
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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Atazanavir
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:704.86Atazanavir 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:802.93Hck-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:402.81Tenofovir 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:548.36(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:294.35(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:604.743-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:302.71Dolutegravir 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:315.28Salicylanilide
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:213.23Islatravir
CAS:<p>Islatravir (MK-8591) is an effective anti-HIV-1 agent.</p>Formula:C12H12FN5O3Purity:98.77%Color and Shape:SolidMolecular weight:293.25Ibalizumab
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 kDaZalcitabine
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:211.22Probenecid
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:285.36GSK2838232
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:809.56BRD-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:351.42Ritonavir
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:720.94Elsulfavirine
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:629.28Benfotiamine
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:466.45NBD-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:337.84PF-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:425.52Pepstatin
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:685.89TERT-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:321.87Fostemsavir 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:704.62Nevirapine
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:266.3AL-470
CAS:<p>AL-470 demonstrates significant antiviral efficacy, exhibiting EC50 values of 0.27 µM against HIV-1, 0.63 µM against HIV-2, and 0.35 µM against EV-A71, as</p>Formula:C67H57N7O23Color and Shape:SolidMolecular weight:1328.2Delavirdine
CAS:<p>Delavirdine, an NNRTI for HIV-1, is used in HAART.</p>Formula:C22H28N6O3SColor and Shape:SolidMolecular weight:456.56SDZ 283-910
CAS:<p>SDZ 283-910 is used as a statine-derived inhibitor.</p>Formula:C46H59N5O9Purity:98%Color and Shape:SolidMolecular weight:826.004Ditiocarb
CAS:<p>Ditiocarb speeds up copper cementation, cuts HIV risk, and boosts high-risk breast cancer immunoresearch.</p>Formula:C5H11NS2Color and Shape:SolidMolecular weight:149.28Carbovir 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:487.19HIV-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:396.56Ganoderic 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:498.65Pentosan Polysulfate
CAS:<p>Pentosan Polysulfate: anti-HIV, anti-inflammatory, supports cartilage, treats interstitial cystitis.</p>Purity:98%Color and Shape:SolidMolecular weight:N/A1-Deoxymannojirimycin hydrochloride
CAS:<p>1-Deoxymannojirimycin hydrochloride is a selective α1,2-mannosidase inhibitor(IC50: 20 μM).</p>Formula:C6H14ClNO4Purity:98%Color and Shape:SolidMolecular weight:199.63Acetyl-pepstatin
CAS:<p>Streptomyces pepsin inhibitor is used as a pepsin inhibitor.</p>Formula:C31H57N5O9Color and Shape:SolidMolecular weight:643.81Censavudine
CAS:<p>Censavudine (OBP-601) is an HIV-1/2 treatment and prevention drug, a reverse transcriptase inhibitor with EC50 of 30-890 nM.</p>Formula:C12H12N2O4Purity:98%Color and Shape:SolidMolecular weight:248.23HIV-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:1008.35RPR103611
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:755.12HIV-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 Solid(-)-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:718.61ICeD-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:327.46Decanoyl-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:858.4512-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:368.429Alvircept 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:LiquidTAT 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:1621.91Diacetylsplenopentin HCl
CAS:<p>Diacetylsplenopentin HCl, a synthetic immunomodulator, aids healthy bone marrow stem cell growth without triggering harmful immune reactions.</p>Formula:C35H56ClN9O11Purity:98%Color and Shape:SolidMolecular weight:814.33MB-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 LiquidPeritassine 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:464.38QYL-685
CAS:<p>QYL-685 is a methylenecyclopropane nucleoside analog.</p>Formula:C20H24N7O5PColor and Shape:SolidMolecular weight:473.42Pirmitegravir
CAS:<p>Pirmitegravir (STP0404) is a potent ALLINI, blocks LEDGF/p75 site, shows antiviral action against HIV.</p>Formula:C27H31ClN4O3Purity:99.79% - 99.79%Color and Shape:SolidMolecular weight:495.01Protease 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 SolidNNRT-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:621.71HIV-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:920.1Elvucitabine
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:227.19Bictegravir 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:471.36[(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:1665.81Hinnuliquinone
CAS:<p>Hinnuliquinone is an anti-HIV agent.</p>Formula:C32H30N2O4Purity:98%Color and Shape:SolidMolecular weight:506.59Clavirolide 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:316.43HIV-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 SolidClathrin-IN-1
CAS:<p>Pitstop 2 inhibits clathrin-mediated endocytosis, targeting clathrin's terminal domain, with potential in cancer research.</p>Formula:C20H13BrN2O3S2Purity:99.53%Color and Shape:SolidMolecular weight:473.36Ac-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:846.93NNRTIs-IN-3
<p>NNRTIs-IN-3 (compound 8) is an HIV-1 non-nucleoside reverse transcriptase inhibitor, displaying potent efficacy with an EC50 value of 0.01 µM [1].</p>Formula:C17H20ClN5OPurity:98%Color and Shape:SolidMolecular weight:345.83KRH-3955 Salt
CAS:<p>KRH-3955, a CXCR4 antagonist, is an orally bioavailable and extremely potent inhibitor of HIV-1 infection.</p>Formula:C40H63N7O18Purity:98%Color and Shape:SolidMolecular weight:929.96HIV 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:1064.32(2S,5S)-Censavudine
<p>(2S,5S)-Censavudine, a potent HIV inhibitor and nucleoside reverse transcriptase blocker.</p>Formula:C12H12N2O4Color and Shape:SolidMolecular weight:248.23Tenofovir-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:626.855Kni 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:477.96CI-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:338.36Tenofovir-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:640.73Pol (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:991.18N36Mut(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:4255.87Emtricitabine S-oxide
CAS:<p>Emtricitabine treats HIV; its degradation byproduct is Emtricitabine S-oxide.</p>Formula:C8H10FN3O4SPurity:98%Color and Shape:SolidMolecular weight:263.25Fluorescent HIV Substrate
CAS:<p>Fluorescent HIV Substrate is a HIV substrate.</p>Formula:C50H76N14O14Color and Shape:SolidMolecular weight:1097.22AI 3-16787
CAS:<p>AI 3-16787 is an HIV-1 integrase inhibitor exhibiting inhibitory activity against strand transfer in the presence of Mn²⁺.</p>Formula:C21H24O4Purity:99.01%Color and Shape:SolidMolecular weight:340.41CA inhibitor 1
CAS:<p>CA inhibitor 1 (GS-6207 analog) is a potent inhibitor of the HIV capsid.</p>Formula:C41H36ClF8N7O5S2Purity:98%Color and Shape:SolidMolecular weight:958.34GP120, 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:3002.5HIV-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:810.14Kadsuralignan 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:402.44HIV-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:616.77Decanoyl-RVKR-CMK
CAS:<p>Inhibits all seven proprotein convertases; stops proET-1 processing; hinders VGF secretion in PC12 cells.</p>Formula:C34H66ClN11O5Purity:98%Color and Shape:SolidMolecular weight:744.42HIV-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:533.62Lopinavir 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:642.781,6-Digalloylglucose
CAS:<p>1,6-Digalloylglucose is a useful organic compound for research related to life sciences. The catalog number is T125261 and the CAS number is 23363-08-8.</p>Formula:C20H20O14Color and Shape:SolidMolecular weight:484.366UK-88947 HCl
CAS:<p>UK 88947 is a protease inhibitor.</p>Formula:C41H63ClN6O6Purity:98%Color and Shape:SolidMolecular weight:771.44HIV-1 inhibitor-78
<p>HIV-1inhibitor-78 (compound 15f) is a potent and broad-spectrum non-nucleoside reverse transcriptase inhibitor, with an EC50 value of 3 nM against wild-type HIV-1. It is useful for research on HIV infections.</p>Formula:C32H34N6O4SColor and Shape:SolidMolecular weight:598.72BMS-955176 TFA
CAS:<p>GSK3532795: Oral HIV-1 maturation inhibitor, broad virus coverage, EC50: 15 nM, good preclinical pharmacokinetics.</p>Formula:C44H64N2O8SPurity:98%Color and Shape:SolidMolecular weight:781.06Schineolignin 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:374.477Cys-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:1661.99Aureothin
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:397.42CTP518
CAS:<p>CTP518, a deuterated Atazanivir derivative, is a HIV protease inhibitor.</p>Formula:C38H52N6O7Purity:98%Color and Shape:SolidMolecular weight:719.95(+)-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:487.194-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:130.14JE-2178
CAS:<p>JE-2178 is compound with high bioavailability .</p>Formula:C35H51N5O6SColor and Shape:SolidMolecular weight:669.87HIV 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:929.24PROTAC 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 SolidPeptide 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:971.89Pegaldesleukin
CAS:<p>Pegaldesleukin, a PEG-IL2 conjugate, exhibits antiviral properties, potentially slowing HIV progression, preserving immune function.</p>Color and Shape:LiquidInophyllum 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:404.46HIV-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:330.32HIV p17 Gag (77-85)
CAS:<p>Targeting HIV Gag p17 (77-85) with intracellular Ab cDNA disrupts viral replication pre/post-integration.</p>Formula:C44H72N10O15Purity:98%Color and Shape:SolidMolecular weight:981.1Hypoglaunine 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:857.81SPD-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:292.29Scirpusin 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:470.47HIV-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:452.51Salvianan 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:303.35Mk-6186 HCl
<p>MK-6186 HCl, a novel non-nucleoside reverse transcriptase inhibitor with antiviral activity, can be used to study HIV.</p>Formula:C21H13Cl3N6OPurity:98.19%Color and Shape:SoildMolecular weight:471.73Acetyl-binankadsurin A
CAS:<p>Acetyl-binankadsurin A (compound 5), a lignan obtained from Kadsura longipedunculata, exhibits weak inhibitory effects on HIV-1 protease, demonstrating an IC50</p>Formula:C24H28O8Purity:98%Color and Shape:SolidMolecular weight:444.47L 754394
CAS:<p>L 754394 is an effective and specific inhibitor of the HIV-1 protease.</p>Formula:C38H47N5O5Color and Shape:SolidMolecular weight:653.81Epicoccone B
CAS:<p>Epicoccone B from C. globosum has DPPH scavenging (IC50=10.8μM) and α-glucosidase inhibition (IC50=27.3μM), also anti-HIV.</p>Formula:C9H8O5Color and Shape:SolidMolecular weight:196.16gp120-α4β7 binding inhibitor 11
CAS:<p>gp120-α4β7 binding inhibitor 11 is an anti-HIV agent.</p>Formula:C26H27N3O2Purity:98.57%Color and Shape:SolidMolecular weight:413.51HIV-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:1008.35Antitumor 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:510.557Globotriaosylceramides (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:1136.553JE-2147
CAS:<p>JE-2147: a hybrid peptide with multiple amino acid types linked by peptide bonds.</p>Formula:C32H37N3O5SColor and Shape:SolidMolecular weight:575.72VRC01LS
<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 LiquidBNM-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:482.52Indoline
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:119.16Cyclotriazadisulfonamide hydrochloride
CAS:<p>Cyclotriazadisulfonamide HCl blocks HIV entry by hindering CD4 translocation into the ER.</p>Formula:C31H40ClN3O4S2Purity:98%Color and Shape:SolidMolecular weight:618.25HIV 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:2131.29NF279
CAS:<p>P2X1 antagonist</p>Formula:C49H36N6Na6O23S6Purity:98%Color and Shape:SolidMolecular weight:1407.17VIR-165
<p>VIR-165, a derivative of VIRIP (353-372 of alpha1-antitrypsin), blocks several HIV-1 strains.</p>Formula:C109H158N22O25S2Purity:98%Color and Shape:SolidMolecular weight:2240.7(Iso)-Fosdevirine
CAS:<p>(Iso)-Fosdevirine ( (Iso)-GSK2248761), a reverse transcriptase (NNRTI) inhibitor with anti-HIV activity, is used in the study of neurological diseases.</p>Formula:C20H17ClN3O3PPurity:99.93%Color and Shape:SoildMolecular weight:413.79Amdoxovir
CAS:<p>Amdoxovir is a reverse transcriptase inhibitor.</p>Formula:C9H12N6O3Color and Shape:SolidMolecular weight:252.23Kuguacin 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:470.6944-Deoxy-4α-phorbol
CAS:<p>4-Deoxy-4α-phorbol, a tetracyclic diterpene identified in E.</p>Formula:C20H28O5Color and Shape:SolidMolecular weight:348.43MPG, 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:2766.22PNU-142721
CAS:<p>PNU-142721, reverse transcriptase inhibitor, is used to treat human immunodeficiency virus (HIV) infection.</p>Formula:C13H11ClN4OSColor and Shape:SolidMolecular weight:306.77GLR-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:2300.89Enfuvirtide
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:4491.945HIV-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:445.475HIV-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:687.83Dihydroobionin B
<p>Dihydroobionin B exhibits potent (please insert the rest of the sentence for revision).</p>Formula:C21H26O5Color and Shape:SolidMolecular weight:358.43Pentosan Polysulfate Sodium (W/W 43%)
CAS:<p>Pentosan Polysulfate Sodium: anti-HIV, anti-inflammatory, aids cartilage, treats interstitial cystitis.</p>Purity:98%Color and Shape:SolidMolecular weight:N/A(±)-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:344.37Dideoxyadenosine
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:269.23Pseudothymidine
CAS:<p>Pseudothymidine is a C-nucleoside analog of thymidine.</p>Formula:C10H14N2O5Purity:98%Color and Shape:SolidMolecular weight:242.23(Z)-9-Propenyladenine
CAS:<p>(Z)-9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate.</p>Formula:C8H9N5Color and Shape:SolidMolecular weight:175.19TAT (48-57)
CAS:<p>TAT (48-57) is a cell-permeable HIV-1 Tat protein fragment, amino acids 48-57.</p>Formula:C55H109N31O12Purity:98%Color and Shape:SolidMolecular weight:1396.65Tenofovir hydrate
CAS:<p>Tenofovir hydrate (GS 1278 hydrate) is a nucleotide reverse transcriptase inhibitor with antiviral activity.</p>Formula:C9H16N5O5PPurity:99.63%Color and Shape:SolidMolecular weight:305.23Etravirine D4
CAS:<p>Etravirine is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used for the treatment of HIV. Etravirine D4 is the deuterium labeled Etravirine.</p>Formula:C20H15BrN6OPurity:98%Color and Shape:SolidMolecular weight:439.3Letrazuril
CAS:<p>Letrazuril is a compound of the anti-HIV.</p>Formula:C17H9Cl2FN4O2Color and Shape:SolidMolecular weight:391.18Cabotegravir sodium
CAS:<p>Cabotegravir sodium inhibits HIV integrase (IC50: 2.5 nM), metabolized by UGT1A1, with minimal ARV interaction.</p>Formula:C19H16F2N3NaO5Color and Shape:SolidMolecular weight:427.34PL 100
CAS:<p>PL 100 could inhibit HIV-1 protease.</p>Formula:C33H44N4O6SPurity:98%Color and Shape:SolidMolecular weight:624.799-Propenyladenine
CAS:<p>9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate.</p>Formula:C8H9N5Color and Shape:SolidMolecular weight:175.19gardiquimod 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:541.44Betulin diacetate
CAS:<p>Betulin diacetate is a bioactive chemical.</p>Formula:C34H54O4Color and Shape:SolidMolecular weight:526.8Saquinavir mesylate
CAS:<p>Saquinavir mesylate (Ro 31-8959/003) is an Inhibitor of HIV Proteaseused in antiretroviral therapy</p>Formula:C39H54N6O8SPurity:99.19%Color and Shape:White Or Pale Yellow PowderMolecular weight:766.9Ditiocarb sodium
CAS:<p>Ditiocarb sodium (Sodium diethyldithiocarbamate) (sodium diethiocarbamate) is a copper reagent, which reacts with Cu2 + solution to form a complex and improves</p>Formula:C5H10NNaS2Purity:98.04%Color and Shape:White Solid CrystallineMolecular weight:171.26Delavirdine mesylate
CAS:<p>Delavirdine mesylate (BHAP-U 90152 (mesylate)) is a non-nucleoside reverse transcriptase inhibitor (NNRTI).</p>Formula:C23H32N6O6S2Purity:99.99%Color and Shape:Light Brown SolidMolecular weight:552.67Dolutegravir sodium
CAS:<p>Dolutegravir sodium (GSK-1349572A) salt(DTG; GSK1349572) is an HIV integrase inhibitor(IC50: 2.7 nM), modest activity against raltegravir-resistant signature</p>Formula:C20H18F2N3NaO5Purity:98% - 99.46%Color and Shape:SolidMolecular weight:441.36Tenofovir alafenamide
CAS:<p>Tenofovir alafenamide (GS-7340) is a nucleotide reverse transcriptase inhibitor (NRTI) and a novel ester prodrug of the antiretroviral tenofovir.</p>Formula:C21H29N6O5PPurity:99.68% - 99.81%Color and Shape:SolidMolecular weight:476.47Amprenavir
CAS:<p>Amprenavir (KVX-478) is a synthetic derivative of hydroxyethylamine sulfonamide that selectively binds to and inhibits human immunodeficiency virus (HIV)</p>Formula:C25H35N3O6SPurity:99.60% - 99.87%Color and Shape:Off-White To Pale YellowMolecular weight:505.63Cobicistat
CAS:<p>Cobicistat (GS-9350): A carbamate, thiazole derivative, and CYP3A inhibitor used to boost anti-HIV drugs for treating HIV.</p>Formula:C40H53N7O5S2Purity:97.36% - 99.62%Color and Shape:SolidMolecular weight:776.02Escin IA
CAS:<p>Escin IA (Escin IA;Aescin IA) is a triterpene saponin isolated from horse chestnut, which inhibits HIV-1 protease with IC50 values of 35 μM.</p>Formula:C55H86O24Purity:98.97% - 99.81%Color and Shape:SolidMolecular weight:1131.26Dolutegravir
CAS:<p>Dolutegravir (GSK1349572), HIV integrase inhibitor with IC50 of 2.7 nM, partly effective against some raltegravir-resistant HIV strains.</p>Formula:C20H19F2N3O5Purity:98.97% - 99.75%Color and Shape:White To Pale Yellow SolidMolecular weight:419.38Lopinavir
CAS:<p>Lopinavir (ABT-378) is a peptidomimetic HIV protease inhibitor that retains activity against HIV protease with the Val 82 mutation.</p>Formula:C37H48N4O5Purity:98% - 99.62%Color and Shape:White Crystalline SolidMolecular weight:628.8Raltegravir sodium
CAS:<p>Raltegravir (MK 0518) sodium is a potent, orally active HIV integrase (IN) inhibitor.</p>Formula:C20H20FN6NaO5Color and Shape:SolidMolecular weight:466.405Doravirine
CAS:<p>Doravirine (MK-1439) is a non-nucleoside reverse transcriptase inhibitor, used in the treatment of HIV/AIDS.</p>Formula:C17H11ClF3N5O3Purity:99.65% - 99.79%Color and Shape:SolidMolecular weight:425.75Ganoderic acid B
CAS:<p>Ganoderic acid B: quality marker for G. lucidum products, inhibits telomerase & EBV activation, moderates HIV-1 protease.</p>Formula:C30H44O7Purity:99.09% - 99.95%Color and Shape:SolidMolecular weight:516.67Didanosine
CAS:<p>Didanosine (ddI) is a nucleoside reverse transcriptase inhibitor analog of adenosine (IC50: 0.49 μM).</p>Formula:C10H12N4O3Purity:99.64%Color and Shape:White Crystalline PowderMolecular weight:236.23Temsavir
CAS:<p>Temsavir (BMS626529) is a novel attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T cells.</p>Formula:C24H23N7O4Purity:99.14%Color and Shape:SolidMolecular weight:473.48Darunavir
CAS:<p>Darunavir (TMC114) is an HIV PROTEASE INHIBITOR that is used in the treatment of AIDS and HIV INFECTIONS.</p>Formula:C27H37N3O7SPurity:99.67% - 99.76%Color and Shape:White Amorphous SolidMolecular weight:547.66BMS-707035
CAS:<p>BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.</p>Formula:C17H19FN4O5SPurity:99.78%Color and Shape:SolidMolecular weight:410.42Raltegravir
CAS:<p>Raltegravir (MK-0518) is a pyrrolidinone derivative and HIV INTEGRASE INHIBITOR that is used in combination with other ANTI-HIV AGENTS for the treatment of HIV</p>Formula:C20H21FN6O5Purity:99.86% - >99.99%Color and Shape:SolidMolecular weight:444.42TAT
CAS:<p>TAT peptide (YGRKKRRQRRR), originating from the human immunodeficiency virus-1 (HIV-1) transactivator of transcription (TAT), enhances the solubility and</p>Formula:C64H118N32O14Purity:>99.99%Color and Shape:SolidMolecular weight:1559.83Amylmetacresol
CAS:<p>Amylmetacresol treats sore throat, pharyngitis, tonsillitis, laryngitis, influenza A, and SARS-CoV.</p>Formula:C12H18OPurity:99.66%Color and Shape:SolidMolecular weight:178.27Elvitegravir
CAS:<p>Elvitegravir (JTK-303) is an HIV integrase inhibitor and CYP2C9 inducer.</p>Formula:C23H23ClFNO5Purity:98.43% - 99.57%Color and Shape:SolidMolecular weight:447.88Vesnarinone
CAS:<p>Vesnarinone (Arkin) (INN) is a mixed phosphodiesterase 3 inhibitor and ion-channel modifier that has modest, dose-dependent, positive inotropic activity, but</p>Formula:C22H25N3O4Purity:96.69% - 98.13%Color and Shape:SolidMolecular weight:395.45I-XW-053 sodium
CAS:<p>I-XW-053 sodium inhibits the replication of a diverse panel of primary HIV-1 isolates in Peripheral blood mononuclear cell with no appreciable cytotoxicity.</p>Formula:C22H16N2NaO2Color and Shape:SolidMolecular weight:363.3722,4-Dihydroxypyridine
CAS:<p>2,4-Dihydroxypyridine: a pyridine derivative, chelates metals, assesses ion levels, measures enzymatic reactions, and quantifies biomolecules.</p>Formula:C5H5NO2Purity:97.79%Color and Shape:White To Yellow-Beige Crystals OrMolecular weight:111.1PTACH
CAS:<p>PTACH (Cpd 51) (NCH-51) is a SAHA-based inhibitor of human HDAC. It can potently inhibit the growth of various human Y cells (EC50: 1 to 10 μM).</p>Formula:C20H26N2O2S2Purity:87.44% - 99.74%Color and Shape:SolidMolecular weight:390.56Darunavir Ethanolate
CAS:<p>Darunavir Ethanolate (UIC 94017) is an HIV PROTEASE INHIBITOR that is used in the treatment of AIDS and HIV INFECTIONS.</p>Formula:C29H43N3O8SPurity:99.84% - 99.86%Color and Shape:SolidMolecular weight:593.74LDC4297 hydrochloride
CAS:<p>LDC4297 hydrochloride is a selective and potent CDK7 inhibitor with broad-spectrum antiviral activity, useful for research on viral infections.</p>Formula:C23H29ClN8OColor and Shape:SolidMolecular weight:468.98Thiamine disulfide
CAS:<p>Thiamine disulfide (Algoneurina) , also known as thiamin or vitamin B1, is a vitamin found in food and manufactured as a dietary supplement and medication.</p>Formula:C24H34N8O4S2Purity:99.81%Color and Shape:CoaMolecular weight:562.71Inosine pranobex
CAS:<p>Inosine pranobex (Delimmun) has a lot of immunomodulatory effects, including inducing T-lymphocyte differentiation, augmenting macrophage and NK cell functions.</p>Formula:C52H78N10O17Purity:99.78% - 99.91%Color and Shape:SolidMolecular weight:1115.23Raltegravir potassium
CAS:<p>Raltegravir potassium (MK 0518 potassium salt) salt(MK0518 potassium salt) is a potent integrase (IN) inhibitor, used to treat HIV infection.</p>Formula:C20H20FN6O5·KPurity:98% - 99.55%Color and Shape:Off-White SolidMolecular weight:482.51Tenofovir alafenamide hemifumarate
CAS:<p>Tenofovir alafenamide hemifumarate (GS-7340 hemifumarate) is an oral phosphonoamidate prodrug of the HIV reverse transcriptase nucleotide inhibitor tenofovir.</p>Formula:C21H29N6O5PC4H4O4Purity:99.33% - 99.96%Color and Shape:SolidMolecular weight:534.51Rolipram
CAS:<p>Rolipram (SB 95952) is a phosphodiesterase 4 inhibitor with antidepressant properties.</p>Formula:C16H21NO3Purity:99.22% - >99.99%Color and Shape:SolidMolecular weight:275.34PMEDAP
CAS:<p>PMEDAP is a potent inhibitor of Moloney murine sarcoma virus (MSV)-induced tumor formation and associated mortality and an inhibitor of human immunodeficiency</p>Formula:C8H13N6O4PPurity:99.77%Color and Shape:SolidMolecular weight:288.2Dimercaprol
CAS:<p>Dimercaprol (Dicaptol) is an anti-gas warfare agent that is effective against Lewisite (dichloro(2-chlorovinyl)arsine) and formerly known as British Anti-</p>Formula:C3H8OS2Purity:98.91% - 99.64%Color and Shape:Viscous Oily LiquidMolecular weight:124.22Peldesine dihydrochloride
CAS:<p>Peldesine (BCX 34) dihydrochloride is an inhibitor of PNP in humans, rats, and mice, also hindering T-cell proliferation, used in lymphoma and HIV research.</p>Formula:C12H13Cl2N5OColor and Shape:SolidMolecular weight:314.17IMB-301
CAS:<p>IMB-301 is a small molecular inhibitor via virtual screening according to the hA3G model.</p>Formula:C19H17Cl2FN2OPurity:99.72%Color and Shape:SolidMolecular weight:379.26Fostemsavir
CAS:<p>Fostemsavir (BMS-663068) is an HIV-1 attachment inhibitor in development for the treatment of HIV-1 infection.</p>Formula:C25H26N7O8PPurity:98.95%Color and Shape:SolidMolecular weight:583.49HODHBt
CAS:<p>HODHBt is a STAT5-SUMO protein-protein interaction inhibitor.</p>Formula:C7H5N3O2Purity:99.45% - 99.95%Color and Shape:Off-White To Yellow SolidMolecular weight:163.13Rilpivirine
CAS:<p>Rilpivirine (R278474) is a diarylpyrimidine derivative and reverse transcriptase inhibitor with antiviral activity against HIV-1 that is used in the treatment</p>Formula:C22H18N6Purity:97.22% - 98.83%Color and Shape:SolidMolecular weight:366.42NBD-557
CAS:<p>NBD-557 is a potentially HIV-1 inhibitor.</p>Formula:C17H24BrN3O2Purity:99.52%Color and Shape:SolidMolecular weight:382.3Des(benzylpyridyl) Atazanavi
CAS:<p>The N-dealkylated metabolite (M1) of Atazanavir, a HIV protease inhibitor.</p>Formula:C26H43N5O7Purity:98% - 99.75%Color and Shape:SolidMolecular weight:537.65Saquinavir
CAS:<p>Saquinavir (Ro 31-8959) is a potent HIV protease inhibitor, is an antiretroviral drug used together with other medications to treat or prevent HIV/AIDS.</p>Formula:C38H50N6O5Purity:99.50% - >99.99%Color and Shape:SolidMolecular weight:670.84Dexelvucitabine
CAS:<p>Dexelvucitabine (RVT), a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C9H10FN3O3Purity:98.25%Color and Shape:SolidMolecular weight:227.19HIV-1 Nef-IN-1
CAS:<p>HIV-1 Nef-IN-1 is an inhibitor of HIV-1 Nef protein. It efficiently competes for Nef-SH3Hck interactions(Kd : 6.7 μM).</p>Formula:C18H16O2Purity:99.90%Color and Shape:SolidMolecular weight:264.32Etravirine
CAS:<p>Etravirine (R165335) is a diarylpyrimidine non-nucleoside reverse transcriptase inhibitor.</p>Formula:C20H15BrN6OPurity:97.61% - 99.74%Color and Shape:White To Off-White SolidMolecular weight:435.284-Chloro-2-(trifluoroacetyl)aniline hydrochloride
CAS:<p>4-Chloro-2-(trifluoroacetyl)aniline hydrochloride is an inhibitor of HIV-1 RT (HIV reverse transcriptase) .</p>Formula:C8H6Cl2F3NOPurity:97.15%Color and Shape:SolidMolecular weight:260.04Obefazimod
CAS:<p>Obefazimod (ABX-464) is a potent anti-HIV agent. ABX464 inhibits HIV-1 replication in stimulated peripheral blood mononuclear cells (PBMCs).</p>Formula:C16H10ClF3N2OPurity:99.86%Color and Shape:SolidMolecular weight:338.71RN-18
CAS:<p>RN-18 is an inhibitor of HIV-1 viral infectivity factor (IC50: 6 μM in nonpermissive H9 cells).</p>Formula:C20H16N2O4SPurity:97.21% - 98.39%Color and Shape:SolidMolecular weight:380.42Filgotinib
CAS:<p>Filgotinib (GLPG0634) is a selective JAK1 inhibitor. The IC50 values against JAK1, JAK2, JAK3, and TYK2 are 10 nM, 28 nM, 810 nM, and 116 nM, respectively.</p>Formula:C21H23N5O3SPurity:98.03% - ≥95%Color and Shape:SolidMolecular weight:425.5

