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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NBD-556
CAS:<p>NBD-556 is a small molecule mimetic of CD4. NBD-556 recognizes the HIV-1 envelope protein gp120 and induces restructuring of gp120 analogous to CD4 binding.</p>Formula:C17H24ClN3O2Purity:99.79%Color and Shape:SolidMolecular weight:337.84Islatravir
CAS:<p>Islatravir (MK-8591) is an effective anti-HIV-1 agent.</p>Formula:C12H12FN5O3Purity:98.77%Color and Shape:SolidMolecular weight:293.25TERT-IN-1
CAS:<p>TERT-IN-1 has anti-HIV activity and can be used to study HIV infection.</p>Formula:C16H20ClN3SPurity:99.31%Color and Shape:SoildMolecular weight:321.87Salicylanilide
CAS:<p>Salicylanilide (2-Hydroxybenzanilide)s are a group of compounds with antiviral potency, antibacterial and antifungal activities.</p>Formula:C13H11NO2Purity:99.55%Color and Shape:White To Off-White Crystalline PowderMolecular weight:213.23PF-3450074
CAS:<p>PF-3450074 (PF-74) is a specific HIV-1 inhibitor, blocking viral replication and uncoating at submicromolar EC50=8-640 nM.</p>Formula:C27H27N3O2Purity:99.92%Color and Shape:SolidMolecular weight:425.52Atazanavir sulfate
CAS:<p>Atazanavir sulfate, an azapeptide HIV-protease inhibitor, treats HIV/AIDS alongside other anti-HIV drugs.</p>Formula:C38H52N6O7·H2SO4Purity:99.31% - 99.40%Color and Shape:SolidMolecular weight:802.93Tenofovir diphosphate TEA
CAS:<p>Tenofovir diphosphate TEA (TFV-DP TEA) is an ATP-competitive DNA polymerase inhibitor that inhibits HIV-1 reverse transcriptase that\has anti-HIV/HBV potential.</p>Formula:C9H16N5O10P3·C6H15NPurity:93.45% - 98.51%Color and Shape:SolidMolecular weight:548.36Elsulfavirine
CAS:<p>Elsulfavirine (VM-1500) is an HIV-1 infection reverse transcriptase inhibitor. It is a new anti-HIV drug.</p>Formula:C24H17BrCl2FN3O5SPurity:99.66%Color and Shape:SolidMolecular weight:629.28BRD-6929
CAS:<p>BRD-6929, a brain-targeted HDAC1/2 inhibitor (IC50 1/8 nM), enhances gnidimacrin's anti-HIV effect, useful in mood behavior studies.</p>Formula:C19H17N3O2SPurity:98.01% - 99.05%Color and Shape:SolidMolecular weight:351.42Benfotiamine
CAS:<p>Benfotiamine (S-Benzoylthiamine O-monophosphate) is a synthetic S-acyl derivative of thiamine (vitamin B1), used as an antioxidant dietary supplement.</p>Formula:C19H23N4O6PSPurity:99.2% - 99.91%Color and Shape:Shinning Black PowderMolecular weight:466.45(S)-(+)-N-3-Benzylnirvanol
CAS:<p>(S)-(+)-N-3-Benzylnirvanol is a cytochrome P450 CYP2C19 inhibitor with a ki value of 82.5μM for CYP2C9 and 0.25μM for CYP2C19.Cost-effective and quality-assured.</p>Formula:C18H18N2O2Purity:98.90%Color and Shape:SoildMolecular weight:294.35GSK2838232
CAS:<p>GSK2838232 inhibit HIV reverse transcriptase activity across a broad panel of HIV-1 isolates,GSK2838232 is novel human immune virus (HIV) maturation inhibitor.</p>Formula:C48H73ClN2O6Purity:97.97%Color and Shape:SolidMolecular weight:809.56Pepstatin
CAS:<p>Pepstatin (Pepsin Inhibitor S 735A) is a specific and orally aspartate protease inhibitor that also inhibits HIV protease activity. Cost effective and quality assured.</p>Formula:C34H63N5O9Purity:96.74% - 99.94%Color and Shape:SolidMolecular weight:685.89Ibalizumab
CAS:<p>Ibalizumab(TMB-355) is a humanized IgG4 monoclonal antibody that acts as a CD4 receptor inhibitor, blocking the entry of HIV-1 into cells by binding to the CD4</p>Purity:SDS-PAGE:96.4%;SEC-HPLC:97.7%Color and Shape:LiquidMolecular weight:147.3 kDa3-Deazaadenosine hydrochloride
CAS:<p>3-Deazaadenosine HCl blocks SAH hydrolase (Ki: 3.9 μM), with anti-inflammatory, anti-proliferative, and anti-HIV effects.</p>Formula:C11H15ClN4O4Purity:98.48%Color and Shape:SolidMolecular weight:302.71(Rac)-Telinavir
CAS:<p>N1 compound with anti-HIV activity; contains dimethyl, phenyl, quinoline groups.</p>Formula:C33H44N6O5Purity:99.30%Color and Shape:SolidMolecular weight:604.74Probenecid
CAS:<p>Probenecid (Benemid) is a benzoic acid derivative with antihyperuricemic property.</p>Formula:C13H19NO4SPurity:98.95% - 99.84%Color and Shape:Crystals From Dil Alcohol Pleasant Aftertaste (Ntp 1992)Molecular weight:285.36Hck-IN-1
CAS:<p>Hck-IN-1 selectively inhibits Nef:Hck, IC50: 2.8 μM; >20 μM for Hck alone. Potent HIV-1 Nef antagonist, IC50: 100-300 nM for HIV-1 replication.</p>Formula:C16H11ClN6O3SPurity:99.07%Color and Shape:SolidMolecular weight:402.81Atazanavir
CAS:<p>Atazanavir (BMS-232632)(BMS-232632) is an highly effective HIV-1 protease inhibitor.</p>Formula:C38H52N6O7Purity:98% - 99.95%Color and Shape:Crystalline SolidMolecular weight:704.86Nevirapine
CAS:<p>Nevirapine (NVP) is a benzodiazepine non-nucleoside reverse transcriptase inhibitor.</p>Formula:C15H14N4OPurity:99.58% - 99.59%Color and Shape:White Or Off-White Crystalline PowderMolecular weight:266.3Dolutegravir intermediate-1
CAS:<p>Dolutegravir intermediate-1 is a synthetic precursor for HIV-1 treatment from patent WO 2016125192 A2.</p>Formula:C13H17NO8Purity:99.52%Color and Shape:SolidMolecular weight:315.28Fostemsavir Tris
CAS:<p>Fostemsavir Tris (BMS-663068 Tris) is the prodrug of BMS-626529,is a oral, safe and effective inhibitor of HIV-1 attachment.</p>Formula:C29H37N8O11PPurity:99.45%Color and Shape:SolidMolecular weight:704.62Ritonavir
CAS:<p>Ritonavir (ABT 538) inhibits HIV-1/2 proteases; serum proteins limit it but it enhances other HIV drugs by hindering P450 degradation.</p>Formula:C37H48N6O5S2Purity:99.38% - 99.96%Color and Shape:White PowderMolecular weight:720.94Zalcitabine
CAS:<p>Zalcitabine (ddC) is a nucleoside analog inhibiting HIV by blocking reverse transcriptase and halting viral DNA synthesis.</p>Formula:C9H13N3O3Purity:99.08% - ≥95%Color and Shape:White To Off-White Crystalline PowderMolecular weight:211.22Ac-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:846.93VRC01LS
<p>VRC01LS is a humanized monoclonal antibody inhibitor that targets the CD4 binding site of the HIV-1 envelope glycoprotein (Env). By blocking the interaction between HIV-1 and the host cell's CD4 receptor, VRC01LS inhibits viral entry. It holds potential for research in HIV-1 infection.</p>Color and Shape:Odour LiquidGanoderic acid GS-1
CAS:<p>Ganoderic acid GS-1, an extensively oxygenated lanostane-type triterpenoid, exhibits anti-HIV-1 protease activities, displaying an IC50 value of 58 μM [1].</p>Formula:C30H42O6Color and Shape:SolidMolecular weight:498.65Inophyllum B
CAS:<p>(+)-Inophyllum B, an HIV Reverse Transcriptase inhibitor, IC50: 38 nM; blocks HIV-1 in vitro, IC50: 1.4 μM; from Achatina fulica.</p>Formula:C25H24O5Color and Shape:SolidMolecular weight:404.46Tenofovir-C3-O-C15-CF3 ammonium
CAS:<p>Tenofovir-C3-O-C15-CF3 (ammonium) has a longer half-life and stronger anti-HIV action, improving pharmacokinetics in vivo.</p>Formula:C28H52F3N6O5PColor and Shape:SolidMolecular weight:640.73Ditiocarb
CAS:<p>Ditiocarb speeds up copper cementation, cuts HIV risk, and boosts high-risk breast cancer immunoresearch.</p>Formula:C5H11NS2Color and Shape:SolidMolecular weight:149.28GP120, 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:3002.5Pol (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:991.18Protease Inhibitor Library
<p>A unique collection of 343 protease and proteasome inhibitors for research in chemical genomics, and drug screening;</p>Color and Shape:Odour Solid[(Cys(Bzl)84,Glu(OBzl)85)]CD4 (81-92)
CAS:<p>[(Cys(Bzl)84, Glu(OBzl)85)]CD4 (81-92) is a selective HIV-1 inhibitor that blocks the interaction between HIV-1 and CD4 molecules, thereby inhibiting viral infection and cell fusion. At a concentration of 25 μM, it can completely prevent fusion formation [1].</p>Formula:C76H108N14O26SColor and Shape:SolidMolecular weight:1665.81HIV protease-IN-1
CAS:<p>HIV protease-IN-1 (compound 1·succinate), a potent non-peptidic inhibitor of HIV protease, is utilized for AIDS research [1].</p>Formula:C39H40ClF7N10O7Color and Shape:SolidMolecular weight:929.24HIV-1 integrase inhibitor 10
<p>HIV-1 integrase inhibitor 10: oral ALLINI, blocks NLRepRluc virus in MT-2 cells, EC50 of 3-5 nM, used in HIV-1 research.</p>Formula:C40H45N7O4Color and Shape:SolidMolecular weight:687.83Antitumor agent-191
<p>Antitumor agent-191 (Compound 7) exhibits antiviral activity against HSV-1 and HIV, with EC50 values of 0.03 μM and 0.81 μM, respectively. It also demonstrates potential antitumor properties by inhibiting cancer cell lines HepG2, WI-38, Vero, and MCF-7, with IC50 values of 19.6, 39.3, 18.3, and 28 μM, respectively.</p>Formula:C22H14N12S2Color and Shape:SolidMolecular weight:510.557Acetyl-pepstatin
CAS:<p>Streptomyces pepsin inhibitor is used as a pepsin inhibitor.</p>Formula:C31H57N5O9Color and Shape:SolidMolecular weight:643.81HIV Protease Substrate 1 TFA
<p>HIV Protease Substrate 1 TFA, a fluorogenic substrate for HIV protease, facilitates the investigation of the enzyme's activity [1].</p>Formula:C94H134F3N27O25SColor and Shape:SolidMolecular weight:2131.29PROTAC 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 SolidPeritassine A
CAS:<p>Peritassine A, an alkaloid derived from Tripterygium wilfordii Hook. f., exhibits anti-HIV properties.</p>Formula:C38H47NO18Color and Shape:SolidMolecular weight:805.783Morin 3-O-β-D-glucopyranoside
CAS:<p>Morin 3-O-β-D-glucopyranoside, a natural flavonoid, exhibits antifungal, anticancer, and antioxidant properties.</p>Formula:C21H20O12Color and Shape:SolidMolecular weight:464.38SDZ 283-910
CAS:<p>SDZ 283-910 is used as a statine-derived inhibitor.</p>Formula:C46H59N5O9Purity:98%Color and Shape:SolidMolecular weight:826.004N36Mut(e,g)
<p>N36Mut(e,g) is an HIV fusion peptide inhibitor targeting gp41. It functions by disrupting the formation of the homotrimeric coiled coil of the N-terminal helix in the pre-hairpin intermediate, leading to the creation of a heterotrimer.</p>Formula:C189H317N55O56Color and Shape:SolidMolecular weight:4255.87CTP518
CAS:<p>CTP518, a deuterated Atazanivir derivative, is a HIV protease inhibitor.</p>Formula:C38H52N6O7Purity:98%Color and Shape:SolidMolecular weight:719.95HIV-1 inhibitor-12
<p>HIV-1 inhibitor-12: potent at inhibiting HIV-1 capsid protein polymerization with 9 nM IC50.</p>Formula:C42H36ClF10N7O5S2Color and Shape:SolidMolecular weight:1008.35HIV-1 inhibitor-11
<p>HIV-1 inhibitor-11, a fused pyridine ring derivative, is a HIV-1 inhibitor.</p>Formula:C42H36ClF10N7O5S2Color and Shape:SolidMolecular weight:1008.35(2S,5S)-Censavudine
<p>(2S,5S)-Censavudine, a potent HIV inhibitor and nucleoside reverse transcriptase blocker.</p>Formula:C12H12N2O4Color and Shape:SolidMolecular weight:248.23HIV-1 inhibitor-6
CAS:<p>HIV-1 inhibitor-6 (3-Pyridinecarboxamide, 1,4-dihydro-1-methyl-N-(5-nitro-1,2-benzisothiazol-3-yl)-4-oxo-) is a potent HIV-1 pre-mRNA selective splicing</p>Formula:C14H10N4O4SPurity:99.33%Color and Shape:SolidMolecular weight:330.32Tenofovir-C3-O-C12-trimethylsilylacetylene ammonium
CAS:<p>Tenofovir-C3-O-C12 has a longer half-life, potent anti-HIV effects, and better pharmacokinetics than tenofovir.</p>Formula:C29H55N6O5PSiColor and Shape:SolidMolecular weight:626.855SPD-756
CAS:<p>SPD-756, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C12H16N6O3Purity:98%Color and Shape:SolidMolecular weight:292.29NNRT-IN-6
<p>NNRT-IN-6 (Compound 13a) is a non-nucleoside reverse transcriptase inhibitor (NNRT) used to inhibit HIV-1 reverse transcriptase (HIV-1RT), with an IC50 of 0.41 μM. It effectively suppresses both wild-type HIV-1 and mutants L100I, K103N, Y181C, Y188L, E138K, F227L/V106A, and RES056, with an EC50 range of 6.2-250 nM.</p>Formula:C32H31N9O3SColor and Shape:SolidMolecular weight:621.71Aureothin
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:397.42HIV-1 inhibitor-80
<p>HIV-1inhibitor-80 (compound M44) is an HIV-1 inhibitor with an EC50 of 5-148 nM. It demonstrates excellent metabolic stability and low cytotoxicity in human plasma and liver microsomes.</p>Formula:C26H19N7OColor and Shape:SolidMolecular weight:445.475Bictegravir Sodium
CAS:<p>Bictegravir Sodium is an HIV-1 integrase inhibitor with 7.5 nM IC50, offering strong, selective anti-HIV effects and minimal toxicity.</p>Formula:C21H17F3N3NaO5Purity:99.97%Color and Shape:SolidMolecular weight:471.36CI-39
CAS:<p>CI-39, an NNRTI with EC50 of 3.40 µM, inhibits HIV-1 reverse transcriptase and RNase H, with CC50 >30 µM.</p>Formula:C19H18N2O4Color and Shape:SolidMolecular weight:338.36Indoline
CAS:<p>Compound PDK0239, with CAS No. 496-15-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Compound PDK0239 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.</p>Formula:C8H9NColor and Shape:Clear To Yellow LiquidMolecular weight:119.16(-)-Rabdosiin
CAS:<p>(-)-Rabdosiin, identified as a novel phenolic marker in Symphytum officinale L., exhibits antioxidant, neuroprotective, and anti-HIV activities [1].</p>Formula:C36H30O16Color and Shape:SolidMolecular weight:718.61HIV-1 protease-IN-14
<p>HIV-1protease-IN-14 (compound 5ae) is an effective inhibitor of HIV-1protease, exhibiting Ki values of 0.28 nM and 56.9 nM against WTHIV-1PR and R41THIV-1PR, respectively. This compound also demonstrates low cytotoxicity.</p>Color and Shape:Odour SolidHIV-IN-2
CAS:<p>HIV-IN-2 (Compound 100) is a potent inhibitor of HIV, showing potential for research into HIV infection [1].</p>Formula:C34H27ClF7N9O3SColor and Shape:SolidMolecular weight:810.144-Deoxy-4α-phorbol
CAS:<p>4-Deoxy-4α-phorbol, a tetracyclic diterpene identified in E.</p>Formula:C20H28O5Color and Shape:SolidMolecular weight:348.43JE-2178
CAS:<p>JE-2178 is compound with high bioavailability .</p>Formula:C35H51N5O6SColor and Shape:SolidMolecular weight:669.87Hinnuliquinone
CAS:<p>Hinnuliquinone is an anti-HIV agent.</p>Formula:C32H30N2O4Purity:98%Color and Shape:SolidMolecular weight:506.59ICeD-2
<p>ICeD-2 triggers death in HIV-1 infected cells, requires HIV protease, inhibits DPP8/9, and stabilizes DPP9 in PBMCs.</p>Formula:C20H29N3OColor and Shape:SolidMolecular weight:327.46Elvucitabine
CAS:<p>Elvucitabine, a reverse transcriptase inhibitor, is used potentially for the treatment of HBV infection and HIV infection.</p>Formula:C9H10FN3O3Color and Shape:SolidMolecular weight:227.19Clavirolide L
<p>Clavirolide L (Compound 3), a dolabellane-type diterpenoid isolated from Clavularia viridis, demonstrates significant inhibition against HIV-1 without</p>Formula:C20H28O3Color and Shape:SolidMolecular weight:316.43RPR103611
CAS:<p>RPR103611, a betulinic acid derivative, inhibits HIV-1; IC50s: CCR5 (YU2) 80, CXCR4 (NL4-3) 0.27, dual-tropic (89.6) 0.17.</p>Formula:C46H78N2O6Color and Shape:SolidMolecular weight:755.12Decanoyl-RVKR-CMK TFA
CAS:<p>Decanoyl-RVKR-CMK (DecRVKRcmk) TFA effectively hinders the processing of over-expressed gp160 and suppresses HIV-1 replication.</p>Formula:C36H67ClF3N11O7Color and Shape:SolidMolecular weight:858.45Emtricitabine S-oxide
CAS:<p>Emtricitabine treats HIV; its degradation byproduct is Emtricitabine S-oxide.</p>Formula:C8H10FN3O4SPurity:98%Color and Shape:SolidMolecular weight:263.25(+)-Carbovir triphosphate
CAS:<p>(+)-Carbovir triphosphate, Abacavir's active metabolite, studied for HIV-1 resistance and inhibition mechanisms.</p>Formula:C11H16N5O11P3Color and Shape:SolidMolecular weight:487.19TAT peptide
<p>TAT peptide, a CPP, delivers molecules into cells by traversing membrane barriers using aa49-57 of TAT protein.</p>Formula:C65H124N34O15Purity:98%Color and Shape:SolidMolecular weight:1621.91HIV-1 protease-IN-4
<p>HIV-1 protease-IN-4, a prodrug of atazanavir, delivers 5x AUC & 67x C24 compared to atazanavir.</p>Formula:C48H69N7O11Color and Shape:SolidMolecular weight:920.1JE-2147
CAS:<p>JE-2147: a hybrid peptide with multiple amino acid types linked by peptide bonds.</p>Formula:C32H37N3O5SColor and Shape:SolidMolecular weight:575.72GLR-19
CAS:<p>GLR-19 is an anti-HIV peptide with demonstrated antiviral activity against HSV-2 [1] [2].</p>Formula:C102H194N40O20Purity:98%Color and Shape:SolidMolecular weight:2300.89HIV-1 protease-IN-10
<p>HIV-1 protease-IN-10 (Compound 2), exhibiting HIV-1 latency reversing activity (IC50: 0.22 μM), selectively binds to the PKCδ C1b domain (IC50: 0.69 μM) and</p>Formula:C23H40O5Purity:98%Color and Shape:SolidMolecular weight:396.56Alvircept sudotox
CAS:<p>Alvircept sudotox, a recombinant CD4 fused with exotoxin A from Pneumonas aeruginosa, is utilized in HIV infection research [1].</p>Color and Shape:LiquidCarbovir triphosphate
CAS:<p>Carbovir triphosphate (CBV-TP), a phosphorylated metabolite, serves as a research tool for studying human immunodeficiency virus (HIV) [1].</p>Formula:C11H16N5O11P3Color and Shape:SolidMolecular weight:487.19Kni 102
CAS:<p>Kni 102 is a biochemical.</p>Formula:C31H41N5O7Color and Shape:SolidMolecular weight:595.69Lopinavir Metabolite M-1
CAS:<p>Lopinavir Metabolite M-1, derived from Lopinavir, inhibits HIV protease (Ki=0.7 pM) and shows antiviral activity in vitro.</p>Formula:C37H46N4O6Color and Shape:SolidMolecular weight:642.78Scirpusin A
CAS:<p>Scirpusin A is a hydroxystilbene dimer from the rhizome of Scirpus fluviatilis and Xinjiang wine grape.</p>Formula:C28H22O7Color and Shape:SolidMolecular weight:470.47NF279
CAS:<p>P2X1 antagonist</p>Formula:C49H36N6Na6O23S6Purity:98%Color and Shape:SolidMolecular weight:1407.17HIV-1 inhibitor-59
<p>HIV-1 Inhibitor-59 (Compound I-5b) effectively inhibits both wild-type and mutant strains of HIV-1, with EC50 values ranging from 5.62 to 171 nM.</p>Formula:C28H28FN5O3SColor and Shape:SolidMolecular weight:533.62QYL-685
CAS:<p>QYL-685 is a methylenecyclopropane nucleoside analog.</p>Formula:C20H24N7O5PColor and Shape:SolidMolecular weight:473.42Delavirdine
CAS:<p>Delavirdine, an NNRTI for HIV-1, is used in HAART.</p>Formula:C22H28N6O3SColor and Shape:SolidMolecular weight:456.56Hypoglaunine D
CAS:<p>Hypoglaunine D, an anti-HIV analogue of Triptonine B, inhibits HIV in H9 cells with an EC50 of 22 μg/ml.</p>Formula:C41H47NO19Color and Shape:SolidMolecular weight:857.81HIV-IN-9
<p>HIV-IN-9 (Compound 2b) is an HIV inhibitor with an IC50 value of 6.65 μg/mL, demonstrating high binding affinity for HIV-RT.</p>Color and Shape:Odour SolidKadsuralignan 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:402.44MB-66
<p>MB-66 (MAPP-66) is a fully human IgG1 antibody targeting HSV and HIV. It is a monoclonal antibody membrane intended for vaginal application. The isotype control for MB-66 can be referred to as HumanIgG1kappa, Isotype Control.</p>Color and Shape:Odour LiquidCys-TAT(47-57)
CAS:<p>Cys-TAT(47-57): arginine-rich peptide from HIV-1 TAT protein's transduction domain.</p>Formula:C67H124N34O14SPurity:98%Color and Shape:SolidMolecular weight:1661.99HIV-1 inhibitor-58
<p>HIV-1 Inhibitor-58 (Compound 10c) is a non-nucleoside reverse transcriptase inhibitor with broad-spectrum antiviral properties, effective against both wild-type</p>Formula:C26H24N6O2Color and Shape:SolidMolecular weight:452.5112-Oxocalanolide A
<p>12-Oxocalanolide A is a useful organic compound for research related to life sciences and the catalog number is T125675.</p>Formula:C22H24O5Color and Shape:SolidMolecular weight:368.429Salvianan A
CAS:<p>1,6,11-Trimethyl-1,2-dihydrofuro[2',3':1,2]phenanthro[4,3-d]oxazole (compound 1) serves as an effective anti-HIV-1 agent [1].</p>Formula:C20H17NO2Color and Shape:SolidMolecular weight:303.35Amdoxovir
CAS:<p>Amdoxovir is a reverse transcriptase inhibitor.</p>Formula:C9H12N6O3Color and Shape:SolidMolecular weight:252.23HIV gag peptide (197-205)
CAS:<p>HIV gag peptide (197-205) is a H-2Kd-restricted epitope derived from the p24 portion of the HIV-1 gag protein and composed of the amino acid 197-205 (AMQMLKETI</p>Formula:C45H81N11O14S2Purity:98%Color and Shape:SolidMolecular weight:1064.32MPG, 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:2766.22Kuguacin N
<p>Kuguacin N is a useful organic compound for research related to life sciences and the catalog number is T126345.</p>Formula:C30H46O4Color and Shape:SolidMolecular weight:470.694Peptide T TFA
CAS:<p>Peptide T (TFA), an octapeptide from HIV-1 gp120, inhibits HIV binding to CD4.</p>Formula:C37H56F3N9O18Purity:98%Color and Shape:SolidMolecular weight:971.89Peptide 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:857.86HIV-1 inhibitor-81
<p>HIV-1inhibitor-81 (Compound 14g) is an HIV-1 protease inhibitor with a Ki of 1.6 nM. This compound exhibits antiviral activity against HIV-1, with an EC50 value of 250 nM.</p>Formula:C32H44N2O8SColor and Shape:SolidMolecular weight:616.77Globotriaosylceramides (porcine)
CAS:<p>Globotriaosylceramides, cell membrane glycosphingolipids, act as Shiga toxin receptors and accumulate in Fabry disease, resisting HIV by blocking gp120.</p>Formula:C60H113NO18Color and Shape:SolidMolecular weight:1136.553
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