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Home >> Signaling Pathways >> Microbiology & Virology >> HIV

HIV

HIV (human immunodeficiency virus) is a lentivirus that infect immune system. It cause immune system failure and lead to AIDS (acquired immnudeficiency syndrome).

Products for  HIV

  1. Cat.No. Product Name Information
  2. GC18601 Stachybotrylactam Stachybotrylactam is a spirodihydrobenzofuranlactam mycotoxin originally isolated from Stachybotrys with antiviral activity. Stachybotrylactam Chemical Structure
  3. GC46020 Stachybotrysin B A fungal metabolite with antiviral and anticancer activities Stachybotrysin B Chemical Structure
  4. GC12830 Stavudine (d4T) Stavudine (d4T) (d4T) is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Stavudine (d4T) Chemical Structure
  5. GC37690 Stavudine sodium Stavudine (d4T) sodium is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Stavudine sodium Chemical Structure
  6. GC32135 TAK-220 A CCR5 antagonist TAK-220 Chemical Structure
  7. GC37724 TAK-779 An antagonist of CCR5, CXCR3, and CCR2b TAK-779 Chemical Structure
  8. GC34401 TAT TAT (YGRKKRRQRRR) is derived from the transactivator of transcription (TAT) of human immunodeficiency virus-1 (HIV-1) and is a cell-penetrating peptide. TAT Chemical Structure
  9. GC38854 TAT TFA TAT TFA (YGRKKRRQRRR) is derived from the transactivator of transcription (TAT) of human immunodeficiency virus (HIV-1) and is a cell-penetrating peptide. TAT TFA Chemical Structure
  10. GC63840 Tat-beclin 1 Tat-beclin 1, a peptide derived from a region of the autophagy protein (beclin 1), is a potent inducer of autophagy and interacts with negative regulator of autophagy, GAPR-1 (GLIPR2). Tat-beclin 1 Chemical Structure
  11. GC45004 TC 14012 (trifluoroacetate salt) C-X-C chemokine receptor type 4 (CXCR4) is a receptor for the stromal cell-derived factor-1 which is designated as chemokine ligand 12 (CXCL12). TC 14012 (trifluoroacetate salt) Chemical Structure
  12. GC12125 Tenofovir

    HIV reverse transcriptase inhibitor

     Tenofovir Chemical Structure
  13. GC37758 Tenofovir alafenamide fumarate Tenofovir alafenamide fumarate (GS-7340 fumarate) is an investigational oral prodrug of Tenofovir. Tenofovir alafenamide fumarate Chemical Structure
  14. GC37759 Tenofovir alafenamide hemifumarate Tenofovir alafenamide hemifumarate (GS-7340 hemifumarate) is an investigational oral prodrug of Tenofovir. Tenofovir alafenamide hemifumarate Chemical Structure
  15. GC45012 Tenofovir diphosphate (sodium salt) Tenofovir diphosphate is an inhibitor of HIV reverse transcriptase (Kis = 0.022 and 1.55 μM for RNA and DNA, respectively) and hepatitis B virus (HBV) polymerase (Ki = 0.18 μM). Tenofovir diphosphate (sodium salt) Chemical Structure
  16. GC37760 Tenofovir Disoproxil Tenofovir Disoproxil (Bis(POC)-PMPA) is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B. Tenofovir Disoproxil Chemical Structure
  17. GC15067 Tenofovir Disoproxil Fumarate Antiretroviral agent( HIV-1 RT inhibitor) Tenofovir Disoproxil Fumarate Chemical Structure
  18. GC13846 Tenofovir hydrate Reverse transcriptase inhibitor Tenofovir hydrate Chemical Structure
  19. GC15488 Tenofovir maleate Reverse transcriptase inhibitor Tenofovir maleate Chemical Structure
  20. GC48143 Tenofovir-d6 An internal standard for the quantification of tenofovir Tenofovir-d6 Chemical Structure
  21. GC64221 Tigloylgomisin P Tigloylgomisin P, a lignin, has anti-HIV activity with an EC50 of 37 μM. Tigloylgomisin P Chemical Structure
  22. GC14454 Tipranavir A nonpeptidic HIV protease inhibitor Tipranavir Chemical Structure
  23. GC70056 Trecovirsen

    Trecovirsen (GEM91) is an antisense oligonucleotide that targets the HIV gag gene.

     Trecovirsen Chemical Structure
  24. GC15392 Triciribine Akt inhibitor,highly selective Triciribine Chemical Structure
  25. GC41374 Trilobatin Trilobatin is a dihydrochalcone glucoside and derivative of phloretin that has been found in Rooibos (A. Trilobatin Chemical Structure
  26. GC39111 Tripterifordin Tripterifordin possesses significant anti-HIV replication activities in H9 lymphocyte cells with an EC50?value of 3100 nM, respectively. Tripterifordin Chemical Structure
  27. GC39088 Triptonine B Triptonine B, a sesquiterpene pyridine alkaloid, inhibits HIV replication in H9 lymphocytes with an EC50?value of <0.10 μg/mL. Triptonine B Chemical Structure
  28. GC32124 Trovirdine (LY300046) Trovirdine (LY300046) inhibits HIV-1 RT with an IC50 of 7 nM when employing heteropolymeric primer/template (oligo-DNA/ribosomal RNA)and dGTP as substrate. Trovirdine (LY300046) Chemical Structure
  29. GC11424 Valproic acid HDAC1 inhibitor Valproic acid Chemical Structure
  30. GC15794 Valproic acid sodium salt (Sodium valproate) A class I HDAC inhibitor Valproic acid sodium salt (Sodium valproate) Chemical Structure
  31. GC64378 Valproic acid-d6 Valproic acid-d6 (VPA-d6) is the deuterium labeled Valproic acid. Valproic acid (VPA; 2-Propylpentanoic Acid) is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2. Valproic acid activates Notch1 signaling and inhibits proliferation in small cell lung cancer (SCLC) cells. Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. Valproic acid-d6 Chemical Structure
  32. GC32110 Vesnarinone (OPC-8212) Vesnarinone (OPC-8212) (OPC-8212) is an orally active phosphodiesterase 3 (PDE3) inhibitor. Vesnarinone (OPC-8212) Chemical Structure
  33. GC17421 Vicriviroc maleate A CCR5 antagonist Vicriviroc maleate Chemical Structure
  34. GC17390 Vorinostat (SAHA, MK0683)

    An HDAC inhibitor

     Vorinostat (SAHA, MK0683) Chemical Structure
  35. GC26066 WAY-383487 WAY-383487 is one of the Tat peptide derivatives and inhibits HIV-1 long terminal repeat-activated transcription. WAY-383487 Chemical Structure
  36. GC12606 YYA-021 Competitive gp120-CD4 interaction inhibitor YYA-021 Chemical Structure
  37. GC14720 Zalcitabine Reverse transcriptase inhibitor Zalcitabine Chemical Structure
  38. GC10637 Zidovudine Reverse transcriptase inhibitor Zidovudine Chemical Structure
  39. GC37968 Zingibroside R1 A triterpene saponin and an active metabolite of ginsenoside Ro Zingibroside R1 Chemical Structure

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