet sodium Chemical Structure
BCP14044 Foscarnet sodium 63585-09-1
Foscarnet Sodium inhibits viral RNA polymerases, reverse transcriptase, and DNA polymerases through noncompetitive inhibition with dNTPs.
Zidovudine Chemical Structure
BCP03622 Zidovudine 30516-87-1
Zidovudine (Retrovir) is a reverse transcriptase inhibitor.
Fangchinoline Chemical Structure
BCP26186 Fangchinoline 436-77-1
Fangchinoline is an isolate from Stephania Tetrandra that shows anti-cancer activity. It inhibits breast adenocarcinoma proliferation through apoptosis induction. In addition, it has been shown to inhibit HIV-Type 1 replication.
Entecavir Chemical Structure
BCP02292 Entecavir 142217-69-4
Entecavir is a deoxyguanosine nucleoside analogue with antiviral activity against the hepatitis B virus (HBV).
Entecavir hydrate Chemical Structure
BCP01930 Entecavir hydrate 209216-23-9
Entecavir is a nucleoside analog that inhibits reverse transcription.
Pyridoxal hydrochloride Chemical Structure
BCP09066 Pyridoxal hydrochloride 65-22-5
Pyridoxal is one of the three natural forms of vitamin B6, along with pyridoxamine and pyridoxine.
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