Olumacostat glasaretil - ≥98% , Acetyl-CoA carboxylase inhibitor, CAS No.1261491-89-7, Acetyl-CoA carboxylase inhibitor

CAS: 1261491-89-7 Cat. No.: O647026 Molecular Weight: 481.62 EC Number: 814-666-2 PubChem CID: 89497391
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
Olumacostat glasaretil | HY-17641 | SCHEMBL14856848 | Olumacostat glasaretil [USAN] | 4W6JDK2PLY | 2-[(2-Ethoxy-2-oxoethyl)methylamino]-2-oxoethyl 5-(tetradecyloxy)-2-furancarboxylate | EX-A1319 | UNII-4W6JDK2PLY | AC-31463 | DRM01B | Q27260586 | AMY39954
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
Size
Status
Price
Qty
1mg
O647026-1mg
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$132.90
5mg
O647026-5mg
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$240.90
10mg
O647026-10mg
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$360.90
50mg
O647026-50mg
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$1,080.90
100mg
O647026-100mg
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$1,720.90
200mg
O647026-200mg
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$2,600.90
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Why this grade

≥98% 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

Olumacostat glasaretil (DRM01) is a small molecule inhibitor of acetyl coenzyme A carboxylase ( ACC ).

In Vitro

Acetyl coenzyme A carboxylase controls the first, rate limiting step in fatty acid biosynthesis. Olumacostat glasaretil inhibits de novo lipid synthesis in primary and transformed human sebocytes. At 3 μM, olumacostat glasaretil reduces fatty acid synthesis to at or below baseline levels. 14 C-acetate incorporation levels are 85%-90% lower for\nSEB-1 cultures treated with olumacostat glasaretil at 20 μM compared to control samples. At 3 μM, olumacostat glasaretil reduces sebocyte triacylglycerol, cholesteryl/wax ester, diacylglycerol, cholesterol and phospholipid levels from control values on average by approximately 86%, 57%, 51%, 39% and 37%, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Olumacostat glasaretil is a pro-drug of the ACC inhibitor 5-(tetradecyloxy)-2-furoic acid (TOFA) and is designed to enhance delivery in vivo . Topical application of olumacostat glasaretil but not TOFA significantly reduces hamster ear sebaceous gland size. HPLC analyses of hamster ear extracts shows that olumacostat glasaretil treatment increases ACC levels and the ratio of acetyl-CoA to free CoA in tested animals, indicating increased fatty acid oxidation. These changes are consistent with ACC inhibition. Matrix-assisted laser desorption/ionization (MALDI) imaging reveals that OG applied onto Yorkshire pig ears accumulates in sebaceous glands relative to the surrounding dermis . At week 12, OG treatment shows greater reductions from baseline in inflammatory lesions and noninflammatory lesions, and more patients with greater than or equal to 2-grade improvement in investigator global assessment score than vehicle. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

Specifications

Synonyms
Olumacostat glasaretil | HY-17641 | SCHEMBL14856848 | Olumacostat glasaretil [USAN] | 4W6JDK2PLY | 2-[(2-Ethoxy-2-oxoethyl)methylamino]-2-oxoethyl 5-(tetradecyloxy)-2-furancarboxylate | EX-A1319 | UNII-4W6JDK2PLY | AC-31463 | DRM01B | Q27260586 | AMY39954
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
Olumacostat glasaretil (DRM01) is a small molecule inhibitor of acetyl coenzyme A carboxylase ( ACC ).
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
Acetyl-CoA carboxylase inhibitor
Purity
≥98%
Product Properties
ALogP8
Names and Identifiers
Canonical SmilesCCCCCCCCCCCCCCOC1=CC=C(O1)C(=O)OCC(=O)N(C)CC(=O)OCC
IUPAC Name[2-[(2-ethoxy-2-oxoethyl)-methylamino]-2-oxoethyl] 5-tetradecoxyfuran-2-carboxylate
InChIKeyFYJLDICZGDFWKP-UHFFFAOYSA-N
INCHI1S/C26H43NO7/c1-4-6-7-8-9-10-11-12-13-14-15-16-19-32-25-18-17-22(34-25)26(30)33-21-23(28)27(3)20-24(29)31-5-2/h17-18H,4-16,19-21H2,1-3H3
Isomeric SMILES CCCCCCCCCCCCCCOC1=CC=C(O1)C(=O)OCC(=O)N(C)CC(=O)OCC
PubChem CID 89497391
Molecular Weight 481.62

Documentation

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ 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.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentAlpha amino acid esters
Alternative Parents Furoic acid esters  Alkyl aryl ethers  Tertiary carboxylic acid amides  Heteroaromatic compounds  Carboxylic acid esters  Oxacyclic compounds  Monocarboxylic acids and derivatives  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Alpha-amino acid ester - Furoic acid ester - Furoic acid or derivatives - Alkyl aryl ether - Heteroaromatic compound - Tertiary carboxylic acid amide - Furan - Carboxamide group - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Ether - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SolubilityDMSO : 125 mg/mL (259.54 mM; Need ultrasonic)
Molecular Weight481.600 g/mol
XLogP38.000
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count7
Rotatable Bond Count22
Exact Mass481.304 Da
Monoisotopic Mass481.304 Da
Topological Polar Surface Area95.300 Ų
Heavy Atom Count34
Formal Charge0
Complexity569.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
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