Dolutegravir Sodium - ≥99% , Human immunodeficiency virus type 1 integrase inhibitor, CAS No.1051375-19-9, Human immunodeficiency virus type 1 integrase inhibitor

CAS: 1051375-19-9 Cat. No.: D275163 Molecular Weight: 441.36 EC Number: 812-620-6
AVAILABLE TO ORDER
GRADE & PURITY ≥99%
Synonyms
DOLUTEGRAVIR SODIUM SALT [MI] | Dolutegravir (sodium) | DOLUTEGRAVIR SODIUM COMPONENT OF TRIUMEQ | Dolutegravir sodium salt | Dolutegravir sodium [USAN] | DOLUTEGRAVIR SODIUM COMPONENT OF JULUCA | TIVICAY PD | Tivicay (TN) | HY-13238A | SODIUM (4R,12AS)-9
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Size
Status
Price
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5mg
D275163-5mg
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25mg
D275163-25mg
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50mg
D275163-50mg
2

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100mg
D275163-100mg
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Integrase inhibitors are a new class of antiretroviral drugs blocking the action of HIV integrase, which catalyses several key steps in the life cycle of the virus and is essential for insertion of the viral genome into the host cell DNA. GSK1349572 is a next-generation HIV integrase (IN) inhibitor.

In vitro: GSK1349572 is a two-metal-binding HIV integrase strand transfer inhibitor whose mechanism of action was established through resistance passage experiments, integrase enzyme assays, mechanistic cellular assays and activity against viral strains resistant to other classes of anti-HIV agents. In a variety of cellular antiviral assays, GSK1349572 inhibited HIV replication with subnanomolar or low-nanomolar potency and with a selectivity index of 9,400. The protein-adjusted half-maximal effective concentration extrapolated to 100% human serum was 38 nM .

In vivo: No animial in vivo data are available for GSK1349572 so far.

Clinical trial: GSK1349572 was effective when given once daily without a pharmacokinetic booster and was well tolerated at all assessed doses. These findings support the assessment of once daily 50 mg GSK1349572 in phase 3 trials.

Specifications

Synonyms
DOLUTEGRAVIR SODIUM SALT [MI] | Dolutegravir (sodium) | DOLUTEGRAVIR SODIUM COMPONENT OF TRIUMEQ | Dolutegravir sodium salt | Dolutegravir sodium [USAN] | DOLUTEGRAVIR SODIUM COMPONENT OF JULUCA | TIVICAY PD | Tivicay (TN) | HY-13238A | SODIUM (4R, 12AS)-9
Specifications & Purity
≥99%
Biochemical and Physiological Mechanisms
Dolutegravir Sodium is an HIV-1 integrase inhibitor with an IC 50 of 2.7nM. No effect on total viral DNA synthesis in infected cells but blocks the integration of viral DNA into host DNA.
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
INHIBITOR
Mechanism of action
Human immunodeficiency virus type 1 integrase inhibitor
Purity
≥99%
Names and Identifiers
Pubchem Sid504770687
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504770687
Canonical SmilesCC1CCOC2N1C(=O)C3=C(C(=O)C(=CN3C2)C(=O)NCC4=C(C=C(C=C4)F)F)[O-].[Na+]
IUPAC Namesodium;(3S,7R)-13-[(2,4-difluorophenyl)methylcarbamoyl]-7-methyl-9,12-dioxo-4-oxa-1,8-diazatricyclo[8.4.0.03,8]tetradeca-10,13-dien-11-olate
InChIKeyUGWJRRXTMKRYNK-VSLILLSYSA-M
INCHI1S/C20H19F2N3O5.Na/c1-10-4-5-30-15-9-24-8-13(17(26)18(27)16(24)20(29)25(10)15)19(28)23-7-11-2-3-12(21)6-14(11)22;/h2-3,6,8,10,15,27H,4-5,7,9H2,1H3,(H,23,28);/q;+1/p-1/t10-,15+;/m1./s1
Isomeric SMILES C[C@@H]1CCO[C@@H]2N1C(=O)C3=C(C(=O)C(=CN3C2)C(=O)NCC4=C(C=C(C=C4)F)F)[O-].[Na+]
Molecular Weight 441.36
Reaxy-Rn 45353610
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=45353610&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassPyridines and derivatives
SubclassPyridinecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentPyridinecarboxylic acids and derivatives
Alternative Parents 2-heteroaryl carboxamides  Pyridinolates  Fluorobenzenes  1,3-oxazinanes  Aryl fluorides  Vinylogous amides  Vinylogous acids  Tertiary carboxylic acid amides  Heteroaromatic compounds  Secondary carboxylic acid amides  Cyclic ketones  Lactams  Oxacyclic compounds  Azacyclic compounds  Organic metal halides  Organic sodium salts  Organic zwitterions  Organofluorides  Organopnictogen compounds  Hydrocarbon derivatives  Organic oxides  Organonitrogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Pyridine carboxylic acid or derivatives - 2-heteroaryl carboxamide - Pyridinolate - Fluorobenzene - Halobenzene - 1,3-oxazinane - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Oxazinane - Benzenoid - Heteroaromatic compound - Tertiary carboxylic acid amide - Vinylogous amide - Vinylogous acid - Carboxamide group - Lactam - Secondary carboxylic acid amide - Cyclic ketone - Organic alkali metal salt - Organic metal halide - Azacycle - Oxacycle - Carboxylic acid derivative - Organic salt - Organonitrogen compound - Organofluoride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic zwitterion - Organic sodium salt - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as pyridinecarboxylic acids and derivatives. These are compounds containing a pyridine ring bearing a carboxylic acid group or a derivative thereof.
External Descriptors organic sodium salt
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MOLT-4 (49676 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MT4 (17854 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-937 (7138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PBMC (10003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
pol Human immunodeficiency virus type 1 integrase (9041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Canis familiaris (36305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human immunodeficiency virus 1 (70413 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human immunodeficiency virus 2 (5592 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDCK (10148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cynomolgus monkey (4946 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeDateItem
F2523368Certificate of AnalysisApr 02, 2026 D275163
L2205192Certificate of AnalysisJan 05, 2026 D275163
L2205190Certificate of AnalysisDec 12, 2025 D275163
L2205191Certificate of AnalysisDec 12, 2025 D275163
L2205196Certificate of AnalysisOct 14, 2022 D275163
Chemical and Physical Properties
Solubility0.2mg/ml in DMSO.
SensitivityMoisture sensitive
Molecular Weight441.400 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count8
Rotatable Bond Count3
Exact Mass441.111 Da
Monoisotopic Mass441.111 Da
Topological Polar Surface Area102.000 Ų
Heavy Atom Count31
Formal Charge0
Complexity836.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Solution Calculators
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