Shanghai Nianxing Industrial Co., Ltd
China
Product Name: Lopinavir-D8
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Purity: 98.0%
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1224729-35-4

1224729-35-4 structure

Name: Lopinavir-d8
Chemical Name: Lopinavir-d8
CAS Number: 1224729-35-4
Molecular Formula: C₃₇H₄₀D₈N₄O₅
Molecular Weight: 636.85
Catalog: Signaling Pathways Anti-infection HIV
Create Date: 2021-10-18 08:00:56
Modify Date: 2024-01-03 22:47:20
Lopinavir-d8 (ABT-378-d8) is the deuterium labeled Lopinavir. Lopinavir (ABT-378) is a highly potent, selective peptidomimetic inhibitor of the HIV-1 protease, with Kis of 1.3 to 3.6 pM for wild-type and mutant HIV protease. Lopinavir acts by arresting maturation of HIV-1 thereby blocking its infectivity[1][2]. Lopinavir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 14.2 μM[3].

Name	Lopinavir-d8

Description	Lopinavir-d8 (ABT-378-d8) is the deuterium labeled Lopinavir. Lopinavir (ABT-378) is a highly potent, selective peptidomimetic inhibitor of the HIV-1 protease, with Kis of 1.3 to 3.6 pM for wild-type and mutant HIV protease. Lopinavir acts by arresting maturation of HIV-1 thereby blocking its infectivity[1][2]. Lopinavir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 14.2 μM[3].
Related Catalog	Signaling Pathways >> Anti-infection >> HIV Research Areas >> Infection Signaling Pathways >> Anti-infection >> SARS-CoV Signaling Pathways >> Metabolic Enzyme/Protease >> HIV Protease
In Vitro	Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].
References	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [2]. Cvetkovic RS, et al. Lopinavir/ritonavir: a review of its use in the management of HIV infection. Drugs. 2003;63(8):769-802. [3]. Sham HL, et al. ABT-378, a highly potent inhibitor of the human immunodeficiency virus protease. Antimicrob Agents Chemother. 1998;42(12):3218-3224. [4]. Qi Sun, et al. Bardoxolone and bardoxolone methyl, two Nrf2 activators in clinical trials, inhibit SARS-CoV-2 replication and its 3C-like protease. Signal Transduct Target Ther. 2021 May 29;6(1):212.

Molecular Formula	C₃₇H₄₀D₈N₄O₅
Molecular Weight	636.85

Hazard Codes	Xi

1322625-54-6	1224729-35-4
192725-39-6	357275-54-8
192725-17-0	221553-72-6
1794760-48-7	1538624-35-9
1092804-88-0	35434-71-0
1412944-99-0	1158522-08-7
940364-43-2	134104-43-1
131615-57-1	6906-52-1
930439-75-1	2089705-42-8
2248392-12-1	1018584-77-4