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製品番号: HY-114184

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MK-8245 analog

Name: MK-8245 analog
Brand: MedChemExpress
SKU: HY-114184
Price: 215.00 USD
Availability: InStock
Rating: 5 (1 reviews)

MK-8245 analog (compound 6) is a potent stearoyl-CoA desaturase (SCD) inhibitor with an IC₅₀ of 7 nM for rat SCD. MK-8245 analog has antidiabetic and antidyslipidemic effects.

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CAS 番号: 1030612-87-3
分子式: C₁₆H₁₅BrFN₇O₃S
分子量:484.30

保管条件:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (265 KB)

MK-8245 analog 構造式

CAS 番号: 1030612-87-3

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生物活性
- 製品説明
- IC₅₀ & Target
- Cellular Effect
化学情報
純度とドキュメンテーション
参考文献
Calculators
Help & FAQs
関連分類
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生物活性

製品説明

MK-8245 analog (compound 6) is a potent stearoyl-CoA desaturase (SCD) inhibitor with an IC₅₀ of 7 nM for rat SCD. MK-8245 analog has antidiabetic and antidyslipidemic effects^[1].

IC₅₀ & Target

IC₅₀: 7 nM (rat SCD)^[1]

Cellular Effect

Cell Line	Type	Value	Description	References
Hepatocyte	IC₅₀	189 nM Compound: 6	Inhibition of SCD-1 activity in Sprague-Dawley rat Hepatocytes expressing organic anion transporting polypeptides assessed as reduction in [I-14C] stearoyl CoA desaturation by scintillation counting Inhibition of SCD-1 activity in Sprague-Dawley rat Hepatocytes expressing organic anion transporting polypeptides assessed as reduction in [I-14C] stearoyl CoA desaturation by scintillation counting	[PMID: 21661758]
HepG2	IC₅₀	>100000 μM Compound: 6	Inhibition of human delta6 desaturase activity expressed in human HEpG2 cells Inhibition of human delta6 desaturase activity expressed in human HEpG2 cells	[PMID: 21661758]
HepG2	IC₅₀	>100000 μM Compound: 6	Inhibition of rat delta-5 desaturase activity expressed in human HEpG2 cells Inhibition of rat delta-5 desaturase activity expressed in human HEpG2 cells	[PMID: 21661758]
HepG2	IC₅₀	>100000 μM Compound: 6	Inhibition of rat delta-6 desaturase activity expressed in human HEpG2 cells Inhibition of rat delta-6 desaturase activity expressed in human HEpG2 cells	[PMID: 21661758]
HepG2	IC₅₀	904 nM Compound: 6	Inhibition of SCD-1 activity in organic anion transporting polypeptides-deficient human HepG2 cells assessed as reduction in [I-14C] stearoyl CoA desaturation by scintillation counting Inhibition of SCD-1 activity in organic anion transporting polypeptides-deficient human HepG2 cells assessed as reduction in [I-14C] stearoyl CoA desaturation by scintillation counting	[PMID: 21661758]
HepG2	IC₅₀	>100000 μM Compound: 6	Inhibition of human delta-5 desaturase activity expressed in human HEpG2 cells Inhibition of human delta-5 desaturase activity expressed in human HEpG2 cells	[PMID: 21661758]

化学情報

CAS 番号 1030612-87-3
分子量 484.30
分子式 C₁₆H₁₅BrFN₇O₃S
SMILES

O=C(O)CN1N=C(C2=NN=C(N3CCC(OC4=CC(F)=CC=C4Br)CC3)S2)N=N1
輸送条件

Room temperature in continental US; may vary elsewhere.
保管条件

Please store the product under the recommended conditions in the Certificate of Analysis.

純度とドキュメンテーション

バッチを選択:

純度: 99.98%

Assay: 99.98%

ee.: 99.98%

データシート (265 KB)
COA (2659 KB)
元素分析報告書 (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
取扱説明書 (2659 KB)

参考文献

[1]. Renata M Oballa, et al. Development of a liver-targeted stearoyl-CoA desaturase (SCD) inhibitor (MK-8245) to establish a therapeutic window for the treatment of diabetes and dyslipidemia. J Med Chem. 2011 Jul 28;54(14):5082-96. [Content Brief]

Calculators

モル濃度計算機

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

濃度濃度

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分子量分子量

希釈計算機

濃度 _(開始) × 体積 _(開始) = 濃度 _(終了) × 体積 _(終了)

濃度 _(開始) 濃度 _(開始)

体積 _(開始) 体積 _(開始)

濃度 _(終了) 濃度 _(終了)

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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100 mg

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