Proteasa del VIH
Los inhibidores de la proteasa del VIH son una clase de fármacos antirretrovirales que atacan específicamente la enzima proteasa del virus de la inmunodeficiencia humana (VIH). Al inhibir esta enzima, estos compuestos evitan que el virus procese sus poliproteínas en proteínas maduras y funcionales, bloqueando así la producción de nuevos viriones infecciosos. Los inhibidores de la proteasa del VIH son una piedra angular de la terapia antirretroviral altamente activa (TARGA) utilizada para manejar el VIH/SIDA. En CymitQuimica, ofrecemos una variedad de inhibidores de la proteasa del VIH para apoyar su investigación en el tratamiento del VIH, la resistencia a los medicamentos y la virología.
Se han encontrado 449 productos de "Proteasa del VIH"
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Islatravir
CAS:<p>Islatravir (MK-8591) is an effective anti-HIV-1 agent.</p>Fórmula:C12H12FN5O3Pureza:98.77%Forma y color:SolidPeso molecular:293.25Nevirapine
CAS:<p>Nevirapine (NVP) is a benzodiazepine non-nucleoside reverse transcriptase inhibitor.</p>Fórmula:C15H14N4OPureza:99.58% - 99.59%Forma y color:White Or Off-White Crystalline PowderPeso molecular:266.3GSK2838232
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%Forma y color:SolidPeso molecular:809.56(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%Forma y color:SoildPeso molecular:294.35Zalcitabine
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%Forma y color:White To Off-White Crystalline PowderPeso molecular:211.223-Deazaadenosine hydrochloride
CAS:<p>3-Deazaadenosine HCl blocks SAH hydrolase (Ki: 3.9 μM), with anti-inflammatory, anti-proliferative, and anti-HIV effects.</p>Fórmula:C11H15ClN4O4Pureza:98.48%Forma y color:SolidPeso molecular:302.71BRD-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>Fórmula:C19H17N3O2SPureza:98.01% - 99.05%Forma y color:SolidPeso molecular: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>Fórmula:C19H23N4O6PSPureza:99.2% - 99.91%Forma y color:Shinning Black PowderPeso molecular:466.45Salicylanilide
CAS:<p>Salicylanilide (2-Hydroxybenzanilide)s are a group of compounds with antiviral potency, antibacterial and antifungal activities.</p>Fórmula:C13H11NO2Pureza:99.55%Forma y color:White To Off-White Crystalline PowderPeso molecular:213.23(Rac)-Telinavir
CAS:<p>N1 compound with anti-HIV activity; contains dimethyl, phenyl, quinoline groups.</p>Fórmula:C33H44N6O5Pureza:99.30%Forma y color:SolidPeso molecular:604.74Ibalizumab
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%Forma y color: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%Forma y color:SolidPeso molecular:425.52Fostemsavir 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>Fórmula:C29H37N8O11PPureza:99.45%Forma y color:SolidPeso molecular:704.62Atazanavir
CAS:<p>Atazanavir (BMS-232632)(BMS-232632) is an highly effective HIV-1 protease inhibitor.</p>Fórmula:C38H52N6O7Pureza:98% - 99.95%Forma y color:Crystalline SolidPeso molecular:704.86Tenofovir 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>Fórmula:C9H16N5O10P3·C6H15NPureza:93.45% - 98.51%Forma y color:SolidPeso molecular:548.36TERT-IN-1
CAS:<p>TERT-IN-1 has anti-HIV activity and can be used to study HIV infection.</p>Fórmula:C16H20ClN3SPureza:99.31%Forma y color:SoildPeso molecular:321.87NBD-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>Fórmula:C17H24ClN3O2Pureza:99.79%Forma y color:SolidPeso molecular:337.84Dolutegravir intermediate-1
CAS:<p>Dolutegravir intermediate-1 is a synthetic precursor for HIV-1 treatment from patent WO 2016125192 A2.</p>Fórmula:C13H17NO8Pureza:99.52%Forma y color:SolidPeso molecular:315.28Probenecid
CAS:<p>Probenecid (Benemid) is a benzoic acid derivative with antihyperuricemic property.</p>Fórmula:C13H19NO4SPureza:98.95% - 99.84%Forma y color:Crystals From Dil Alcohol Pleasant Aftertaste (Ntp 1992)Peso molecular: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>Fórmula:C16H11ClN6O3SPureza:99.07%Forma y color:SolidPeso molecular:402.81Elsulfavirine
CAS:<p>Elsulfavirine (VM-1500) is an HIV-1 infection reverse transcriptase inhibitor. It is a new anti-HIV drug.</p>Fórmula:C24H17BrCl2FN3O5SPureza:99.66%Forma y color:SolidPeso molecular:629.28Atazanavir sulfate
CAS:<p>Atazanavir sulfate, an azapeptide HIV-protease inhibitor, treats HIV/AIDS alongside other anti-HIV drugs.</p>Fórmula:C38H52N6O7·H2SO4Pureza:99.31% - 99.40%Forma y color:SolidPeso molecular:802.93Pepstatin
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>Fórmula:C34H63N5O9Pureza:96.74% - 99.94%Forma y color:SolidPeso molecular:685.89Ritonavir
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%Forma y color:White PowderPeso molecular:720.94Ditiocarb
CAS:<p>Ditiocarb speeds up copper cementation, cuts HIV risk, and boosts high-risk breast cancer immunoresearch.</p>Fórmula:C5H11NS2Forma y color:SolidPeso molecular:149.28Hinnuliquinone
CAS:Hinnuliquinone is an anti-HIV agent.Fórmula:C32H30N2O4Pureza:98%Forma y color:SolidPeso molecular:506.59SDZ 283-910
CAS:<p>SDZ 283-910 is used as a statine-derived inhibitor.</p>Fórmula:C46H59N5O9Pureza:98%Forma y color:SolidPeso molecular:826.004Ganoderic 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:C30H42O6Forma y color:SolidPeso molecular:498.65HIV-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>Forma y color:Odour SolidHIV 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>Fórmula:C94H134F3N27O25SForma y color:SolidPeso molecular:2131.29AL-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>Fórmula:C67H57N7O23Forma y color:SolidPeso molecular:1328.2Pentosan Polysulfate
CAS:<p>Pentosan Polysulfate: anti-HIV, anti-inflammatory, supports cartilage, treats interstitial cystitis.</p>Pureza:98%Forma y color:SolidPeso molecular:N/AProtease Inhibitor Library
<p>A unique collection of 343 protease and proteasome inhibitors for research in chemical genomics, and drug screening;</p>Forma y color:Odour SolidPol (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>Fórmula:C46H78N12O12Forma y color:SolidPeso molecular:991.181-Deoxymannojirimycin hydrochloride
CAS:<p>1-Deoxymannojirimycin hydrochloride is a selective α1,2-mannosidase inhibitor(IC50: 20 μM).</p>Fórmula:C6H14ClNO4Pureza:98%Forma y color:SolidPeso molecular:199.63RPR103611
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>Fórmula:C46H78N2O6Forma y color:SolidPeso molecular:755.12Pirmitegravir
CAS:<p>Pirmitegravir (STP0404) is a potent ALLINI, blocks LEDGF/p75 site, shows antiviral action against HIV.</p>Fórmula:C27H31ClN4O3Pureza:99.79% - 99.79%Forma y color:SolidPeso molecular:495.01AI 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>Fórmula:C21H24O4Pureza:99.01%Forma y color:SolidPeso molecular:340.41L 754394
CAS:<p>L 754394 is an effective and specific inhibitor of the HIV-1 protease.</p>Fórmula:C38H47N5O5Forma y color:SolidPeso molecular:653.81ICeD-2
<p>ICeD-2 triggers death in HIV-1 infected cells, requires HIV protease, inhibits DPP8/9, and stabilizes DPP9 in PBMCs.</p>Fórmula:C20H29N3OForma y color:SolidPeso molecular:327.46CTP518
CAS:<p>CTP518, a deuterated Atazanivir derivative, is a HIV protease inhibitor.</p>Fórmula:C38H52N6O7Pureza:98%Forma y color:SolidPeso molecular:719.95Diacetylsplenopentin HCl
CAS:<p>Diacetylsplenopentin HCl, a synthetic immunomodulator, aids healthy bone marrow stem cell growth without triggering harmful immune reactions.</p>Fórmula:C35H56ClN9O11Pureza:98%Forma y color:SolidPeso molecular:814.33Dihydroobionin B
<p>Dihydroobionin B exhibits potent (please insert the rest of the sentence for revision).</p>Fórmula:C21H26O5Forma y color:SolidPeso molecular:358.43Kadsuralignan 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>Fórmula:C22H26O7Forma y color:SolidPeso molecular:402.44KRH-3955 Salt
CAS:<p>KRH-3955, a CXCR4 antagonist, is an orally bioavailable and extremely potent inhibitor of HIV-1 infection.</p>Fórmula:C40H63N7O18Pureza:98%Forma y color:SolidPeso molecular:929.96MB-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>Forma y color:Odour LiquidHIV-1 inhibitor-11
<p>HIV-1 inhibitor-11, a fused pyridine ring derivative, is a HIV-1 inhibitor.</p>Fórmula:C42H36ClF10N7O5S2Forma y color:SolidPeso molecular:1008.35Morin 3-O-β-D-glucopyranoside
CAS:<p>Morin 3-O-β-D-glucopyranoside, a natural flavonoid, exhibits antifungal, anticancer, and antioxidant properties.</p>Fórmula:C21H20O12Forma y color:SolidPeso molecular:464.38CA inhibitor 1
CAS:<p>CA inhibitor 1 (GS-6207 analog) is a potent inhibitor of the HIV capsid.</p>Fórmula:C41H36ClF8N7O5S2Pureza:98%Forma y color:SolidPeso molecular:958.34Censavudine
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>Fórmula:C12H12N2O4Pureza:98%Forma y color:SolidPeso molecular:248.23SPD-756
CAS:<p>SPD-756, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C12H16N6O3Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C32H31N9O3SForma y color:SolidPeso molecular:621.711,6-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>Fórmula:C20H20O14Forma y color:SolidPeso molecular:484.366UK-88947 HCl
CAS:<p>UK 88947 is a protease inhibitor.</p>Fórmula:C41H63ClN6O6Pureza:98%Forma y color:SolidPeso molecular:771.44Bictegravir 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>Fórmula:C21H17F3N3NaO5Pureza:99.97%Forma y color:SolidPeso molecular:471.36Carbovir triphosphate
CAS:<p>Carbovir triphosphate (CBV-TP), a phosphorylated metabolite, serves as a research tool for studying human immunodeficiency virus (HIV) [1].</p>Fórmula:C11H16N5O11P3Forma y color:SolidPeso molecular:487.19HIV-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>Fórmula:C32H34N6O4SForma y color:SolidPeso molecular:598.72Delavirdine
CAS:<p>Delavirdine, an NNRTI for HIV-1, is used in HAART.</p>Fórmula:C22H28N6O3SForma y color:SolidPeso molecular:456.56Indoline
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>Fórmula:C8H9NForma y color:Clear To Yellow LiquidPeso molecular:119.16Ac-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>Fórmula:C38H58N10O12Forma y color:SolidPeso molecular:846.93NF279
CAS:<p>P2X1 antagonist</p>Fórmula:C49H36N6Na6O23S6Pureza:98%Forma y color:SolidPeso molecular:1407.17GP120, HIV-1 MN
GP120, HIV-1 MN, a peptide, is utilized in researching HIV infection [1] [2].Fórmula:C135H221N45O33Forma y color:SolidPeso molecular:3002.5BMS-955176 TFA
CAS:<p>GSK3532795: Oral HIV-1 maturation inhibitor, broad virus coverage, EC50: 15 nM, good preclinical pharmacokinetics.</p>Fórmula:C44H64N2O8SPureza:98%Forma y color:SolidPeso molecular:781.06Kuguacin N
<p>Kuguacin N is a useful organic compound for research related to life sciences and the catalog number is T126345.</p>Fórmula:C30H46O4Forma y color:SolidPeso molecular:470.694Elvucitabine
CAS:<p>Elvucitabine, a reverse transcriptase inhibitor, is used potentially for the treatment of HBV infection and HIV infection.</p>Fórmula:C9H10FN3O3Forma y color:SolidPeso molecular:227.19Kni 102
CAS:<p>Kni 102 is a biochemical.</p>Fórmula:C31H41N5O7Forma y color:SolidPeso molecular:595.6912-Oxocalanolide A
<p>12-Oxocalanolide A is a useful organic compound for research related to life sciences and the catalog number is T125675.</p>Fórmula:C22H24O5Forma y color:SolidPeso molecular:368.429TAT peptide
<p>TAT peptide, a CPP, delivers molecules into cells by traversing membrane barriers using aa49-57 of TAT protein.</p>Fórmula:C65H124N34O15Pureza:98%Forma y color:SolidPeso molecular:1621.91Alvircept sudotox
CAS:<p>Alvircept sudotox, a recombinant CD4 fused with exotoxin A from Pneumonas aeruginosa, is utilized in HIV infection research [1].</p>Forma y color:LiquidHIV-IN-2
CAS:<p>HIV-IN-2 (Compound 100) is a potent inhibitor of HIV, showing potential for research into HIV infection [1].</p>Fórmula:C34H27ClF7N9O3SForma y color:SolidPeso molecular:810.14Fluorescent HIV Substrate
CAS:<p>Fluorescent HIV Substrate is a HIV substrate.</p>Fórmula:C50H76N14O14Forma y color:SolidPeso molecular:1097.22N36Mut(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>Fórmula:C189H317N55O56Forma y color:SolidPeso molecular:4255.87Decanoyl-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:C36H67ClF3N11O7Forma y color:SolidPeso molecular:858.45Emtricitabine S-oxide
CAS:<p>Emtricitabine treats HIV; its degradation byproduct is Emtricitabine S-oxide.</p>Fórmula:C8H10FN3O4SPureza:98%Forma y color:SolidPeso molecular:263.25Acetyl-pepstatin
CAS:<p>Streptomyces pepsin inhibitor is used as a pepsin inhibitor.</p>Fórmula:C31H57N5O9Forma y color:SolidPeso molecular:643.81JE-2178
CAS:<p>JE-2178 is compound with high bioavailability .</p>Fórmula:C35H51N5O6SForma y color:SolidPeso molecular:669.87Clathrin-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%Forma y color:SolidPeso molecular:473.36Tenofovir-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>Fórmula:C28H52F3N6O5PForma y color:SolidPeso molecular:640.73Acetyl-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>Fórmula:C24H28O8Pureza:98%Forma y color:SolidPeso molecular:444.47HIV-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:C26H19N7OForma y color:SolidPeso molecular:445.475Decanoyl-RVKR-CMK
CAS:<p>Inhibits all seven proprotein convertases; stops proET-1 processing; hinders VGF secretion in PC12 cells.</p>Fórmula:C34H66ClN11O5Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C28H28FN5O3SForma y color:SolidPeso molecular: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>Fórmula:C37H46N4O6Forma y color:SolidPeso molecular:642.78Tenofovir-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>Fórmula:C29H55N6O5PSiForma y color:SolidPeso molecular:626.855HIV 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>Fórmula:C45H81N11O14S2Pureza:98%Forma y color:SolidPeso molecular:1064.32HIV-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>Forma y color:Odour SolidAureothin
CAS:<p>Aureothin: a nitroaryl polyketide with antitumor, antifungal & insecticidal properties; inhibits NADH:oxidoreductase (IC50s: 0.07-22 nmol/mg).</p>Fórmula:C22H23NO6Forma y color:SolidPeso molecular:397.42(+)-Carbovir triphosphate
CAS:<p>(+)-Carbovir triphosphate, Abacavir's active metabolite, studied for HIV-1 resistance and inhibition mechanisms.</p>Fórmula:C11H16N5O11P3Forma y color:SolidPeso molecular:487.19HIV-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>Fórmula:C32H44N2O8SForma y color:SolidPeso molecular:616.77Schineolignin B
<p>Schineolignin B is a useful organic compound for research related to life sciences and the catalog number is T126011.</p>Fórmula:C22H30O5Forma y color:SolidPeso molecular:374.477HIV-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>Fórmula:C25H20ClN3O3SForma y color:SolidPeso molecular: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>Fórmula:C19H18N2O4Forma y color:SolidPeso molecular:338.364-Acetylbutyric acid
CAS:<p>4-Acetylbutyric acid is a ketone acid widely used in biochemical experiments and drug synthesis research.</p>Fórmula:C6H10O3Pureza:99.88%Forma y color:SolidPeso molecular:130.14Cys-TAT(47-57)
CAS:<p>Cys-TAT(47-57): arginine-rich peptide from HIV-1 TAT protein's transduction domain.</p>Fórmula:C67H124N34O14SPureza:98%Forma y color:SolidPeso molecular:1661.99(2S,5S)-Censavudine
<p>(2S,5S)-Censavudine, a potent HIV inhibitor and nucleoside reverse transcriptase blocker.</p>Fórmula:C12H12N2O4Forma y color:SolidPeso molecular:248.23Peritassine A
CAS:<p>Peritassine A, an alkaloid derived from Tripterygium wilfordii Hook. f., exhibits anti-HIV properties.</p>Fórmula:C38H47NO18Forma y color:SolidPeso molecular:805.783Peptide T TFA
CAS:<p>Peptide T (TFA), an octapeptide from HIV-1 gp120, inhibits HIV binding to CD4.</p>Fórmula:C37H56F3N9O18Pureza:98%Forma y color:SolidPeso molecular:971.89Pegaldesleukin
CAS:<p>Pegaldesleukin, a PEG-IL2 conjugate, exhibits antiviral properties, potentially slowing HIV progression, preserving immune function.</p>Forma y color:LiquidLenacapavir sodium
CAS:Lenacapavir, also known as GS-6207, is an HIV-1 capsid inhibitor. It demonstrates an average EC50 of 50 pM (ranging from 20-160 pM) against 23 clinical isolates of HIV-1 from diverse subtypes, with tests performed in peripheral blood mononuclear cells (PBMCs). In vitro, Lenacapavir exhibits picomolar potency and shows no cross-resistance with existing antiretroviral compounds. Furthermore, Lenacapavir displays significant antiviral activity in individuals with HIV-1, regardless of prior treatment history, with no pre-existing resistance detected.Fórmula:C39H31ClF10N7NaO5S2Peso molecular:990.26HIV-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%Forma y color:SolidPeso molecular: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>Fórmula:C44H72N10O15Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C41H47NO19Forma y color:SolidPeso molecular:857.81PROTAC 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>Forma y color:Odour SolidScirpusin A
CAS:<p>Scirpusin A is a hydroxystilbene dimer from the rhizome of Scirpus fluviatilis and Xinjiang wine grape.</p>Fórmula:C28H22O7Forma y color:SolidPeso molecular: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>Fórmula:C26H24N6O2Forma y color:SolidPeso molecular: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>Fórmula:C20H17NO2Forma y color:SolidPeso molecular:303.35Inophyllum 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>Fórmula:C25H24O5Forma y color:SolidPeso molecular:404.46HIV-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%Forma y color:SolidPeso molecular:396.56HIV 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>Fórmula:C39H40ClF7N10O7Forma y color:SolidPeso molecular:929.24HIV-1 protease-IN-4
<p>HIV-1 protease-IN-4, a prodrug of atazanavir, delivers 5x AUC & 67x C24 compared to atazanavir.</p>Fórmula:C48H69N7O11Forma y color:SolidPeso molecular:920.1PNU-142721
CAS:<p>PNU-142721, reverse transcriptase inhibitor, is used to treat human immunodeficiency virus (HIV) infection.</p>Fórmula:C13H11ClN4OSForma y color:SolidPeso molecular:306.77HIV-1 inhibitor-12
<p>HIV-1 inhibitor-12: potent at inhibiting HIV-1 capsid protein polymerization with 9 nM IC50.</p>Fórmula:C42H36ClF10N7O5S2Forma y color:SolidPeso molecular:1008.35VRC01LS
<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>Forma y color:Odour Liquidgp120-α4β7 binding inhibitor 11
CAS:<p>gp120-α4β7 binding inhibitor 11 is an anti-HIV agent.</p>Fórmula:C26H27N3O2Pureza:98.57%Forma y color:SolidPeso molecular:413.51NNRTIs-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>Fórmula:C17H20ClN5OPureza:98%Forma y color:SolidPeso molecular:345.83HIV-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>Fórmula:C40H45N7O4Forma y color:SolidPeso molecular:687.83(-)-Rabdosiin
CAS:<p>(-)-Rabdosiin, identified as a novel phenolic marker in Symphytum officinale L., exhibits antioxidant, neuroprotective, and anti-HIV activities [1].</p>Fórmula:C36H30O16Forma y color:SolidPeso molecular:718.61Clavirolide L
<p>Clavirolide L (Compound 3), a dolabellane-type diterpenoid isolated from Clavularia viridis, demonstrates significant inhibition against HIV-1 without</p>Fórmula:C20H28O3Forma y color:SolidPeso molecular:316.43Cyclotriazadisulfonamide hydrochloride
CAS:<p>Cyclotriazadisulfonamide HCl blocks HIV entry by hindering CD4 translocation into the ER.</p>Fórmula:C31H40ClN3O4S2Pureza:98%Forma y color:SolidPeso molecular:618.25Antitumor 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:C22H14N12S2Forma y color:SolidPeso molecular:510.557BNM-III-170
CAS:<p>BNM-III-170 is able to inhibit HIV-1 viral entry into target cells.</p>Fórmula:C25H26ClF7N6O6Forma y color:SolidPeso molecular: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>Fórmula:C35H55N9O16Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C27H30O8Forma y color:SolidPeso molecular:482.52VIR-165
<p>VIR-165, a derivative of VIRIP (353-372 of alpha1-antitrypsin), blocks several HIV-1 strains.</p>Fórmula:C109H158N22O25S2Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C20H17ClN3O3PPureza:99.93%Forma y color:SoildPeso molecular:413.79Amdoxovir
CAS:<p>Amdoxovir is a reverse transcriptase inhibitor.</p>Fórmula:C9H12N6O3Forma y color:SolidPeso molecular:252.23Mk-6186 HCl
<p>MK-6186 HCl, a novel non-nucleoside reverse transcriptase inhibitor with antiviral activity, can be used to study HIV.</p>Fórmula:C21H13Cl3N6OPureza:98.19%Forma y color:SoildPeso molecular:471.73[(Cys(Bzl)84,Glu(OBzl)85)]CD4 (81-92)
CAS:[(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].Fórmula:C76H108N14O26SForma y color:SolidPeso molecular:1665.81MPG, HIV related
CAS:<p>MPG: 27-amino acid peptide from HIV-1 gp41 & SV40 T antigen, delivers nucleic acids into cells efficiently.</p>Fórmula:C126H201N35O33SPureza:98%Forma y color:SolidPeso molecular:2766.224-Deoxy-4α-phorbol
CAS:<p>4-Deoxy-4α-phorbol, a tetracyclic diterpene identified in E.</p>Fórmula:C20H28O5Forma y color:SolidPeso molecular:348.43Globotriaosylceramides (porcine)
CAS:<p>Globotriaosylceramides, cell membrane glycosphingolipids, act as Shiga toxin receptors and accumulate in Fabry disease, resisting HIV by blocking gp120.</p>Fórmula:C60H113NO18Forma y color:SolidPeso molecular:1136.553Enfuvirtide
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>Fórmula:C204H301N51O64Pureza:98%Forma y color:White To Off-White Amorphous SolidPeso molecular:4491.945Epicoccone 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>Fórmula:C9H8O5Forma y color:SolidPeso molecular:196.16JE-2147
CAS:<p>JE-2147: a hybrid peptide with multiple amino acid types linked by peptide bonds.</p>Fórmula:C32H37N3O5SForma y color:SolidPeso molecular:575.72GLR-19
CAS:<p>GLR-19 is an anti-HIV peptide with demonstrated antiviral activity against HSV-2 [1] [2].</p>Fórmula:C102H194N40O20Pureza:98%Forma y color:SolidPeso molecular:2300.89QYL-685
CAS:<p>QYL-685 is a methylenecyclopropane nucleoside analog.</p>Fórmula:C20H24N7O5PForma y color:SolidPeso molecular:473.42(±)-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>Fórmula:C25H27NO4Forma y color:SolidPeso molecular:405.49Abacavir hydroxyacetate
CAS:<p>Abacavir hydroxyacetate is a nucleoside analog reverse transcriptase inhibitor used in the study of HIV infection.</p>Fórmula:C16H20N6O3Pureza:98.29%Forma y color:SolidPeso molecular:344.37Pentosan Polysulfate Sodium (W/W 43%)
CAS:<p>Pentosan Polysulfate Sodium: anti-HIV, anti-inflammatory, aids cartilage, treats interstitial cystitis.</p>Pureza:98%Forma y color:SolidPeso molecular:N/ADideoxyadenosine
CAS:<p>2',3'-Dideoxyadenosine is an inhibitor of HIV replication with antiretroviral activity and antiviral efficacy [1].</p>Fórmula:C10H13N5O2Pureza:99.28%Forma y color:Physical Description Off-White Powder (Ntp 1992)Peso molecular: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>Fórmula:C10H12FN5O3Pureza:99.95%Forma y color:SolidPeso molecular:269.23Pseudothymidine
CAS:<p>Pseudothymidine is a C-nucleoside analog of thymidine.</p>Fórmula:C10H14N2O5Pureza:98%Forma y color:SolidPeso molecular:242.23(Z)-9-Propenyladenine
CAS:<p>(Z)-9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate.</p>Fórmula:C8H9N5Forma y color:SolidPeso molecular:175.19TAT (48-57)
CAS:<p>TAT (48-57) is a cell-permeable HIV-1 Tat protein fragment, amino acids 48-57.</p>Fórmula:C55H109N31O12Pureza:98%Forma y color:SolidPeso molecular:1396.65Etravirine 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>Fórmula:C20H15BrN6OPureza:98%Forma y color:SolidPeso molecular:439.3Letrazuril
CAS:<p>Letrazuril is a compound of the anti-HIV.</p>Fórmula:C17H9Cl2FN4O2Forma y color:SolidPeso molecular:391.18Cabotegravir sodium
CAS:<p>Cabotegravir sodium inhibits HIV integrase (IC50: 2.5 nM), metabolized by UGT1A1, with minimal ARV interaction.</p>Fórmula:C19H16F2N3NaO5Forma y color:SolidPeso molecular:427.34PL 100
CAS:<p>PL 100 could inhibit HIV-1 protease.</p>Fórmula:C33H44N4O6SPureza:98%Forma y color:SolidPeso molecular:624.79Tenofovir hydrate
CAS:<p>Tenofovir hydrate (GS 1278 hydrate) is a nucleotide reverse transcriptase inhibitor with antiviral activity.</p>Fórmula:C9H16N5O5PPureza:99.63%Forma y color:SolidPeso molecular:305.239-Propenyladenine
CAS:<p>9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate.</p>Fórmula:C8H9N5Forma y color:SolidPeso molecular: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>Fórmula:C21H25F6N5O5Forma y color:SolidPeso molecular:541.44Saquinavir mesylate
CAS:<p>Saquinavir mesylate (Ro 31-8959/003) is an Inhibitor of HIV Proteaseused in antiretroviral therapy</p>Fórmula:C39H54N6O8SPureza:99.19%Forma y color:White Or Pale Yellow PowderPeso molecular:766.9Betulin diacetate
CAS:<p>Betulin diacetate is a bioactive chemical.</p>Fórmula:C34H54O4Forma y color:SolidPeso molecular:526.8Ditiocarb 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>Fórmula:C5H10NNaS2Pureza:98.04%Forma y color:White Solid CrystallinePeso molecular:171.26Amprenavir
CAS:<p>Amprenavir (KVX-478) is a synthetic derivative of hydroxyethylamine sulfonamide that selectively binds to and inhibits human immunodeficiency virus (HIV)</p>Fórmula:C25H35N3O6SPureza:99.60% - 99.87%Forma y color:Off-White To Pale YellowPeso molecular:505.63Delavirdine mesylate
CAS:<p>Delavirdine mesylate (BHAP-U 90152 (mesylate)) is a non-nucleoside reverse transcriptase inhibitor (NNRTI).</p>Fórmula:C23H32N6O6S2Pureza:99.99%Forma y color:Light Brown SolidPeso molecular:552.67Tenofovir alafenamide
CAS:<p>Tenofovir alafenamide (GS-7340) is a nucleotide reverse transcriptase inhibitor (NRTI) and a novel ester prodrug of the antiretroviral tenofovir.</p>Fórmula:C21H29N6O5PPureza:99.68% - 99.81%Forma y color:SolidPeso molecular:476.47Dolutegravir 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>Fórmula:C20H18F2N3NaO5Pureza:98% - 99.46%Forma y color:SolidPeso molecular:441.36Escin 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>Fórmula:C55H86O24Pureza:98.97% - 99.81%Forma y color:SolidPeso molecular:1131.26Doravirine
CAS:<p>Doravirine (MK-1439) is a non-nucleoside reverse transcriptase inhibitor, used in the treatment of HIV/AIDS.</p>Fórmula:C17H11ClF3N5O3Pureza:99.65% - 99.79%Forma y color:SolidPeso molecular:425.75Cobicistat
CAS:<p>Cobicistat (GS-9350): A carbamate, thiazole derivative, and CYP3A inhibitor used to boost anti-HIV drugs for treating HIV.</p>Fórmula:C40H53N7O5S2Pureza:97.36% - 99.62%Forma y color:SolidPeso molecular:776.02Lopinavir
CAS:<p>Lopinavir (ABT-378) is a peptidomimetic HIV protease inhibitor that retains activity against HIV protease with the Val 82 mutation.</p>Fórmula:C37H48N4O5Pureza:98% - 99.62%Forma y color:White Crystalline SolidPeso molecular:628.8Raltegravir sodium
CAS:<p>Raltegravir (MK 0518) sodium is a potent, orally active HIV integrase (IN) inhibitor.</p>Fórmula:C20H20FN6NaO5Forma y color:SolidPeso molecular:466.405Amylmetacresol
CAS:<p>Amylmetacresol treats sore throat, pharyngitis, tonsillitis, laryngitis, influenza A, and SARS-CoV.</p>Fórmula:C12H18OPureza:99.66%Forma y color:SolidPeso molecular:178.27Dolutegravir
CAS:<p>Dolutegravir (GSK1349572), HIV integrase inhibitor with IC50 of 2.7 nM, partly effective against some raltegravir-resistant HIV strains.</p>Fórmula:C20H19F2N3O5Pureza:98.97% - 99.75%Forma y color:White To Pale Yellow SolidPeso molecular:419.38Didanosine
CAS:<p>Didanosine (ddI) is a nucleoside reverse transcriptase inhibitor analog of adenosine (IC50: 0.49 μM).</p>Fórmula:C10H12N4O3Pureza:99.64%Forma y color:White Crystalline PowderPeso molecular:236.23Ganoderic acid B
CAS:<p>Ganoderic acid B: quality marker for G. lucidum products, inhibits telomerase & EBV activation, moderates HIV-1 protease.</p>Fórmula:C30H44O7Pureza:99.09% - 99.95%Forma y color:SolidPeso molecular:516.67Darunavir
CAS:<p>Darunavir (TMC114) is an HIV PROTEASE INHIBITOR that is used in the treatment of AIDS and HIV INFECTIONS.</p>Fórmula:C27H37N3O7SPureza:99.67% - 99.76%Forma y color:White Amorphous SolidPeso molecular:547.66Temsavir
CAS:<p>Temsavir (BMS626529) is a novel attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T cells.</p>Fórmula:C24H23N7O4Pureza:99.14%Forma y color:SolidPeso molecular:473.48BMS-707035
CAS:<p>BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.</p>Fórmula:C17H19FN4O5SPureza:99.78%Forma y color:SolidPeso molecular:410.42TAT
CAS:<p>TAT peptide (YGRKKRRQRRR), originating from the human immunodeficiency virus-1 (HIV-1) transactivator of transcription (TAT), enhances the solubility and</p>Fórmula:C64H118N32O14Pureza:>99.99%Forma y color:SolidPeso molecular:1559.83Raltegravir
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>Fórmula:C20H21FN6O5Pureza:99.86% - >99.99%Forma y color:SolidPeso molecular:444.42NBD-557
CAS:<p>NBD-557 is a potentially HIV-1 inhibitor.</p>Fórmula:C17H24BrN3O2Pureza:99.52%Forma y color:SolidPeso molecular:382.3I-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>Fórmula:C22H16N2NaO2Forma y color:SolidPeso molecular:363.372LDC4297 hydrochloride
CAS:<p>LDC4297 hydrochloride is a selective and potent CDK7 inhibitor with broad-spectrum antiviral activity, useful for research on viral infections.</p>Fórmula:C23H29ClN8OForma y color:SolidPeso molecular:468.98Darunavir Ethanolate
CAS:<p>Darunavir Ethanolate (UIC 94017) is an HIV PROTEASE INHIBITOR that is used in the treatment of AIDS and HIV INFECTIONS.</p>Fórmula:C29H43N3O8SPureza:99.84% - 99.86%Forma y color:SolidPeso molecular:593.742,4-Dihydroxypyridine
CAS:<p>2,4-Dihydroxypyridine: a pyridine derivative, chelates metals, assesses ion levels, measures enzymatic reactions, and quantifies biomolecules.</p>Fórmula:C5H5NO2Pureza:97.79%Forma y color:White To Yellow-Beige Crystals OrPeso molecular:111.1Rosamultin
CAS:<p>Rosamultin has antioxidant, antiinflammatory/antinociceptive properties,and has anti-human immunodeficiency virus (HIV) activity.</p>Fórmula:C36H58O10Pureza:98% - 99.83%Forma y color:SolidPeso molecular:650.84Thiamine 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>Fórmula:C24H34N8O4S2Pureza:99.81%Forma y color:CoaPeso molecular: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>Fórmula:C52H78N10O17Pureza:99.78% - 99.91%Forma y color:SolidPeso molecular: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>Fórmula:C20H20FN6O5·KPureza:98% - 99.55%Forma y color:Off-White SolidPeso molecular:482.51Rolipram
CAS:<p>Rolipram (SB 95952) is a phosphodiesterase 4 inhibitor with antidepressant properties.</p>Fórmula:C16H21NO3Pureza:99.22% - >99.99%Forma y color:SolidPeso molecular:275.34IMB-301
CAS:<p>IMB-301 is a small molecular inhibitor via virtual screening according to the hA3G model.</p>Fórmula:C19H17Cl2FN2OPureza:99.72%Forma y color:SolidPeso molecular:379.26PMEDAP
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>Fórmula:C8H13N6O4PPureza:99.77%Forma y color:SolidPeso molecular: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>Fórmula:C3H8OS2Pureza:98.91% - 99.64%Forma y color:Viscous Oily LiquidPeso molecular:124.22PTACH
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>Fórmula:C20H26N2O2S2Pureza:87.44% - 99.74%Forma y color:SolidPeso molecular:390.56Peldesine 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>Fórmula:C12H13Cl2N5OForma y color:SolidPeso molecular:314.17Fostemsavir
CAS:<p>Fostemsavir (BMS-663068) is an HIV-1 attachment inhibitor in development for the treatment of HIV-1 infection.</p>Fórmula:C25H26N7O8PPureza:98.95%Forma y color:SolidPeso molecular:583.49Bictegravir
CAS:<p>Bictegravir (GS-9883) is a potent inhibitor of HIV-1 integrase (IC50: 7.5 nM).</p>Fórmula:C21H18F3N3O5Pureza:97.6% - 99.51%Forma y color:SolidPeso molecular:449.38HODHBt
CAS:<p>HODHBt is a STAT5-SUMO protein-protein interaction inhibitor.</p>Fórmula:C7H5N3O2Pureza:99.45% - 99.95%Forma y color:Off-White To Yellow SolidPeso molecular: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>Fórmula:C22H18N6Pureza:97.22% - 98.83%Forma y color:SolidPeso molecular:366.42Tenofovir alafenamide hemifumarate
CAS:<p>Tenofovir alafenamide hemifumarate (GS-7340 hemifumarate) is an oral phosphonoamidate prodrug of the HIV reverse transcriptase nucleotide inhibitor tenofovir.</p>Fórmula:C21H29N6O5PC4H4O4Pureza:99.33% - 99.96%Forma y color:SolidPeso molecular:534.51Des(benzylpyridyl) Atazanavi
CAS:<p>The N-dealkylated metabolite (M1) of Atazanavir, a HIV protease inhibitor.</p>Fórmula:C26H43N5O7Pureza:98% - 99.75%Forma y color:SolidPeso molecular: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>Fórmula:C38H50N6O5Pureza:99.50% - >99.99%Forma y color:SolidPeso molecular:670.84Dexelvucitabine
CAS:<p>Dexelvucitabine (RVT), a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C9H10FN3O3Pureza:98.25%Forma y color:SolidPeso molecular:227.19HIV-1 Inhibitor 18A
CAS:<p>HIV-1 Inhibitor 18A (HIV-1 Inhibitor-18A) specifically inhibits the entry of multiple HIV-1 isolates.</p>Fórmula:C14H11N5O2SPureza:99.79%Forma y color:SolidPeso molecular:313.33Etravirine
CAS:<p>Etravirine (R165335) is a diarylpyrimidine non-nucleoside reverse transcriptase inhibitor.</p>Fórmula:C20H15BrN6OPureza:97.61% - 99.74%Forma y color:White To Off-White SolidPeso molecular:435.28HIV-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>Fórmula:C18H16O2Pureza:99.90%Forma y color:SolidPeso molecular:264.32Elvitegravir
CAS:<p>Elvitegravir (JTK-303) is an HIV integrase inhibitor and CYP2C9 inducer.</p>Fórmula:C23H23ClFNO5Pureza:98.43% - 99.57%Forma y color:SolidPeso molecular:447.88Obefazimod
CAS:<p>Obefazimod (ABX-464) is a potent anti-HIV agent. ABX464 inhibits HIV-1 replication in stimulated peripheral blood mononuclear cells (PBMCs).</p>Fórmula:C16H10ClF3N2OPureza:99.86%Forma y color:SolidPeso molecular:338.71
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