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| Product | Description | |
|---|---|---|
| Amprenavir | Amprenavir. Group: Biochemicals. Alternative Names: N-[ (1S, 2R) -3-[[ (4-Aminophenyl) sulfonyl] (2-methylpropyl) amino]-2-hydroxy-1- (phenylmethyl) propyl]carbamic acid (3S)-tetrahydro-3-furanyl ester; 141W94; KVX-478. Grades: Highly Purified. CAS No. 161814-49-9. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C25H35N3O6S. US Biological Life Sciences. |  Worldwide |
| Amprenavir | Amprenavir promotes the specific interactions between the nuclear receptor pregnane X receptor (PXR) and the coactivators SRC-1 and PBP. Uses: Amprenavir is indicated in combination with other antiretroviral agents in the treatment of hiv-1 infection. Synonyms: VX-478; VX 478; VX478; Amprenavir; Agenerase; Prozei. Grades: >98%. CAS No. 161814-49-9. Molecular formula: C25H35N3O6S. Mole weight: 505.63. |  |
| Amprenavir | Amprenavir (VX-478) is a HIV protease inhibitor (Ki=0.6 nM) used to treat HIV infection. Amprenavir is also a SARS-CoV 3CL pro inhibitor with an IC 50 of 1.09 μM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: VX-478. CAS No. 161814-49-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17430. |  |
| Amprenavir (141W94, KVX-478, Agenerase, Prozei,) | Amprenavir (141W94, KVX-478, Agenerase, Prozei,). Group: Biochemicals. Alternative Names: 141W94, KVX-478, Agenerase, Prozei. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Amprenavir-d4 | Labeled Amprenavir, a selective HIV protease inhibitor. An analogue of Ritonavir. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Fosamprenavir | Fosamprenavir, also called as GW433908, Lexiva and Telzir, is an oral prodrug of the protease inhibitor (PI) amprenavir. Combined with other antiretroviral agents, Fosamprenavir is indicated for the treatment of patients with HIV infection, particularly those who have not previously received antiretroviral therapy. Synonyms: [(3S)-oxolan-3-yl] N-[(2S,3R)-4-[(4-aminophenyl)sulfonyl-(2-methylpropyl)amino]-1-phenyl-3-phosphonooxybutan-2-yl]carbamate; 3-(((4-aminophenyl)sulfonyl)(2-methylpropyl)amino)-1-(phenylmethyl)-2-(phosphonooxy)propyl)carbamic acid C-(tetrahydro-3-furanyl) ester; fosamprenavir; 226700-81-8 (calcium) GW 433908; GW-433908; GW-908. Grades: > 95%. CAS No. 226700-79-4. Molecular formula: C25H36N3O9PS. Mole weight: 585.62. | |
| Fosamprenavir | Fosamprenavir (Amprenavir phosphate;GW 433908) is a phosphate ester proagent of the antiretroviral protease inhibitor Amprenavir, with improved solubility [1]. Anti- HIV infection [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Amprenavir phosphate; GW 433908. CAS No. 226700-79-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg. Product ID: HY-78726. | |
| Fosamprenavir Calcium Salt | HIV protease inhibitor; water soluble prodrug of amprenavir. Synonyms: GW 433908G; Lexiva; GW433908G; GW-433908G. Grades: >98%. CAS No. 226700-81-8. Molecular formula: C25H34CaN3O9PS. Mole weight: 623.67. | |
| Fosamprenavir Calcium Salt (GW-433908G, Lexiva, Telzir) | HIV protease inhibitor; water soluble prodrug of amprenavir. Group: Biochemicals. Alternative Names: GW-433908G; Lexiva; Telzir. Grades: Highly Purified. CAS No. 226700-81-8. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Fosamprenavir-d4 | Fosamprenavir-d4 is deuterium labeled Fosamprenavir. Group: Isotope-labeled synthetic intermediates. Alternative Names: Amprenavir phosphate-d4; GW 433908-d4. CAS No. 1133702-41-6. Molecular formula: C25H32D4N3O9PS. Mole weight: 589.63. Canonical SMILES: O=C (O[C@H]1CCOC1)N[C@@H] (CC2=CC=CC=C2)[C@H] (OP (O) (O)=O)CN (CC (C)C)S (=O) (C3=C ([2H])C ([2H])=C (C ([2H])=C3[2H])N)=O. Catalog: ACM1133702416. |  |
| Fosamprenavir-d4 Calcium Salt (GW-433908G-d4, Lexiva-d4, Telzir-d4) | HIV protease inhibitor; water soluble prodrug of amprenavir. Group: Biochemicals. Alternative Names: GW-433908G-d4; Lexiva-d4; Telzir-d4. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 1-epi-Darunavir | Stereoisomer to Darunavir (D193500), a second generation HIV-1-protease inhibitor; structurally similar to amprenavir. Antiviral. Group: Biochemicals. Alternative Names: [ (1R, 2R) -3-[[ (4-Aminophenyl) sulfonyl] (2-methylpropyl) amino]-2-hydroxy-1- (phenyl-methyl) propyl]carabamic Acid (3R,3aS,6aR)-Hexahydrofuro[2,3-b]-furan-3-yl Ester. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| (1R,2S)-Darunavir | 1R,2S)-Darunavir is a diastereomer of Darunavir (D193500), a second generation HIV-1-protease inhibitor; structurally similar to amprenavir. Antiviral. Group: Biochemicals. Grades: Highly Purified. CAS No. 1402142-63-5. Pack Sizes: 500ug, 5mg. Molecular Formula: C27H37N3O7S, Molecular Weight: 547.66. US Biological Life Sciences. | Worldwide |
| {[(1S,2R)-1-Benzyl-2-hydroxy-3-[isobutyl-(4-nitro-benzenesulfonyl)-amino]-propyl}-carbamic Acid, tert-butyl Ester | A intermediate in the synthesis of Amprenavir, a selective HIV protease inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| [ (1S, 2R) -1-Benzyl-2-hydroxy-3- [isobutyl-d9- [ (4-nitrophenyl) sulfonyl] amino] propyl] carbamic Acid tert-Butyl Ester | An intermediate in the synthesis of labeled Amprenavir, a selective HIV protease inhibitor. Group: Biochemicals. Alternative Names: N-[ (1S, 2R) -2-Hydroxy-3-[ (2-methylpropyl-d9) [ (4-nitrophenyl) sulfonyl]amino]-1- (phenylmethyl) propyl]carbamic Acid 1,1-Dimethylethyl Ester. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| [ (1S, 2R) -3-[[ (4-Nitrophenyl) sulfonyl] (2-methylpropyl) amino]-2-hydroxy-1-phenylmethyl) propyl]carbamic Acid, (3S)-Tetrahydro-3-furan-d4-yl Ester | A labeled intermediate in the synthesis of Amprenavir, a selective HIV protease inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| [ (1S, 2R) -3-[[ (4-Nitrophenyl) sulfonyl] (2-methylpropyl) amino]-2-hydroxy-1-phenylmethyl) propyl]carbamic Acid, (3S)-Tetrahydro-3-furanyl Ester | A intermediate in the synthesis of Amprenavir, a selective HIV protease inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 2,3-Dideoxy-4,5-O-(1-methylethylidene)-3-(nitromethyl)-L-threo-pentonic Acid Ethyl Ester | 2,3-Dideoxy-4,5-O-(1-methylethylidene)-3-(nitromethyl)-L-threo-pentonic Acid Ethyl Ester is an impurity in the synthesis of Darunavir (D193500). Darunavir is a second generation HIV-1-protease inhibitor, which is structurally similar to Amprenavir (A634400). Group: Biochemicals. Grades: Highly Purified. CAS No. 501921-23-9. Pack Sizes: 10mg, 50mg. Molecular Formula: C11H19NO6, Molecular Weight: 261.27. US Biological Life Sciences. | Worldwide |
| 2-epi-Darunavir | 2-epi-Darunavir is a stereoisomer to Darunavir (D193500), a second generation HIV-1-protease inhibitor; structurally similar to amprenavir. Antiviral. Group: Biochemicals. Grades: Highly Purified. CAS No. 850141-19-4. Pack Sizes: 1mg, 5mg. Molecular Formula: C27H37N3O7S. US Biological Life Sciences. | Worldwide |
| Atazanavir | Atazanavir is a novel and potent azapeptide protease inhibitor that specifically inhibits the human immunodeficiency virus type 1 (HIV-1) protease enzyme with inhibition constant Ki of 66 nmol/L and also inhibits the viral replication of HIV-1 with 50% effective concentration EC50 ranging from 2.6 to 5.3 nmol/L. Atazanavir binds to HIV-1 protease preventing the cleavage of gag and gag-pol polyproteins, which results in the formation of immature virions in HIV-1-infected cells. Atazanavir has a different C-2 symmetric chemical structure and a generally greater antiretroviral potency in various HIV strains compared to other protease inhibitors, including indinavir, nelfinavir, ritonavir, saquinavir and amprenavir. Synonyms: Atazanavir ; Reyataz ; Atazanavir sulfate ; CGP75136 ; CGP75176 ; CGP75355 ; BMS232632 ; CGP 73547 ; CGP 75136 ; CGP 75176 ; CGP 75355 ; CGP-73547 ; CGP-75136 ; CGP-75176 ; CGP-75355 ; BMS 232632 ; BMS-232632 ; BMS-232632-05 ; C413408. Grades: 0.98. CAS No. 198904-31-3. Molecular formula: C38H52N6O7. Mole weight: 704.869. | |
| Brecanavir | Brecanavir is a tyrosyl-based arylsulfonamide, high-affinity, protease inhibitor (PI) for the treatment of human immunodeficiency virus type-1. This compound potently inhibited HIV-1 in cell culture assays with 50% effective concentrations (EC(50)s) of 0.2 to 0.53 nM and was equally active against HIV strains utilizing either the CXCR4 or CCR5 coreceptor, as was found with other PIs. Brecanavir had a <5-fold increase in EC(50)s against 80% of patient isolates tested and had a greater mean in vitro potency than amprenavir, indinavir, lopinavir, atazanavir, tipranavir, and darunavir. Uses: Hiv-1 protease inhibitor. Synonyms: Brecanavir; UNII-E367I8C7FI; CHEMBL206031; GW-0385; GW-640385; GW-640385X; VX-385; GW0385; GW640385; GW640385X; VX385; GW 0385; GW 640385; GW 640385X; VX 385; [(3aS,4R,6aR)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-4-yl] N-[(2S,3R)-4-[1,3-benzodioxol-5-ylsulfonyl(2-methylpropyl)amino]-3-hydroxy-1-[4-[(2-methyl-1,3-thiazol-4-yl)methoxy]phenyl]butan-2-yl]carbamate. Grades: ≥98%. CAS No. 313682-08-5. Molecular formula: C33H41N3O10S2. Mole weight: 703.82. | |
| Darunavir ([ (1S, 2R) -3-[[ (4-Aminophenyl) sulfonyl] (2-methylpropyl) amino]-2-hydroxy-1- (phenyl-methyl) propyl]carabamic Acid (3R,3aS,6aR)-Hexahydrofuro[2,3-b]-furan-3-yl Ester, TMC-114, UIC-94017) | Second generation HIV-1-protease inhibitor; structurally similar to amprenavir. Antiviral. Group: Biochemicals. Alternative Names: [ (1S, 2R) -3-[[ (4-Aminophenyl) sulfonyl] (2-methylpropyl) amino]-2-hydroxy-1- (phenyl-methyl) propyl]carabamic Acid (3R,3aS,6aR)-Hexahydrofuro[2,3-b]-furan-3-yl Ester; TMC-114; UIC-94017. Grades: Highly Purified. CAS No. 206361-99-1. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Darunavir-d9 ([ (1S, 2R) -3-[[ (4-Aminophenyl) sulfonyl] (2-methylpropyl-d9) amino]-2-hydroxy-1- (phenyl-methyl) propyl]carabamic Acid (3R,3aS,6aR)-Hexahydrofuro[2,3-b]-furan-3-yl Ester, TMC-114-d9, UIC-94017-d9) | Second generation HIV-1-protease inhibitor; structurally similar to amprenavir. Antiviral. Group: Biochemicals. Alternative Names: [ (1S, 2R) -3-[[ (4-Aminophenyl) sulfonyl] (2-methylpropyl-d9) amino]-2-hydroxy-1- (phenyl-methyl) propyl]carabamic Acid (3R,3aS,6aR)-Hexahydrofuro[2,3-b]-furan-3-yl Ester; TMC-114-d9; UIC-94017-d9. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
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