
HIV Protease
HIV Protease inhibitors are a class of antiretroviral drugs that specifically target the protease enzyme of the Human Immunodeficiency Virus (HIV). By inhibiting this enzyme, these compounds prevent the virus from processing its polyproteins into mature, functional proteins, thereby blocking the production of new infectious virions. HIV Protease inhibitors are a cornerstone of highly active antiretroviral therapy (HAART) used to manage HIV/AIDS. At CymitQuimica, we provide a variety of HIV Protease inhibitors to support your research in HIV treatment, drug resistance, and virology.
Found 447 products of "HIV Protease"
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Aureothin
CAS:<p>Aureothin: a nitroaryl polyketide with antitumor, antifungal & insecticidal properties; inhibits NADH:oxidoreductase (IC50s: 0.07-22 nmol/mg).</p>Formula:C22H23NO6Color and Shape:SolidMolecular weight:397.42Kadsuralignan A
CAS:<p>Kadsuralignan A (compound 1), a dibenzocyclooctadiene lignan extracted from the leaves and stems of Schisandra lancifolia, exhibits anti-HIV activity, with an</p>Formula:C22H26O7Color and Shape:SolidMolecular weight:402.44GP120, HIV-1 MN
<p>GP120, HIV-1 MN, a peptide, is utilized in researching HIV infection [1] [2].</p>Formula:C135H221N45O33Color and Shape:SolidMolecular weight:3002.5Schineolignin B
<p>Schineolignin B is a useful organic compound for research related to life sciences and the catalog number is T126011.</p>Formula:C22H30O5Color and Shape:SolidMolecular weight:374.477PROTAC Vif degrader-1
<p>PROTACVif degrader-1 (Compound L15) is a Vif-targeted PROTAC degrader exhibiting anti-HIV-1 virucidal activity, with an EC50 of 33.35 μM against HIV-1IIIB.</p>Color and Shape:Odour SolidMPG, HIV related
CAS:<p>MPG: 27-amino acid peptide from HIV-1 gp41 & SV40 T antigen, delivers nucleic acids into cells efficiently.</p>Formula:C126H201N35O33SPurity:98%Color and Shape:SolidMolecular weight:2766.22Pol (476-484), HIV-1 RT Epitope
CAS:<p>Pol (476-484), HIV-1 RT Epitope is a biologically active peptide and represents the dominant HLA A*0201-restricted epitope within HIV-1 reverse transcriptase (</p>Formula:C46H78N12O12Color and Shape:SolidMolecular weight:991.18BNM-III-170
CAS:<p>BNM-III-170 is able to inhibit HIV-1 viral entry into target cells.</p>Formula:C25H26ClF7N6O6Color and Shape:SolidMolecular weight:674.96Peptide T
CAS:<p>Peptide T, an HIV-1 derived octapeptide, may inhibit gp120 binding to CD4 and cytokines, and affect VIP receptors.</p>Formula:C35H55N9O16Purity:98%Color and Shape:SolidMolecular weight:857.86Interiorin
CAS:<p>Interiorin, extracted from Kadsura heteroclita, exhibits moderate anti-HIV activity, exhibiting an EC_50 of 1.6 μg/mL [1].</p>Formula:C27H30O8Color and Shape:SolidMolecular weight:482.52Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2
CAS:<p>Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2, a peptide substrate for HIV-1 protease, is used in inhibition assays.</p>Formula:C38H58N10O12Color and Shape:SolidMolecular weight:846.93Enfuvirtide
CAS:<p>Enfuvirtide (INN) is an HIV fusion inhibitor, the first of a class of antiretroviral drugs used in combination therapy for the treatment of HIV-1 infection.</p>Formula:C204H301N51O64Purity:98%Color and Shape:White To Off-White Amorphous SolidMolecular weight:4491.945Kni 102
CAS:<p>Kni 102 is a biochemical.</p>Formula:C31H41N5O7Color and Shape:SolidMolecular weight:595.69HIV-1 inhibitor-75
<p>HIV-1inhibitor-75 is a human immunodeficiency virus 1 (HIV-1) inhibitor with an EC50 range of 0.0039-0.338 μM. Its target is the reverse transcriptase, exhibiting an IC50 value of 0.055 μM. Additionally, HIV-1inhibitor-75 demonstrates good metabolic stability in vitro, presenting moderate clearance rates and an extended half-life in human plasma and liver microsomes.</p>Formula:C25H20ClN3O3SColor and Shape:SolidMolecular weight:477.964-Acetylbutyric acid
CAS:<p>4-Acetylbutyric acid is a ketone acid widely used in biochemical experiments and drug synthesis research.</p>Formula:C6H10O3Purity:99.88%Color and Shape:SolidMolecular weight:130.14(±)-BI-D
CAS:<p>(±)-BI-D is an effective ALLINI(An allosteric IN inhibitor) that binds integrase at the LEDGF/p75 binding site (IC50: 2.4–2.9 μM).</p>Formula:C25H27NO4Color and Shape:SolidMolecular weight:405.49Abacavir hydroxyacetate
CAS:<p>Abacavir hydroxyacetate is a nucleoside analog reverse transcriptase inhibitor used in the study of HIV infection.</p>Formula:C16H20N6O3Purity:98.29%Color and Shape:SolidMolecular weight:344.37gardiquimod TFA salt
CAS:<p>Gardiquimod diTFA is a TLR7/8 agonist that may block HIV-1 in macrophages and PBMCs, active under 10 μM.</p>Formula:C21H25F6N5O5Color and Shape:SolidMolecular weight:541.44Dideoxyadenosine
CAS:<p>2',3'-Dideoxyadenosine is an inhibitor of HIV replication with antiretroviral activity and antiviral efficacy [1].</p>Formula:C10H13N5O2Purity:99.28%Color and Shape:Physical Description Off-White Powder (Ntp 1992)Molecular weight:235.242'-Deoxy-2'-fluoroarabinoadenosine
CAS:<p>2'-Deoxy-2'-fluoroarabinoadenosine is a nucleoside analogue with extensive anti-tumor activity and can be used for the study of tumor diseases.</p>Formula:C10H12FN5O3Purity:99.95%Color and Shape:SolidMolecular weight:269.23

