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Firsocostat (GS-0976), 乙酰辅酶羧化酶 1 的异构调节剂;乙酰辅酶羧化酶 2 的异构调节剂

乙酰辅酶A羧化酶抑制剂
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货号 (SKU) 包装规格 是否现货 价格 数量
F414250-2mg
2mg 现货 Stock Image
F414250-5mg
5mg 现货 Stock Image
F414250-10mg
10mg 现货 Stock Image
F414250-25mg
25mg 现货 Stock Image
F414250-50mg
50mg 现货 Stock Image
F414250-100mg
100mg 现货 Stock Image

基本描述

别名 1,4-二氢-1-[(2R)-2-(2-甲氧基苯基)-2-[(四氢-2H-吡喃-4-基)氧基]乙基]-alpha,alpha,5-三甲基-6-(2-恶唑基)-2,4-二氧代噻吩并[2,3-d]嘧啶-3(2H)-乙酸 | 菲索科斯塔 (GS-0976)
英文别名 FIRSOCOSTAT [WHO-DD] | ND-630; NDI-010976; Firsocostat | FIRSOCOSTAT [INN] | BS-15388 | THIENO(2,3-D)PYRIMIDINE-3(2H)-ACETIC ACID, 1,4-DIHYDRO-1-((2R)-2-(2-METHOXYPHENYL)-2-((TETRAHYDRO-2H-PYRAN-4-YL)OXY)ETHYL)-.ALPHA.,.ALPHA.,5-TRIMETHYL-6-(2-OXAZOLYL)-2
规格或纯度 Moligand™, ≥98%
英文名称 Firsocostat (GS-0976)
生化机理 Firsocostat(GS-0976,NDI-010976,ND-630)是乙酰辅酶羧化酶(ACC)的可逆抑制剂,对 hACC1 和 hACC2 的 IC50 分别为 2.1 nM 和 6.1 nM。
储存温度 -20°C储存
运输条件 超低温冰袋运输
作用类型 变构调节剂
作用机制 乙酰辅酶羧化酶 1 的异构调节剂;乙酰辅酶羧化酶 2 的异构调节剂
产品介绍

Firsocostat (GS-0976, NDI-010976, ND-630)是acetyl CoA carboxylase (ACC)的一种可逆抑制剂,对hACC1和hACC2的IC50分别为2.1 nM,6.1 nM。

Information

Firsocostat (GS-0976) Firsocostat (GS-0976, NDI-010976, ND-630) is a reversible inhibitor of acetyl CoA carboxylase (ACC) with IC50s of 2.1 nM,6.1 nM for hACC1 and hACC2,respectively.


Targets

hACC1 (Cell-free assay); hACC2 (Cell-free assay) 2.1 nM; 6.1 nM


In vitro

When ND-630 and [14C]acetate were administered to Hep-G2 cells for 4 h, ND-630 inhibited FASyn with EC50 values of 66 nM in cells cultured in medium containing. When ND-630 and[14C]palmitate were administered to C2C12 cells for 6 h, ND-630 increased both the release of [14C]O2 and the production of[14C]acid-soluble material.


In vivo

When administered chronically to rats with diet-induced obesity, ND-630 reduces hepatic steatosis, improves insulin sensitivity, reduces weight gain without affecting food intake, and favorably affects dyslipidemia.

纯度 ≥98%

产品属性

ALogP 2.946
hba_count 8
Rotatable Bond 9

关联靶点(人)

ACACB Tchem 乙酰辅酶A羧化酶2(Acetyl-CoA carboxylase 2) (2 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
ACACA Tchem 乙酰辅酶A羧化酶1(Acetyl-CoA carboxylase 1) (3 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)

名称和识别符

PubChem SID 504772151
分子类型 小分子
IIUPAC Name 2-[1-[(2R)-2-(2-methoxyphenyl)-2-(oxan-4-yloxy)ethyl]-5-methyl-6-(1,3-oxazol-2-yl)-2,4-dioxothieno[2,3-d]pyrimidin-3-yl]-2-methylpropanoic acid
INCHI 1S/C28H31N3O8S/c1-16-21-24(32)31(28(2,3)26(33)34)27(35)30(25(21)40-22(16)23-29-11-14-38-23)15-20(39-17-9-12-37-13-10-17)18-7-5-6-8-19(18)36-4/h5-8,11,14,17,20H,9-10,12-13,15H2,1-4H3,(H,33,34)/t20-/m0/s1
InChi Key ZZWWXIBKLBMSCS-FQEVSTJZSA-N
Smiles CC1=C(SC2=C1C(=O)N(C(=O)N2CC(C3=CC=CC=C3OC)OC4CCOCC4)C(C)(C)C(=O)O)C5=NC=CO5
Isomeric SMILES CC1=C(SC2=C1C(=O)N(C(=O)N2C[C@@H](C3=CC=CC=C3OC)OC4CCOCC4)C(C)(C)C(=O)O)C5=NC=CO5
分子量 569.63
Reaxy-Rn 23529544
Reaxys-RN link address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=23529544&ln=

化学和物理性质

溶解性 Solubility (25°C) In vitro DMSO: 100 mg/mL (175.55 mM); Ethanol: 4 mg/mL (7.02 mM); Water: Insoluble;
DMSO(mg / mL) Max Solubility 100
DMSO(mM) Max Solubility 175.552551656338
Water(mg / mL) Max Solubility <1
分子量 569.600 g/mol
XLogP3 3.200
氢键供体数Hydrogen Bond Donor Count 1
氢键受体数Hydrogen Bond Acceptor Count 10
可旋转键计数Rotatable Bond Count 9
精确质量Exact Mass 569.183 Da
单同位素质量Monoisotopic Mass 569.183 Da
拓扑极表面积Topological Polar Surface Area 160.000 Ų
重原子数Heavy Atom Count 40
形式电荷Formal Charge 0
复杂度Complexity 947.000
同位素原子数Isotope Atom Count 0
定义的原子立体中心计数Defined Atom Stereocenter Count 1
未定义的原子立体中心计数Undefined Atom Stereocenter Count 0
定义的键立体中心计数Defined Bond Stereocenter Count 0
未定义的键立体中心计数Undefined Bond Stereocenter Count 0
所有立体化学键的总数The total count of all stereochemical bonds 0
共价键合单元计数Covalently-Bonded Unit Count 1

安全和危险性(GHS)

象形图 GHS07
信号词 警告
危险声明

H302: 吞食有害

H315: 引起皮肤刺激

H319: 引起严重眼睛刺激

H335: 可能引起呼吸道刺激

预防措施声明

P261: 避免吸入灰尘/烟雾/气体/雾/蒸汽/喷雾

P305+P351+P338: 如进入眼睛:用水小心冲洗几分钟。如戴隐形眼镜并可方便地取出,取出隐形眼镜。继续冲洗。

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批号(Lot Number) 证书类型 货号
K2223312 分析证书 F414250
K2223321 分析证书 F414250
K2223351 分析证书 F414250
K2223355 分析证书 F414250
K2223375 分析证书 F414250
K2223376 分析证书 F414250

引用文献

1. Harriman G, Greenwood J, Bhat S, Huang X, Wang R, Paul D, Tong L, Saha AK, Westlin WF, Kapeller R et al..  (2016)  Acetyl-CoA carboxylase inhibition by ND-630 reduces hepatic steatosis, improves insulin sensitivity, and modulates dyslipidemia in rats..  Proc Natl Acad Sci USA,  113  (13): (E1796-805).  [PMID:26976583]
2. Loomba R, Kayali Z, Noureddin M, Ruane P, Lawitz EJ, Bennett M, Wang L, Harting E, Tarrant JM, McColgan BJ et al..  (2018)  GS-0976 Reduces Hepatic Steatosis and Fibrosis Markers in Patients With Nonalcoholic Fatty Liver Disease..  Gastroenterology,  155  (5): (1463-1473.e6).  [PMID:30059671]
3. Alkhouri N, Lawitz E, Noureddin M, DeFronzo R, Shulman GI.  (2020)  GS-0976 (Firsocostat): an investigational liver-directed acetyl-CoA carboxylase (ACC) inhibitor for the treatment of non-alcoholic steatohepatitis (NASH)..  Expert Opin Investig Drugs,  29  (2): (135-141).  [PMID:31519114]
4. Alkhouri N.  (2020)  NASH and NAFLD: emerging drugs, therapeutic targets and translational and clinical challenges..  Expert Opin Investig Drugs,  29  (2): (87).  [PMID:31984804]
5. Matsumoto M, Yashiro H, Ogino H, Aoyama K, Nambu T, Nakamura S, Nishida M, Wang X, Erion DM, Kaneko M.  (2020)  Acetyl-CoA carboxylase 1 and 2 inhibition ameliorates steatosis and hepatic fibrosis in a MC4R knockout murine model of nonalcoholic steatohepatitis..  PLoS ONE,  15  (1): (e0228212).  [PMID:31990961] [10.1371/journal.pone.0228212]
6. Kayampilly P, Roeser N, Rajendiran TM, Pennathur S, Afshinnia F.  (2022)  Acetyl Co-A Carboxylase Inhibition Halts Hyperglycemia Induced Upregulation of De Novo Lipogenesis in Podocytes and Proximal Tubular Cells..  Metabolites,  12  (10): [PMID:36295842] [10.3390/metabo12100940]

溶液计算器