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 EC Number: 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

Overview

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

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

Specifications & Purity

PharmPure™, USP

Biochemical and Physiological Mechanisms

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.

Storage

Store at -20°C, Argon charged

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

PharmPure™, USP

Action Type

ACTIVATOR

Mechanism of action

Activator of serpin family C member 1

Names and Identifiers

• Pubchem Sid: 504772286
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504772286
• Canonical 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+]
• 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
• Isomeric 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

Associated Targets(Human)

SERPINC1 Tclin Antithrombin-III (0 Activities)

Discover Target: SERPINC1

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

Chemical and Physical Properties

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

References

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]