Enoxaparin sodium - PharmPure™, USP , Activator of serpin family C member 1, CAS No.679809-58-6, Activator of serpin family C member 1

CAS: 679809-58-6 Cat. No.: E413286 Numéro CE: 696-630-4 PubChem CID: 72679307

GRADE & PURITY PharmPure™, USP

Synonyms

Enoxaparin sodium | B0046-068182 | tetrasodium;2-[5-acetamido-6-[4-[5-acetamido-6-[2-carboxylato-4,5-dihydroxy-6-[[3-hydroxy-4-(sulfonatoamino)-6,8-dioxabicyclo[3.2.1]octan-2-yl]oxy]oxan-3-yl]oxy-2-(hydroxymethyl)-4-methyloxan-3-yl]oxy-6-carboxylato-2,3-d

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Vue d’ensemble

Information

Enoxaparin sodium is a low-molecular-weight heparin used to prevent and treat deep vein thrombosis or pulmonary embolism. It binds to and accelerates the activity of antithrombin III.

Specifications

Synonymes

Enoxaparin sodium | B0046-068182 | tetrasodium;2-[5-acetamido-6-[4-[5-acetamido-6-[2-carboxylato-4,5-dihydroxy-6-[[3-hydroxy-4-(sulfonatoamino)-6,8-dioxabicyclo[3.2.1]octan-2-yl]oxy]oxan-3-yl]oxy-2-(hydroxymethyl)-4-methyloxan-3-yl]oxy-6-carboxylato-2,3-d

Spécifications et pureté

PharmPure™, USP

Mécanismes biochimiques et physiologiques

Enoxaparin sodium is a low-molecular-weight heparin used to prevent and treat deep vein thrombosis or pulmonary embolism. It binds to and accelerates the activity of antithrombin III.

Conditions de stockage de stockage

Store at -20°C,Argon charged

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

PharmPure™, USP

Type d'action

ACTIVATOR

Mécanisme d'action

Activator of serpin family C member 1

Noms et identifiants

• Pubchem Sid: 504772286
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504772286
• Sourires canoniques: CC1C(C(OC(C1OC2CC(C(C(C2O)O)OC3C(C(C(C(O3)COS(=O)(=O)O)OC4C(C(C=C(O4)C(=O)[O-])O)O)O)NC(=O)C)C(=O)[O-])CO)OC5C(C(C(OC5C(=O)[O-])OC6C7COC(O7)C(C6O)NS(=O)(=O)[O-])O)O)NC(=O)C.[Na+].[Na+].[Na+].[Na+]
• IUPAC Name: tetrasodium;2-[5-acetamido-6-[4-[5-acetamido-6-[2-carboxylato-4,5-dihydroxy-6-[[3-hydroxy-4-(sulfonatoamino)-6,8-dioxabicyclo[3.2.1]octan-2-yl]oxy]oxan-3-yl]oxy-2-(hydroxymethyl)-4-methyloxan-3-yl]oxy-6-carboxylato-2,3-dihydroxycyclohexyl]oxy-4-hydroxy-2-(sulfooxymethyl)oxan-3-yl]oxy-3,4-dihydroxy-3,4-dihydro-2H-pyran-6-carboxylate
• InChIKey: CIJQTPFWFXOSEO-UHFFFAOYSA-J
• INCHI: 1S/C42H63N3O35S2.4Na/c1-9-19(43-10(2)47)39(79-33-27(55)28(56)42(80-34(33)37(61)62)78-31-17-7-69-38(74-17)21(25(31)53)45-81(63,64)65)73-16(6-46)29(9)71-14-4-12(35(57)58)30(26(54)23(14)51)76-40-20(44-11(3)48)24(52)32(18(75-40)8-70-82(66,67)68)77-41-22(50)13(49)5-15(72-41)36(59)60;;;;/h5,9,12-14,16-34,38-42,45-46,49-56H,4,6-8H2,1-3H3,(H,43,47)(H,44,48)(H,57,58)(H,59,60)(H,61,62)(H,63,64,65)(H,66,67,68);;;;/q;4*+1/p-4
• Isomères SMILES: CC1C(C(OC(C1OC2CC(C(C(C2O)O)OC3C(C(C(C(O3)COS(=O)(=O)O)OC4C(C(C=C(O4)C(=O)[O-])O)O)O)NC(=O)C)C(=O)[O-])CO)OC5C(C(C(OC5C(=O)[O-])OC6C7COC(O7)C(C6O)NS(=O)(=O)[O-])O)O)NC(=O)C.[Na+].[Na+].[Na+].[Na+]
• PubChem CID: 72679307

Cibles associées (humaines)

SERPINC1 Tclin Antithrombin-III (0 Activities)

Discover Target: SERPINC1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Propriétés chimiques et physiques

• Solubilité: Solubility (25°C) In vitro Water: 100 mg/mL DMSO: Insoluble; Ethanol: Insoluble
• Point de fusion (°C): >191°C

Références

1. Liang Zhang, Rouying Cai, Yao Wang, Chenfang Miao, Menghan Zhang, Chen Zheng, Jianzhong Zhang, Zhengjun Huang, Shaohuang Weng.  (2024)  Effectively detect enoxaparin using polymyxin B as medium through fluorescent strategy based on carbon dots with antioxidant activity.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.112615]

2. Fanqi Kong, Hongyue Yu, Lifei Gao, Enyun Xing, Yan Yu, Xiaofei Sun, Wenxing Wang, Dongyuan Zhao, Xiaomin Li.  (2024)  Multifunctional Hierarchical Nanoplatform with Anisotropic Bimodal Mesopores for Effective Neural Circuit Reconstruction after Spinal Cord Injury.  ACS Nano,      [PMID:38717602] [10.1021/acsnano.4c03252]

3. Chenfang Miao, Menghan Zhang, Ying Zheng, Xiaoyan Lin, Shuangying Yang, Linlin Xu, Sitong Lu, Zhengjun Huang, Jianyong Huang, Yanjie Zheng, Shaohuang Weng.  (2025)  An effective fluorescence strategy based on xanthine oxidase catalysis and the carbon dots’ specific response to ·OH for aminophylline pharmacokinetic studies.  Materials Today Bio,      [PMID:40677407] [10.1016/j.mtbio.2025.102019]