Olumacostat glasaretil

≥98%

Reagent Code: #62077
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CAS Number 1261491-89-7

science Other reagents with same CAS 1261491-89-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 481.62 g/mol
Formula C₂₆H₄₃NO₇
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Olumacostat glasaretil is a potent, selective inhibitor of acetyl-CoA carboxylase (ACC), a key enzyme in de novo fatty acid synthesis. It was investigated for the topical treatment of acne vulgaris. By inhibiting ACC in sebaceous glands, it reduces fatty acid production and sebum levels, a key factor in acne development. This mechanism showed efficacy against both inflammatory and non-inflammatory acne lesions in clinical studies. As a topical agent, it offers targeted action with minimal systemic exposure, limiting side effect risks. Development was discontinued after Phase 2 trials, and it is now available as a research chemical (≥98% purity).

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿6,768.00
inventory 5mg
10-20 days ฿12,312.00

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Olumacostat glasaretil
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Olumacostat glasaretil is a potent, selective inhibitor of acetyl-CoA carboxylase (ACC), a key enzyme in de novo fatty acid synthesis. It was investigated for the topical treatment of acne vulgaris. By inhibiting ACC in sebaceous glands, it reduces fatty acid production and sebum levels, a key factor in acne development. This mechanism showed efficacy against both inflammatory and non-inflammatory acne lesions in clinical studies. As a topical agent, it offers targeted action with minimal systemic exposu

Olumacostat glasaretil is a potent, selective inhibitor of acetyl-CoA carboxylase (ACC), a key enzyme in de novo fatty acid synthesis. It was investigated for the topical treatment of acne vulgaris. By inhibiting ACC in sebaceous glands, it reduces fatty acid production and sebum levels, a key factor in acne development. This mechanism showed efficacy against both inflammatory and non-inflammatory acne lesions in clinical studies. As a topical agent, it offers targeted action with minimal systemic exposure, limiting side effect risks. Development was discontinued after Phase 2 trials, and it is now available as a research chemical (≥98% purity).

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