HIV Protease
Os inibidores da protease do HIV são uma classe de medicamentos antirretrovirais que têm como alvo específico a enzima protease do vírus da imunodeficiência humana (HIV). Ao inibir esta enzima, esses compostos impedem o vírus de processar suas poliproteínas em proteínas maduras e funcionais, bloqueando assim a produção de novos virions infecciosos. Os inibidores da protease do HIV são um pilar da terapia antirretroviral altamente ativa (HAART) utilizada para o tratamento do HIV/AIDS. Na CymitQuimica, oferecemos uma variedade de inibidores da protease do HIV para apoiar sua pesquisa em tratamento do HIV, resistência a medicamentos e virologia.
Foram encontrados 494 produtos de "HIV Protease"
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Atazanavir sulfate
CAS:Atazanavir sulfate, an azapeptide HIV-protease inhibitor, treats HIV/AIDS alongside other anti-HIV drugs.Fórmula:C38H52N6O7·H2SO4Pureza:99.31% - 99.40%Cor e Forma:SolidPeso molecular:802.93Islatravir
CAS:Islatravir (MK-8591) is an effective anti-HIV-1 agent.Fórmula:C12H12FN5O3Pureza:98.77%Cor e Forma:SolidPeso molecular:293.25NBD-556
CAS: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.Fórmula:C17H24ClN3O2Pureza:99.79%Cor e Forma:SolidPeso molecular:337.84Atazanavir
CAS:<p>Atazanavir (BMS-232632)(BMS-232632) is an highly effective HIV-1 protease inhibitor.</p>Fórmula:C38H52N6O7Pureza:98% - 99.95%Cor e Forma:Crystalline SolidPeso molecular:704.86Pepstatin
CAS:Pepstatin (Pepsin Inhibitor S 735A) is a specific and orally aspartate protease inhibitor that also inhibits HIV protease activity. Cost effective and quality assured.Fórmula:C34H63N5O9Pureza:96.74% - 99.94%Cor e Forma:SolidPeso molecular:685.89Probenecid
CAS:<p>Probenecid (Benemid) is a benzoic acid derivative with antihyperuricemic property.</p>Fórmula:C13H19NO4SPureza:98.95% - 99.84%Cor e Forma:Crystals From Dil Alcohol Pleasant Aftertaste (Ntp 1992)Peso molecular:285.36TERT-IN-1
CAS:TERT-IN-1 has anti-HIV activity and can be used to study HIV infection.Fórmula:C16H20ClN3SPureza:99.31%Cor e Forma:SoildPeso molecular:321.87Ritonavir
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>Fórmula:C37H48N6O5S2Pureza:99.38% - 99.96%Cor e Forma:White PowderPeso molecular:720.94Dolutegravir intermediate-1
CAS:Dolutegravir intermediate-1 is a synthetic precursor for HIV-1 treatment from patent WO 2016125192 A2.Fórmula:C13H17NO8Pureza:99.52%Cor e Forma:SolidPeso molecular:315.28Salicylanilide
CAS:<p>Salicylanilide (2-Hydroxybenzanilide)s are a group of compounds with antiviral potency, antibacterial and antifungal activities.</p>Fórmula:C13H11NO2Pureza:99.55%Cor e Forma:White To Off-White Crystalline PowderPeso molecular:213.23Zalcitabine
CAS:<p>Zalcitabine (ddC) is a nucleoside analog inhibiting HIV by blocking reverse transcriptase and halting viral DNA synthesis.</p>Fórmula:C9H13N3O3Pureza:99.08% - ≥95%Cor e Forma:White To Off-White Crystalline PowderPeso molecular:211.22Ibalizumab
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>Pureza:SDS-PAGE:96.4%;SEC-HPLC:97.7%Cor e Forma:LiquidPeso molecular:147.3 kDaPF-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>Fórmula:C27H27N3O2Pureza:99.92%Cor e Forma:SolidPeso molecular:425.52GSK2838232
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>Fórmula:C48H73ClN2O6Pureza:97.97%Cor e Forma:SolidPeso molecular:809.563-Deazaadenosine hydrochloride
CAS:3-Deazaadenosine HCl blocks SAH hydrolase (Ki: 3.9 μM), with anti-inflammatory, anti-proliferative, and anti-HIV effects.Fórmula:C11H15ClN4O4Pureza:98.48%Cor e Forma:SolidPeso molecular:302.71(Rac)-Telinavir
CAS:<p>N1 compound with anti-HIV activity; contains dimethyl, phenyl, quinoline groups.</p>Fórmula:C33H44N6O5Pureza:99.30%Cor e Forma:SolidPeso molecular:604.74(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>Fórmula:C18H18N2O2Pureza:98.90%Cor e Forma:SoildPeso molecular:294.35Elsulfavirine
CAS:Elsulfavirine (VM-1500) is an HIV-1 infection reverse transcriptase inhibitor. It is a new anti-HIV drug.Fórmula:C24H17BrCl2FN3O5SPureza:99.66%Cor e Forma:SolidPeso molecular:629.28Benfotiamine
CAS:Benfotiamine (S-Benzoylthiamine O-monophosphate) is a synthetic S-acyl derivative of thiamine (vitamin B1), used as an antioxidant dietary supplement.Fórmula:C19H23N4O6PSPureza:99.2% - 99.91%Cor e Forma:Shinning Black PowderPeso molecular:466.45Fostemsavir Tris
CAS:Fostemsavir Tris (BMS-663068 Tris) is the prodrug of BMS-626529,is a oral, safe and effective inhibitor of HIV-1 attachment.Fórmula:C29H37N8O11PPureza:99.45%Cor e Forma:SolidPeso molecular:704.62BRD-6929
CAS:BRD-6929, a brain-targeted HDAC1/2 inhibitor (IC50 1/8 nM), enhances gnidimacrin's anti-HIV effect, useful in mood behavior studies.Fórmula:C19H17N3O2SPureza:98.01% - 99.05%Cor e Forma:SolidPeso molecular:351.42Nevirapine
CAS:<p>Nevirapine (NVP) is a benzodiazepine non-nucleoside reverse transcriptase inhibitor.</p>Fórmula:C15H14N4OPureza:99.58% - 99.59%Cor e Forma:White Or Off-White Crystalline PowderPeso molecular:266.3Inophyllum B
CAS:(+)-Inophyllum B, an HIV Reverse Transcriptase inhibitor, IC50: 38 nM; blocks HIV-1 in vitro, IC50: 1.4 μM; from Achatina fulica.Fórmula:C25H24O5Cor e Forma:SolidPeso molecular:404.46VRC01LS
<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>Cor e Forma:Odour LiquidClathrin-IN-1
CAS:<p>Pitstop 2 inhibits clathrin-mediated endocytosis, targeting clathrin's terminal domain, with potential in cancer research.</p>Fórmula:C20H13BrN2O3S2Pureza:99.53%Cor e Forma:SolidPeso molecular:473.36Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2
CAS:Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2, a peptide substrate for HIV-1 protease, is used in inhibition assays.Fórmula:C38H58N10O12Cor e Forma:SolidPeso molecular:846.93(-)-Rabdosiin
CAS:(-)-Rabdosiin, identified as a novel phenolic marker in Symphytum officinale L., exhibits antioxidant, neuroprotective, and anti-HIV activities [1].Fórmula:C36H30O16Cor e Forma:SolidPeso molecular:718.61Tenofovir-C3-O-C12-trimethylsilylacetylene ammonium
CAS:Tenofovir-C3-O-C12 has a longer half-life, potent anti-HIV effects, and better pharmacokinetics than tenofovir.Fórmula:C29H55N6O5PSiCor e Forma:SolidPeso molecular:626.855Ditiocarb
CAS:Ditiocarb speeds up copper cementation, cuts HIV risk, and boosts high-risk breast cancer immunoresearch.Fórmula:C5H11NS2Cor e Forma:SolidPeso molecular:149.28Ganoderic 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>Fórmula:C30H42O6Cor e Forma:SolidPeso molecular:498.65Acetyl-pepstatin
CAS:<p>Streptomyces pepsin inhibitor is used as a pepsin inhibitor.</p>Fórmula:C31H57N5O9Cor e Forma:SolidPeso molecular:643.81GP120, HIV-1 MN
GP120, HIV-1 MN, a peptide, is utilized in researching HIV infection [1] [2].Fórmula:C135H221N45O33Cor e Forma:SolidPeso molecular:3002.5Peptide T
CAS:Peptide T, an HIV-1 derived octapeptide, may inhibit gp120 binding to CD4 and cytokines, and affect VIP receptors.Fórmula:C35H55N9O16Pureza:98%Cor e Forma:SolidPeso molecular:857.86HIV protease-IN-1
CAS:HIV protease-IN-1 (compound 1·succinate), a potent non-peptidic inhibitor of HIV protease, is utilized for AIDS research [1].Fórmula:C39H40ClF7N10O7Cor e Forma:SolidPeso molecular:929.24Antitumor 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>Fórmula:C22H14N12S2Cor e Forma:SolidPeso molecular:510.557HIV Protease Substrate 1 TFA
HIV Protease Substrate 1 TFA, a fluorogenic substrate for HIV protease, facilitates the investigation of the enzyme's activity [1].Fórmula:C94H134F3N27O25SCor e Forma:SolidPeso molecular:2131.29AI 3-16787
CAS:AI 3-16787 is an HIV-1 integrase inhibitor exhibiting inhibitory activity against strand transfer in the presence of Mn²⁺.Fórmula:C21H24O4Pureza:99.01%Cor e Forma:SolidPeso molecular:340.41SDZ 283-910
CAS:SDZ 283-910 is used as a statine-derived inhibitor.Fórmula:C46H59N5O9Pureza:98%Cor e Forma:SolidPeso molecular:826.004Morin 3-O-β-D-glucopyranoside
CAS:Morin 3-O-β-D-glucopyranoside, a natural flavonoid, exhibits antifungal, anticancer, and antioxidant properties.Fórmula:C21H20O12Cor e Forma:SolidPeso molecular:464.38Fluorescent HIV Substrate
CAS:<p>Fluorescent HIV Substrate is a HIV substrate.</p>Fórmula:C50H76N14O14Cor e Forma:SolidPeso molecular:1097.22Aureothin
CAS:<p>Aureothin: a nitroaryl polyketide with antitumor, antifungal & insecticidal properties; inhibits NADH:oxidoreductase (IC50s: 0.07-22 nmol/mg).</p>Fórmula:C22H23NO6Cor e Forma:SolidPeso molecular:397.42Hinnuliquinone
CAS:Hinnuliquinone is an anti-HIV agent.Fórmula:C32H30N2O4Pureza:98%Cor e Forma:SolidPeso molecular:506.59CTP518
CAS:CTP518, a deuterated Atazanivir derivative, is a HIV protease inhibitor.Fórmula:C38H52N6O7Pureza:98%Cor e Forma:SolidPeso molecular:719.95HIV-1 inhibitor-58
HIV-1 Inhibitor-58 (Compound 10c) is a non-nucleoside reverse transcriptase inhibitor with broad-spectrum antiviral properties, effective against both wild-typeFórmula:C26H24N6O2Cor e Forma:SolidPeso molecular:452.51Amdoxovir
CAS:Amdoxovir is a reverse transcriptase inhibitor.Fórmula:C9H12N6O3Cor e Forma:SolidPeso molecular:252.23HIV-1 inhibitor-12
HIV-1 inhibitor-12: potent at inhibiting HIV-1 capsid protein polymerization with 9 nM IC50.Fórmula:C42H36ClF10N7O5S2Cor e Forma:SolidPeso molecular:1008.35VIR-165
VIR-165, a derivative of VIRIP (353-372 of alpha1-antitrypsin), blocks several HIV-1 strains.Fórmula:C109H158N22O25S2Pureza:98%Cor e Forma:SolidPeso molecular:2240.7HIV-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>Fórmula:C26H19N7OCor e Forma:SolidPeso molecular:445.475HIV-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>Fórmula:C14H10N4O4SPureza:99.33%Cor e Forma:SolidPeso molecular:330.32SPD-756
CAS:<p>SPD-756, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C12H16N6O3Pureza:98%Cor e Forma:SolidPeso molecular:292.29NNRT-IN-6
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.Fórmula:C32H31N9O3SCor e Forma:SolidPeso molecular:621.71Protease Inhibitor Library
A unique collection of 343 protease and proteasome inhibitors for research in chemical genomics, and drug screening;Cor e Forma:Odour SolidRPR103611
CAS:RPR103611, a betulinic acid derivative, inhibits HIV-1; IC50s: CCR5 (YU2) 80, CXCR4 (NL4-3) 0.27, dual-tropic (89.6) 0.17.Fórmula:C46H78N2O6Cor e Forma:SolidPeso molecular:755.12HIV-1 integrase inhibitor 10
HIV-1 integrase inhibitor 10: oral ALLINI, blocks NLRepRluc virus in MT-2 cells, EC50 of 3-5 nM, used in HIV-1 research.Fórmula:C40H45N7O4Cor e Forma:SolidPeso molecular:687.83Bictegravir Sodium
CAS:Bictegravir Sodium is an HIV-1 integrase inhibitor with 7.5 nM IC50, offering strong, selective anti-HIV effects and minimal toxicity.Fórmula:C21H17F3N3NaO5Pureza:99.97%Cor e Forma:SolidPeso molecular:471.36HIV-IN-2
CAS:HIV-IN-2 (Compound 100) is a potent inhibitor of HIV, showing potential for research into HIV infection [1].Fórmula:C34H27ClF7N9O3SCor e Forma:SolidPeso molecular:810.14CI-39
CAS:CI-39, an NNRTI with EC50 of 3.40 µM, inhibits HIV-1 reverse transcriptase and RNase H, with CC50 >30 µM.Fórmula:C19H18N2O4Cor e Forma:SolidPeso molecular:338.36(2S,5S)-Censavudine
(2S,5S)-Censavudine, a potent HIV inhibitor and nucleoside reverse transcriptase blocker.Fórmula:C12H12N2O4Cor e Forma:SolidPeso molecular:248.23HIV-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>Cor e Forma:Odour Solid4-Deoxy-4α-phorbol
CAS:4-Deoxy-4α-phorbol, a tetracyclic diterpene identified in E.Fórmula:C20H28O5Cor e Forma:SolidPeso molecular:348.43JE-2178
CAS:JE-2178 is compound with high bioavailability .Fórmula:C35H51N5O6SCor e Forma:SolidPeso molecular:669.87Tenofovir-C3-O-C15-CF3 ammonium
CAS:Tenofovir-C3-O-C15-CF3 (ammonium) has a longer half-life and stronger anti-HIV action, improving pharmacokinetics in vivo.Fórmula:C28H52F3N6O5PCor e Forma:SolidPeso molecular:640.73Decanoyl-RVKR-CMK
CAS:<p>Inhibits all seven proprotein convertases; stops proET-1 processing; hinders VGF secretion in PC12 cells.</p>Fórmula:C34H66ClN11O5Pureza:98%Cor e Forma:SolidPeso molecular:744.42Clavirolide L
<p>Clavirolide L (Compound 3), a dolabellane-type diterpenoid isolated from Clavularia viridis, demonstrates significant inhibition against HIV-1 without</p>Fórmula:C20H28O3Cor e Forma:SolidPeso molecular:316.43Elvucitabine
CAS:<p>Elvucitabine, a reverse transcriptase inhibitor, is used potentially for the treatment of HBV infection and HIV infection.</p>Fórmula:C9H10FN3O3Cor e Forma:SolidPeso molecular:227.19Emtricitabine S-oxide
CAS:Emtricitabine treats HIV; its degradation byproduct is Emtricitabine S-oxide.Fórmula:C8H10FN3O4SPureza:98%Cor e Forma:SolidPeso molecular:263.25Pol (476-484), HIV-1 RT Epitope
CAS: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 (Fórmula:C46H78N12O12Cor e Forma:SolidPeso molecular:991.18Dihydroobionin B
Dihydroobionin B exhibits potent (please insert the rest of the sentence for revision).Fórmula:C21H26O5Cor e Forma:SolidPeso molecular:358.43QYL-685
CAS:QYL-685 is a methylenecyclopropane nucleoside analog.Fórmula:C20H24N7O5PCor e Forma:SolidPeso molecular:473.42Decanoyl-RVKR-CMK TFA
CAS:<p>Decanoyl-RVKR-CMK (DecRVKRcmk) TFA effectively hinders the processing of over-expressed gp160 and suppresses HIV-1 replication.</p>Fórmula:C36H67ClF3N11O7Cor e Forma:SolidPeso molecular:858.45HIV-1 protease-IN-4
HIV-1 protease-IN-4, a prodrug of atazanavir, delivers 5x AUC & 67x C24 compared to atazanavir.Fórmula:C48H69N7O11Cor e Forma:SolidPeso molecular:920.1Peritassine A
CAS:Peritassine A, an alkaloid derived from Tripterygium wilfordii Hook. f., exhibits anti-HIV properties.Fórmula:C38H47NO18Cor e Forma:SolidPeso molecular:805.783GLR-19
CAS:GLR-19 is an anti-HIV peptide with demonstrated antiviral activity against HSV-2 [1] [2].Fórmula:C102H194N40O20Pureza:98%Cor e Forma:SolidPeso molecular:2300.89(+)-Carbovir triphosphate
CAS:(+)-Carbovir triphosphate, Abacavir's active metabolite, studied for HIV-1 resistance and inhibition mechanisms.Fórmula:C11H16N5O11P3Cor e Forma:SolidPeso molecular:487.19Carbovir triphosphate
CAS:Carbovir triphosphate (CBV-TP), a phosphorylated metabolite, serves as a research tool for studying human immunodeficiency virus (HIV) [1].Fórmula:C11H16N5O11P3Cor e Forma:SolidPeso molecular:487.19TAT peptide
TAT peptide, a CPP, delivers molecules into cells by traversing membrane barriers using aa49-57 of TAT protein.Fórmula:C65H124N34O15Pureza:98%Cor e Forma:SolidPeso molecular:1621.91Kadsuralignan A
CAS:Kadsuralignan A (compound 1), a dibenzocyclooctadiene lignan extracted from the leaves and stems of Schisandra lancifolia, exhibits anti-HIV activity, with anFórmula:C22H26O7Cor e Forma:SolidPeso molecular:402.44Hypoglaunine D
CAS:Hypoglaunine D, an anti-HIV analogue of Triptonine B, inhibits HIV in H9 cells with an EC50 of 22 μg/ml.Fórmula:C41H47NO19Cor e Forma:SolidPeso molecular:857.81HIV-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>Fórmula:C28H28FN5O3SCor e Forma:SolidPeso molecular:533.62JE-2147
CAS:JE-2147: a hybrid peptide with multiple amino acid types linked by peptide bonds.Fórmula:C32H37N3O5SCor e Forma:SolidPeso molecular:575.72Scirpusin A
CAS:Scirpusin A is a hydroxystilbene dimer from the rhizome of Scirpus fluviatilis and Xinjiang wine grape.Fórmula:C28H22O7Cor e Forma:SolidPeso molecular:470.47PROTAC Vif degrader-1
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.Cor e Forma:Odour SolidDelavirdine
CAS:<p>Delavirdine, an NNRTI for HIV-1, is used in HAART.</p>Fórmula:C22H28N6O3SCor e Forma:SolidPeso molecular:456.56MB-66
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.Cor e Forma:Odour LiquidHIV-IN-9
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.Cor e Forma:Odour SolidGlobotriaosylceramides (porcine)
CAS:Globotriaosylceramides, cell membrane glycosphingolipids, act as Shiga toxin receptors and accumulate in Fabry disease, resisting HIV by blocking gp120.Fórmula:C60H113NO18Cor e Forma:SolidPeso molecular:1136.553ICeD-2
<p>ICeD-2 triggers death in HIV-1 infected cells, requires HIV protease, inhibits DPP8/9, and stabilizes DPP9 in PBMCs.</p>Fórmula:C20H29N3OCor e Forma:SolidPeso molecular:327.4612-Oxocalanolide A
12-Oxocalanolide A is a useful organic compound for research related to life sciences and the catalog number is T125675.Fórmula:C22H24O5Cor e Forma:SolidPeso molecular:368.429Cys-TAT(47-57)
CAS:Cys-TAT(47-57): arginine-rich peptide from HIV-1 TAT protein's transduction domain.Fórmula:C67H124N34O14SPureza:98%Cor e Forma:SolidPeso molecular:1661.99Salvianan 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>Fórmula:C20H17NO2Cor e Forma:SolidPeso molecular:303.35HIV gag peptide (197-205)
CAS: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 (AMQMLKETIFórmula:C45H81N11O14S2Pureza:98%Cor e Forma:SolidPeso molecular:1064.32HIV-1 inhibitor-11
HIV-1 inhibitor-11, a fused pyridine ring derivative, is a HIV-1 inhibitor.Fórmula:C42H36ClF10N7O5S2Cor e Forma:SolidPeso molecular:1008.35Kuguacin N
Kuguacin N is a useful organic compound for research related to life sciences and the catalog number is T126345.Fórmula:C30H46O4Cor e Forma:SolidPeso molecular:470.694HIV-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>Fórmula:C23H40O5Pureza:98%Cor e Forma:SolidPeso molecular:396.56Indoline
CAS: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.Fórmula:C8H9NCor e Forma:Clear To Yellow LiquidPeso molecular:119.16HIV-1 inhibitor-81
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.Fórmula:C32H44N2O8SCor e Forma:SolidPeso molecular:616.77Peptide T TFA
CAS:Peptide T (TFA), an octapeptide from HIV-1 gp120, inhibits HIV binding to CD4.Fórmula:C37H56F3N9O18Pureza:98%Cor e Forma:SolidPeso molecular:971.89HIV p17 Gag (77-85)
CAS:<p>Targeting HIV Gag p17 (77-85) with intracellular Ab cDNA disrupts viral replication pre/post-integration.</p>Fórmula:C44H72N10O15Pureza:98%Cor e Forma:SolidPeso molecular:981.1PNU-142721
CAS:PNU-142721, reverse transcriptase inhibitor, is used to treat human immunodeficiency virus (HIV) infection.Fórmula:C13H11ClN4OSCor e Forma:SolidPeso molecular:306.77
