Chemical structure
Cat.No.
Product Name
CAS no.
Target
Abacavir (ABC) is a powerful nucleoside analog reverse transcriptase inhibitor (NRTI) used to treat HIV and AIDS.
YN250118 Delavirdine 136817-59-9
Delavirdine (U 90152; BHAP-U 90152) is a potent, highly specific and orally activenon-nucleoside reverse transcriptaseinhibitor (NNRTI). Delavirdine selectively inhibits HIV-1 reverse transcriptase (RT) (IC50=0.26 μM...
YN251668 Tripterifordin 139122-81-9
Tripterifordin, isolated from the roots ofTripterygium wilfordii, possesses significant anti-HIVreplication activities in H9 lymphocyte cells with an EC50 value of 3100nM, respectively.
YN250881 Pentosan Polysulfate Sodium 140207-93-8
Pentosan Polysulfate Sodium is an orally bioavailable, semi-synthetic medication with anti-inflammatory and pro-chondrogenic properties. Pentosan Polysulfate Sodium also is a potent and selective anti-HIVagent. Pentosan Polys...
YN251833 HIV-1 Rev 34-50 141237-50-5
HIV-1 Rev (34-50) is a 17-aa peptide derived from the Rev-responsive element (RRE)-binding domains of Rev in HIV-1, with anti-HIV-1 activity.
YN250395 Fozivudine tidoxil 141790-23-0
Fozivudine tidoxil (BM-211290) is an orally active thioether lipid-zidovudine (ZDV) conjugate withanti-HIVactivity. Fozivudine tidoxil, a member of the NRTI family of drug, is incorporated into the newly synthesized str and o...
Azt-pmap, a nucleoside analogue, is an aryl phosphate derivative of AZT. Azt-pmap shows anti-HIV activity. AZT is a nucleoside reverse transcriptase inhibitor (NRTI) for HIV infection.
YYA-021 is a small-molecule CD4 mimic that inhibits HIV entry, with high anti-HIV activity and low cytotoxicity.
YN250119 Delavirdine mesylate 147221-93-0
Delavirdine Mesylate is a mesylate salt form of delavirdine, which is a synthetic, non-nucleoside reverse transcriptase inhibitor.
Loviride (R 89439) is a non-nucleoside reverse transcriptase inhibitor (NNRTI), with an IC50 of 0.3 µM forreverse transcriptasefromHIV-1. Loviride (R 89439) inhibits HIV-1, HIV-2 and SIV replication in MT-4 cell...
YN251841 HIV p17 Gag (77-85) 147468-65-3
HIV p17 Gag (77-85) is an HLA-A*0201(A2)-restricted CTL epitope, used in the research of anti-HIV.
YN250634 Trovirdine 149488-17-5
Trovirdine inhibits HIV-1 RT with an IC50 of 7nM when employing heteropolymeric primer/template (oligo-DNA/ribosomal RNA) and dGTP as substrate. Trovirdine is currently in phase I clinical trials for potential use in th...
YN250012 Emtricitabine S-oxide 152128-77-3
Emtricitabine S-oxide (Emtricitabine sulfoxide) is a major degradation product of Emtricitabine. Emtricitabine is a potent nucleoside reverse transcriptase inhibitor used for the treatment of HIV infection.
YN251799 Enfuvirtide 159519-65-0
Enfuvirtide is an anti-HIV-1fusion inhibitor peptide.
YN250613 Apricitabine 160707-69-7
Apricitabine (SPD754; AVX754), the (-) enantiomer of 2′-deoxy-3′-oxa-4′-thiocytidine (dOTC), is a highly selective and orally activeHIV-1 reverse transcriptase (RT)inhibitor (Ki=0.08μM), as well as inhibits DNA pol...
YN251629 Triptonine B 168009-85-6
Triptonine B, a sesquiterpene pyridine alkaloid that isolated fromTripterygium hypoglaucum and Tripterygium wilfordii, inhibitsHIVreplication in H9 lymphocytes with an EC50 value of <0.10 μg/mL.
YN251539 Bevirimat 174022-42-5
Bevirimat(YK FH312; FH11327; MPC-4326) is an anti-HIV drug derived from a betulinic acid-like compound
YN251724 InteriotherinA 181701-06-4
Interiotherin A is a lignan with a dibenzocyclooctadiene skeleton isolated fromKadsura interior. Interiotherin A inhibitsHIVreplication to exhibit anti-HIV activity, it has a role as a metabolite and an anti-HIV agent.
TAT (YGRKKRRQRRR) is derived from the transactivator of transcription (TAT) of human immunodeficiency virus-1 (HIV-1) and is a cell-penetrating peptide. TAT can increase the yields and the solubility of heterologo...
YN250574 Tenofovir hydrate 206184-49-8
Tenofovir (GS-1278) hydrate blocks reverse transcriptase and hepatitis B virus infections.
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