
HIV Protease
Found 503 products of "HIV Protease"
Atazanavir sulfate
CAS:Atazanavir sulfate, an azapeptide HIV-protease inhibitor, treats HIV/AIDS alongside other anti-HIV drugs.Formula:C38H52N6O7·H2SO4Purity:99.31% - 99.40%Color and Shape:SolidMolecular weight:802.93Ref: TM-T0100
5mg44.00€10mg58.00€25mg90.00€50mg114.00€100mg170.00€200mg250.00€500mg425.00€1mL*10mM (DMSO)50.00€Islatravir
CAS:Islatravir (MK-8591) is an effective anti-HIV-1 agent.Formula:C12H12FN5O3Purity:98.77%Color and Shape:SolidMolecular weight:293.25Ref: TM-T16098
1mg75.00€5mg161.00€10mg245.00€25mg430.00€50mg583.00€100mg783.00€200mg1,054.00€1mL*10mM (DMSO)172.00€Ritonavir
CAS:Ritonavir (ABT 538) inhibits HIV-1/2 proteases; serum proteins limit it but it enhances other HIV drugs by hindering P450 degradation.Formula:C37H48N6O5S2Purity:99.38% - 99.96%Color and Shape:White PowderMolecular weight:720.94Ref: TM-T1525
1g475.00€5mg34.00€10mg50.00€25mg74.00€50mg96.00€100mg138.00€200mg192.00€500mg321.00€1mL*10mM (DMSO)50.00€PF-3450074
CAS:PF-3450074 (PF-74) is a specific HIV-1 inhibitor, blocking viral replication and uncoating at submicromolar EC50=8-640 nM.Formula:C27H27N3O2Purity:99.92%Color and Shape:SolidMolecular weight:425.52Benfotiamine
CAS:Benfotiamine (S-Benzoylthiamine O-monophosphate) is a synthetic S-acyl derivative of thiamine (vitamin B1), used as an antioxidant dietary supplement.Formula:C19H23N4O6PSPurity:99.2% - 99.91%Color and Shape:Shinning Black PowderMolecular weight:466.45(S)-(+)-N-3-Benzylnirvanol
CAS:(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.Formula:C18H18N2O2Purity:98.90%Color and Shape:SoildMolecular weight:294.35Fostemsavir Tris
CAS:Fostemsavir Tris (BMS-663068 Tris) is the prodrug of BMS-626529,is a oral, safe and effective inhibitor of HIV-1 attachment.Formula:C29H37N8O11PPurity:99.45%Color and Shape:SolidMolecular weight:704.62Ref: TM-T10570
1mg54.00€5mg114.00€10mg167.00€25mg268.00€50mg409.00€100mg580.00€1mL*10mM (DMSO)170.00€GSK2838232
CAS:GSK2838232 inhibit HIV reverse transcriptase activity across a broad panel of HIV-1 isolates,GSK2838232 is novel human immune virus (HIV) maturation inhibitor.
Formula:C48H73ClN2O6Purity:97.97%Color and Shape:SolidMolecular weight:809.56Dolutegravir intermediate-1
CAS:Dolutegravir intermediate-1 is a synthetic precursor for HIV-1 treatment from patent WO 2016125192 A2.Formula:C13H17NO8Purity:99.52%Color and Shape:SolidMolecular weight:315.28Salicylanilide
CAS:Salicylanilide (2-Hydroxybenzanilide)s are a group of compounds with antiviral potency, antibacterial and antifungal activities.Formula:C13H11NO2Purity:99.55%Color and Shape:White To Off-White Crystalline PowderMolecular weight:213.23Zalcitabine
CAS:Zalcitabine (ddC) is a nucleoside analog inhibiting HIV by blocking reverse transcriptase and halting viral DNA synthesis.Formula:C9H13N3O3Purity:99.08% - ≥95%Color and Shape:White To Off-White Crystalline PowderMolecular weight:211.22Sodium copper chlorophyllin B
CAS:Sodium copper chlorophyllin B exerts antiviral activities against Influenza virus and HIV.Formula:C34H29CuN4Na3O7Purity:≥98%Color and Shape:Green To Black PowderMolecular weight:738.13NBD-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.Formula:C17H24ClN3O2Purity:99.79%Color and Shape:SolidMolecular weight:337.84(Rac)-Telinavir
CAS:N1 compound with anti-HIV activity; contains dimethyl, phenyl, quinoline groups.
Formula:C33H44N6O5Purity:99.30%Color and Shape:SolidMolecular weight:604.74Atazanavir
CAS:Atazanavir (BMS-232632)(BMS-232632) is an highly effective HIV-1 protease inhibitor.Formula:C38H52N6O7Purity:98% - 99.95%Color and Shape:Crystalline SolidMolecular weight:704.86TERT-IN-1
CAS:TERT-IN-1 has anti-HIV activity and can be used to study HIV infection.Formula:C16H20ClN3SPurity:99.31%Color and Shape:SoildMolecular weight:321.87Probenecid
CAS:Probenecid (Benemid) is a benzoic acid derivative with antihyperuricemic property.Formula:C13H19NO4SPurity:98.95% - 99.84%Color and Shape:Crystals From Dil Alcohol Pleasant Aftertaste (Ntp 1992)Molecular weight:285.36Elsulfavirine
CAS:Elsulfavirine (VM-1500) is an HIV-1 infection reverse transcriptase inhibitor. It is a new anti-HIV drug.Formula:C24H17BrCl2FN3O5SPurity:99.66%Color and Shape:SolidMolecular weight:629.28Ref: TM-T15210
1mg69.00€5mg147.00€10mg230.00€25mg462.00€50mg692.00€100mg973.00€1mL*10mM (DMSO)200.00€3-Deazaadenosine hydrochloride
CAS:3-Deazaadenosine HCl blocks SAH hydrolase (Ki: 3.9 μM), with anti-inflammatory, anti-proliferative, and anti-HIV effects.Formula:C11H15ClN4O4Purity:98.48%Color and Shape:SolidMolecular weight:302.71Ref: TM-T10111
1mg119.00€5mg205.00€10mg354.00€25mg587.00€50mg822.00€100mg1,108.00€1mL*10mM (DMSO)141.00€Pepstatin
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.Formula:C34H63N5O9Purity:96.74% - 99.94%Color and Shape:SolidMolecular weight:685.89Nevirapine
CAS:Nevirapine (NVP) is a benzodiazepine non-nucleoside reverse transcriptase inhibitor.Formula:C15H14N4OPurity:99.58% - 99.59%Color and Shape:White Or Off-White Crystalline PowderMolecular weight:266.3Ibalizumab
CAS: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
Purity:SDS-PAGE:96.4%;SEC-HPLC:97.7%Color and Shape:LiquidMolecular weight:147.3 kDaAI 3-16787
CAS:AI 3-16787 is an HIV-1 integrase inhibitor exhibiting inhibitory activity against strand transfer in the presence of Mn²⁺.Formula:C21H24O4Purity:99.01%Color and Shape:SolidMolecular weight:340.41Dihydroobionin B
Dihydroobionin B exhibits potent (please insert the rest of the sentence for revision).Formula:C21H26O5Color and Shape:SolidMolecular weight:358.43Capsid assembly inhibitor
CAS:Capsid assembly inhibitor is a 12-mer peptide that binds to the Gag capsid (CA) domain, effectively inhibiting the assembly of both immature and mature-like HIV-1 capsid particles in vitro.Formula:C69H96N12O22Color and Shape:SolidMolecular weight:1445.57GP120, HIV-1 MN
GP120, HIV-1 MN, a peptide, is utilized in researching HIV infection [1] [2].Formula:C135H221N45O33Color and Shape:SolidMolecular weight:3002.5Elvucitabine
CAS:Elvucitabine, a reverse transcriptase inhibitor, is used potentially for the treatment of HBV infection and HIV infection.Formula:C9H10FN3O3Color and Shape:SolidMolecular weight:227.19PNU-142721
CAS:PNU-142721, reverse transcriptase inhibitor, is used to treat human immunodeficiency virus (HIV) infection.Formula:C13H11ClN4OSColor and Shape:SolidMolecular weight:306.77Epicoccone B
CAS:Epicoccone B from C. globosum has DPPH scavenging (IC50=10.8μM) and α-glucosidase inhibition (IC50=27.3μM), also anti-HIV.Formula:C9H8O5Color and Shape:SolidMolecular weight:196.16Kadsuralignan A
CAS:Kadsuralignan A (compound 1), a dibenzocyclooctadiene lignan extracted from the leaves and stems of Schisandra lancifolia, exhibits anti-HIV activity, with anFormula:C22H26O7Color and Shape:SolidMolecular weight:402.44Inophyllum B
CAS:(+)-Inophyllum B, an HIV Reverse Transcriptase inhibitor, IC50: 38 nM; blocks HIV-1 in vitro, IC50: 1.4 μM; from Achatina fulica.Formula:C25H24O5Color and Shape:SolidMolecular weight:404.46HIV Protease Substrate 1 TFA
HIV Protease Substrate 1 TFA, a fluorogenic substrate for HIV protease, facilitates the investigation of the enzyme's activity [1].Formula:C94H134F3N27O25SColor and Shape:SolidMolecular weight:2131.29Protease Inhibitor Library
A unique collection of 343 protease and proteasome inhibitors for research in chemical genomics, and drug screening;Color and Shape:Odour SolidRef: TM-L1100
1mgTo inquire30μL*10mM (DMSO)To inquire50μL*10mM (DMSO)To inquire100μL*10mM (DMSO)To inquire250μL*10mM (DMSO)To inquireJE-2178
CAS:JE-2178 is compound with high bioavailability .Formula:C35H51N5O6SColor and Shape:SolidMolecular weight:669.87HIV-1 inhibitor-80
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.Formula:C26H19N7OColor and Shape:SolidMolecular weight:445.475Decanoyl-RVKR-CMK TFA
CAS:Decanoyl-RVKR-CMK (DecRVKRcmk) TFA effectively hinders the processing of over-expressed gp160 and suppresses HIV-1 replication.
Formula:C36H67ClF3N11O7Color and Shape:SolidMolecular weight:858.45Clathrin-IN-1
CAS:Pitstop 2 inhibits clathrin-mediated endocytosis, targeting clathrin's terminal domain, with potential in cancer research.
Formula:C20H13BrN2O3S2Purity:99.53%Color and Shape:SolidMolecular weight:473.36Pol (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 (Formula:C46H78N12O12Color and Shape:SolidMolecular weight:991.18Ganoderic acid GS-1
CAS:Ganoderic acid GS-1, an extensively oxygenated lanostane-type triterpenoid, exhibits anti-HIV-1 protease activities, displaying an IC50 value of 58 μM [1].Formula:C30H42O6Color and Shape:SolidMolecular weight:498.65[(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].Formula:C76H108N14O26SColor and Shape:SolidMolecular weight:1665.81Aureothin
CAS:Aureothin: a nitroaryl polyketide with antitumor, antifungal & insecticidal properties; inhibits NADH:oxidoreductase (IC50s: 0.07-22 nmol/mg).Formula:C22H23NO6Color and Shape:SolidMolecular weight:397.42HIV-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.Color and Shape:Odour SolidVRC01LS
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.
Color and Shape:Odour Liquid(2S,5S)-Censavudine
(2S,5S)-Censavudine, a potent HIV inhibitor and nucleoside reverse transcriptase blocker.Formula:C12H12N2O4Color and Shape:SolidMolecular weight:248.23HIV-1 inhibitor-6
CAS: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 splicingFormula:C14H10N4O4SPurity:99.33%Color and Shape:SolidMolecular weight:330.32Antitumor agent-191
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.Formula:C22H14N12S2Color and Shape:SolidMolecular weight:510.557HIV p17 Gag (77-85)
CAS:Targeting HIV Gag p17 (77-85) with intracellular Ab cDNA disrupts viral replication pre/post-integration.Formula:C44H72N10O15Purity:98%Color and Shape:SolidMolecular weight:981.1Tenofovir-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.Formula:C28H52F3N6O5PColor and Shape:SolidMolecular weight:640.73SPD-756
CAS:SPD-756, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.Formula:C12H16N6O3Purity:98%Color and Shape:SolidMolecular weight: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.Formula:C32H31N9O3SColor and Shape:SolidMolecular weight:621.71JE-2147
CAS:JE-2147: a hybrid peptide with multiple amino acid types linked by peptide bonds.Formula:C32H37N3O5SColor and Shape:SolidMolecular weight:575.72(-)-Rabdosiin
CAS:(-)-Rabdosiin, identified as a novel phenolic marker in Symphytum officinale L., exhibits antioxidant, neuroprotective, and anti-HIV activities [1].Formula:C36H30O16Color and Shape:SolidMolecular weight:718.61HIV-1 protease-IN-4
HIV-1 protease-IN-4, a prodrug of atazanavir, delivers 5x AUC & 67x C24 compared to atazanavir.Formula:C48H69N7O11Color and Shape:SolidMolecular weight:920.14-Deoxy-4α-phorbol
CAS:4-Deoxy-4α-phorbol, a tetracyclic diterpene identified in E.Formula:C20H28O5Color and Shape:SolidMolecular weight:348.43Bictegravir Sodium
CAS:Bictegravir Sodium is an HIV-1 integrase inhibitor with 7.5 nM IC50, offering strong, selective anti-HIV effects and minimal toxicity.Formula:C21H17F3N3NaO5Purity:99.97%Color and Shape:SolidMolecular weight:471.36MPG, HIV related
CAS:MPG: 27-amino acid peptide from HIV-1 gp41 & SV40 T antigen, delivers nucleic acids into cells efficiently.Formula:C126H201N35O33SPurity:98%Color and Shape:SolidMolecular weight:2766.22HIV-1 protease-IN-14
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.Color and Shape:Odour SolidTenofovir-C3-O-C12-trimethylsilylacetylene ammonium
CAS:Tenofovir-C3-O-C12 has a longer half-life, potent anti-HIV effects, and better pharmacokinetics than tenofovir.Formula:C29H55N6O5PSiColor and Shape:SolidMolecular weight:626.855Schineolignin B
Schineolignin B is a useful organic compound for research related to life sciences and the catalog number is T126011.Formula:C22H30O5Color and Shape:SolidMolecular weight:374.477VIR-165
VIR-165, a derivative of VIRIP (353-372 of alpha1-antitrypsin), blocks several HIV-1 strains.Formula:C109H158N22O25S2Purity:98%Color and Shape:SolidMolecular weight:2240.7NF279
CAS:P2X1 antagonistFormula:C49H36N6Na6O23S6Purity:98%Color and Shape:SolidMolecular weight:1407.17HIV 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].Formula:C39H40ClF7N10O7Color and Shape:SolidMolecular weight:929.24Hinnuliquinone
CAS:Hinnuliquinone is an anti-HIV agent.Formula:C32H30N2O4Purity:98%Color and Shape:SolidMolecular weight:506.59ICeD-2
ICeD-2 triggers death in HIV-1 infected cells, requires HIV protease, inhibits DPP8/9, and stabilizes DPP9 in PBMCs.Formula:C20H29N3OColor and Shape:SolidMolecular weight:327.46CI-39
CAS:CI-39, an NNRTI with EC50 of 3.40 µM, inhibits HIV-1 reverse transcriptase and RNase H, with CC50 >30 µM.Formula:C19H18N2O4Color and Shape:SolidMolecular weight:338.36HIV-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.Formula:C40H45N7O4Color and Shape:SolidMolecular weight:687.83Acetyl-pepstatin
CAS:Streptomyces pepsin inhibitor is used as a pepsin inhibitor.Formula:C31H57N5O9Color and Shape:SolidMolecular weight:643.81PROTAC 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.Color and Shape:Odour SolidHIV-1 inhibitor-12
HIV-1 inhibitor-12: potent at inhibiting HIV-1 capsid protein polymerization with 9 nM IC50.Formula:C42H36ClF10N7O5S2Color and Shape:SolidMolecular weight:1008.35N36Mut(e,g)
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.Formula:C189H317N55O56Color and Shape:SolidMolecular weight:4255.87Indoline
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.Formula:C8H9NColor and Shape:Clear To Yellow LiquidMolecular weight:119.16Carbovir triphosphate
CAS:Carbovir triphosphate (CBV-TP), a phosphorylated metabolite, serves as a research tool for studying human immunodeficiency virus (HIV) [1].Formula:C11H16N5O11P3Color and Shape:SolidMolecular weight:487.19Decanoyl-RVKR-CMK
CAS:Inhibits all seven proprotein convertases; stops proET-1 processing; hinders VGF secretion in PC12 cells.Formula:C34H66ClN11O5Purity:98%Color and Shape:SolidMolecular weight:744.42Morin 3-O-β-D-glucopyranoside
CAS:Morin 3-O-β-D-glucopyranoside, a natural flavonoid, exhibits antifungal, anticancer, and antioxidant properties.Formula:C21H20O12Color and Shape:SolidMolecular weight:464.38Amdoxovir
CAS:Amdoxovir is a reverse transcriptase inhibitor.Formula:C9H12N6O3Color and Shape:SolidMolecular weight:252.23GLR-19
CAS:GLR-19 is an anti-HIV peptide with demonstrated antiviral activity against HSV-2 [1] [2].Formula:C102H194N40O20Purity:98%Color and Shape:SolidMolecular weight:2300.89HIV-1 inhibitor-59
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.Formula:C28H28FN5O3SColor and Shape:SolidMolecular weight:533.62SDZ 283-910
CAS:SDZ 283-910 is used as a statine-derived inhibitor.Formula:C46H59N5O9Purity:98%Color and Shape:SolidMolecular weight:826.004HIV-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-typeFormula:C26H24N6O2Color and Shape:SolidMolecular weight:452.51Ditiocarb
CAS:Ditiocarb speeds up copper cementation, cuts HIV risk, and boosts high-risk breast cancer immunoresearch.Formula:C5H11NS2Color and Shape:SolidMolecular weight:149.28Delavirdine
CAS:Delavirdine, an NNRTI for HIV-1, is used in HAART.
Formula:C22H28N6O3SColor and Shape:SolidMolecular weight:456.56Emtricitabine S-oxide
CAS:Emtricitabine treats HIV; its degradation byproduct is Emtricitabine S-oxide.Formula:C8H10FN3O4SPurity:98%Color and Shape:SolidMolecular weight:263.25Salvianan A
CAS: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].Formula:C20H17NO2Color and Shape:SolidMolecular weight:303.35Cys-TAT(47-57)
CAS:Cys-TAT(47-57): arginine-rich peptide from HIV-1 TAT protein's transduction domain.Formula:C67H124N34O14SPurity:98%Color and Shape:SolidMolecular weight:1661.9912-Oxocalanolide A
12-Oxocalanolide A is a useful organic compound for research related to life sciences and the catalog number is T125675.Formula:C22H24O5Color and Shape:SolidMolecular weight:368.429HIV-1 protease-IN-10
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) andFormula:C23H40O5Purity:98%Color and Shape:SolidMolecular weight:396.56KRL74
CAS:KRL74 is a cyclic peptide inhibitor that interferes with the interaction between the p6 domain of the HIV Gag protein and the UEV domain of the human TSG101 protein (p6/UEV), with an IC50 of 5.44 μM and a Kd of 11.9 μM. It also inhibits the budding of HIV from host cells, exhibiting an IC50 of 2 μM in virus-like particle (VLP) budding assays.Formula:C50H61ClN10O9Color and Shape:SolidMolecular weight:981.53HIV 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 (AMQMLKETIFormula:C45H81N11O14S2Purity:98%Color and Shape:SolidMolecular weight:1064.32CTP518
CAS:CTP518, a deuterated Atazanivir derivative, is a HIV protease inhibitor.Formula:C38H52N6O7Purity:98%Color and Shape:SolidMolecular weight:719.95Kuguacin N
Kuguacin N is a useful organic compound for research related to life sciences and the catalog number is T126345.Formula:C30H46O4Color and Shape:SolidMolecular weight:470.694HIV-1 inhibitor-11
HIV-1 inhibitor-11, a fused pyridine ring derivative, is a HIV-1 inhibitor.Formula:C42H36ClF10N7O5S2Color and Shape:SolidMolecular weight:1008.35Peptide T TFA
CAS:Peptide T (TFA), an octapeptide from HIV-1 gp120, inhibits HIV binding to CD4.Formula:C37H56F3N9O18Purity:98%Color and Shape:SolidMolecular weight:971.89HIV-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.Formula:C32H44N2O8SColor and Shape:SolidMolecular weight:616.77(+)-Carbovir triphosphate
CAS:(+)-Carbovir triphosphate, Abacavir's active metabolite, studied for HIV-1 resistance and inhibition mechanisms.Formula:C11H16N5O11P3Color and Shape:SolidMolecular weight:487.19QYL-685
CAS:QYL-685 is a methylenecyclopropane nucleoside analog.Formula:C20H24N7O5PColor and Shape:SolidMolecular weight:473.42HIV-IN-2
CAS:HIV-IN-2 (Compound 100) is a potent inhibitor of HIV, showing potential for research into HIV infection [1].Formula:C34H27ClF7N9O3SColor and Shape:SolidMolecular weight:810.14Globotriaosylceramides (porcine)
CAS:Globotriaosylceramides, cell membrane glycosphingolipids, act as Shiga toxin receptors and accumulate in Fabry disease, resisting HIV by blocking gp120.Formula:C60H113NO18Color and Shape:SolidMolecular weight:1136.553Scirpusin A
CAS:Scirpusin A is a hydroxystilbene dimer from the rhizome of Scirpus fluviatilis and Xinjiang wine grape.Formula:C28H22O7Color and Shape:SolidMolecular weight:470.47L 754394
CAS:L 754394 is an effective and specific inhibitor of the HIV-1 protease.Formula:C38H47N5O5Color and Shape:SolidMolecular weight:653.81

