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.
Lagerung bei 2-8°C Ships Nasses Eis 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 ist ein antiretrovirales (HIV-)Medikament, das ein bestimmtes Leberenzym hemmt, das normalerweise Proteaseinhibitoren metabolisiert, nämlich Cytochrom P450-3A4 (CYP3A4).
Anwendung:
Ritonavir wurde verwendet:
als Proteaseinhibitor des Humanen Immundefizienzvirus (HIV) zur Untersuchung seiner Auswirkungen auf die endokrine Funktion der Plazenta
als HIV-Proteaseinhibitor zur Untersuchung seiner Auswirkungen auf die Reduktion von Tetrazolium-Farbstoff in menschlichen embryonalen Nierenzellen
als Inhibitor des organischen anionentransportierenden Polypeptids (OATP) zur Untersuchung seiner Wirkung auf die hepatische Aufnahme von Bergapten und Imperatorin
| ALogP | 6 |
|---|
| Pubchem Sid | 504758621 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504758621 |
| Kanonisches Lächeln | 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 |
| Isomere 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 Deutschland | 3 |
| RTECS | XA5310000 |
| Molekulargewicht | 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 |
| Klasse | 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 |
| Beschreibung | 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 | Datum | Artikel |
|---|---|---|---|
| Certificate of Analysis | Jul 07, 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 | Aug 18, 2022 | R126586 | |
| Certificate of Analysis | Aug 18, 2022 | R126586 | |
| Certificate of Analysis | Aug 18, 2022 | R126586 | |
| Certificate of Analysis | Aug 18, 2022 | R126586 | |
| Certificate of Analysis | Aug 18, 2022 | R126586 | |
| Certificate of Analysis | Aug 18, 2022 | R126586 | |
| Certificate of Analysis | Aug 18, 2022 | R126586 |
| Löslichkeit | 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 |
|---|---|
| Schmelzpunkt (°C) | 125 °C |
| Molekulargewicht | 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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