Determine the necessary mass, volume, or concentration for preparing a solution.
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Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Ritonavir is an antiretroviral (HIV) drug which inhibits a particular liver enzyme that normally metabolizes protease inhibitors, cytochrome P450-3A4 (CYP3A4).
Application:
Ritonavir has been used:
as a human immunodeficiency virus (HIV) protease inhibitor to study its effects on placental endocrine function
as an HIV protease inhibitor to study its effects on reduction of tetrazolium dye in human embryonic kidney cells
as an organic anion transporting polypeptide (OATP) inhibitor to study its effect on hepatic uptake of bergapten and imperatorin
| ALogP | 6 |
|---|
| Pubchem Sid | 504758621 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504758621 |
| Canonical Smiles | CC(C)C1=NC(=CS1)CN(C)C(=O)NC(C(C)C)C(=O)NC(CC2=CC=CC=C2)CC(C(CC3=CC=CC=C3)NC(=O)OCC4=CN=CS4)O |
| IUPAC Name | 1,3-thiazol-5-ylmethyl N-[(2S,3S,5S)-3-hydroxy-5-[[(2S)-3-methyl-2-[[methyl-[(2-propan-2-yl-1,3-thiazol-4-yl)methyl]carbamoyl]amino]butanoyl]amino]-1,6-diphenylhexan-2-yl]carbamate |
| InChIKey | NCDNCNXCDXHOMX-XGKFQTDJSA-N |
| INCHI | 1S/C37H48N6O5S2/c1-24(2)33(42-36(46)43(5)20-29-22-49-35(40-29)25(3)4)34(45)39-28(16-26-12-8-6-9-13-26)18-32(44)31(17-27-14-10-7-11-15-27)41-37(47)48-21-30-19-38-23-50-30/h6-15,19,22-25,28,31-33,44H,16-18,20-21H2,1-5H3,(H,39,45)(H,41,47)(H,42,46)/t28-,31-,32-,33-/m0/s1 |
| Isomeric SMILES | CC(C)C1=NC(=CS1)CN(C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC2=CC=CC=C2)C[C@@H]([C@H](CC3=CC=CC=C3)NC(=O)OCC4=CN=CS4)O |
| WGK Germany | 3 |
| RTECS | XA5310000 |
| Molecular Weight | 720.94 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives |
| Direct Parent | N-carbamoyl-alpha amino acids and derivatives |
| Alternative Parents | Valine and derivatives Alpha amino acid amides Amphetamines and derivatives 2,4-disubstituted thiazoles N-acyl amines Carbamate esters Heteroaromatic compounds Secondary carboxylic acid amides Ureas Secondary alcohols Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Organonitrogen compounds |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Valine or derivatives - N-carbamoyl-alpha-amino acid or derivatives - Alpha-amino acid amide - Amphetamine or derivatives - 2,4-disubstituted 1,3-thiazole - Monocyclic benzene moiety - Fatty amide - Fatty acyl - N-acyl-amine - Benzenoid - Azole - Heteroaromatic compound - Carbamic acid ester - Thiazole - Carboxamide group - Urea - Carbonic acid derivative - Secondary alcohol - Secondary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Alcohol - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as n-carbamoyl-alpha amino acids and derivatives. These are compounds containing an alpha amino acid (or a derivative thereof) which bears an carbamoyl group at its terminal nitrogen atom. |
| External Descriptors | carbamate ester - ureas - 1,3-thiazole - carboxamide - L-valine derivative |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Mar 11, 2026 | R126586 | |
| Certificate of Analysis | Mar 11, 2026 | R126586 | |
| Certificate of Analysis | Mar 11, 2026 | R126586 | |
| Certificate of Analysis | Mar 11, 2026 | R126586 | |
| Certificate of Analysis | Mar 11, 2026 | R126586 | |
| Certificate of Analysis | Mar 03, 2026 | R126586 | |
| Certificate of Analysis | Mar 03, 2026 | R126586 | |
| Certificate of Analysis | Aug 27, 2025 | R126586 | |
| Certificate of Analysis | Aug 27, 2025 | R126586 | |
| Certificate of Analysis | Oct 17, 2024 | R126586 | |
| Certificate of Analysis | Jun 20, 2024 | R126586 | |
| Certificate of Analysis | Jun 20, 2024 | R126586 |
| Solubility | Solvent:DMSO, Max Conc. mg/mL: 14.42, Max Conc. mM: 20 with gentle warming; Solvent:ethanol, Max Conc. mg/mL: 7.21, Max Conc. mM: 10 |
|---|---|
| Melt Point(°C) | 125 °C |
| Molecular Weight | 720.900 g/mol |
| XLogP3 | 6.000 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 18 |
| Exact Mass | 720.313 Da |
| Monoisotopic Mass | 720.313 Da |
| Topological Polar Surface Area | 202.000 Ų |
| Heavy Atom Count | 50 |
| Formal Charge | 0 |
| Complexity | 1040.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Han Xie, Li Song, Sagie Katz, Jinyu Zhu, Yawen Liu, Jinping Tang, Linjun Cai, Peter Hildebrandt, Xiao Xia Han. (2022) Electron transfer between cytochrome c and microsomal monooxygenase generates reactive oxygen species that accelerates apoptosis. Redox Biology, [PMID:35609401] [10.1016/j.redox.2022.102340] |
| 2. Qing Shen, Huijuan Yang, Yunyan Li, Shiyan Li, Kang Chen, Honghai Wang, Haixing Wang, Jianfeng Ma. (2022) Rapid determination of antiviral drugs in yellow catfish (Pelteobagrus fulvidraco) using graphene/silica nanospheres (G/KCC-1) based pipette tip solid-phase extraction with ultra-performance liquid chromatography-tandem mass spectrometry. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, [PMID:35007897] [10.1016/j.jchromb.2022.123097] |
| 3. Dai Tianming, Wang Min, Wang Pengzhen, Dai Libing, Dai Renke, Meng Qingqi. (2021) Inhibition effects of eight anti-coronavirus drugs on glycosides metabolism and glycosidases in human gut microflora. PHARMAZIE, 76 (5): (195-201). [PMID:33964992] [10.1691/ph.2021.01005] |
| 4. Ma Zhiyuan, Bai Mengru, Shen Shuying, Zhou Junshan, Dong Rong, Zhang Jiangjun, Weng Yayun, Li Li, Li Yongchen, Liu Dan, Yan Wei, Lin Nengming, Xia Jianmei. (2025) Real-world Plasma Exposure of Nirmatrelvir/Ritonavir in Chinese Hospitalized Patients With COVID-19: A Multicenter Retrospective Study. THERAPEUTIC DRUG MONITORING, [PMID:39882748] [10.1097/FTD.0000000000001305] |
| 5. Lingzhu Zhao, Siduo Xu, Shouhan Yao, Zhiqiang Wei, Guohua Lou, Jinjin Qi, Haofeng Xu, Xueyu Wang, Zhenggang Yang, Min Zheng. (2026) GLS4 Induces the Interferon Signaling Pathway During Hepatitis B Virus (HBV) Infection. JOURNAL OF MEDICAL VIROLOGY, 98 (1): (e70777). [PMID:41480806] [10.1002/jmv.70777] |
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