Curdlan - ≥80%, Derived from glucose fermentation , CAS No.54724-00-4

CAS: 54724-00-4 Cat. No.: C646156

GRADE & PURITY ≥80%, Derived from glucose fermentation

Synonyms

BDBM50240803 | glucoside | NCGC00263446-02 | (1->3)-beta-D-glucan | .beta.-D-Glucose | b-d-glucose | beta-D-glucose | GLUCOSE, .BETA.-D | CHEBI:37671 | YC46078 | (1->3)-beta-D-glucopyranan | Pharmakon1600-01300015 | Tabfine 097(HS) | DB02379 | (1->6)-beta

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Overview

Curdlan is a polysaccharide produced by bacteria and a homopolymer of glucose with β-1,3-glucosidic linkage.

Form:Solid

Specifications

Synonyms

BDBM50240803 | glucoside | NCGC00263446-02 | (1->3)-beta-D-glucan | .beta.-D-Glucose | b-d-glucose | beta-D-glucose | GLUCOSE, .BETA.-D | CHEBI:37671 | YC46078 | (1->3)-beta-D-glucopyranan | Pharmakon1600-01300015 | Tabfine 097(HS) | DB02379 | (1->6)-beta

Specifications & Purity

≥80%, Derived from glucose fermentation

Biochemical and Physiological Mechanisms

Curdlan is a polysaccharide produced by bacteria and a homopolymer of glucose with β-1, 3-glucosidic linkage.

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

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

Action Type

INHIBITOR

Purity

≥80%

Names and Identifiers

• Pubchem Sid: 528763947
• Canonical Smiles: C(C1C(C(C(C(O1)O)O)O)O)O
• IUPAC Name: (2R,3R,4S,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol
• InChIKey: WQZGKKKJIJFFOK-VFUOTHLCSA-N
• INCHI: 1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6-/m1/s1
• Isomeric SMILES: C([C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)O)O)O)O
• WGK Germany: 3
• Reaxy-Rn: 1907357
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1907357&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Monosaccharides
          • Level6 Hexoses

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Monosaccharides
• Direct Parent: Hexoses
• Alternative Parents: Oxanes Secondary alcohols Hemiacetals Polyols Oxacyclic compounds Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Hexose monosaccharide - Oxane - Secondary alcohol - Hemiacetal - Oxacycle - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.
• External Descriptors: D-glucopyranose

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

ASGR1 Tbio Asialoglycoprotein receptor 1 (30 Activities)

Discover Target: ASGR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

PC-12 (7051 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Solubility: DMSO : 10 mg/mL (Need ultrasonic) 0.1 M NaOH : 1 mg/mL (ultrasonic and adjust pH to 12 with NaOH)
• Sensitivity: Heat sensitive;Moisture sensitive
• Molecular Weight: 180.160 g/mol
• XLogP3: -2.600
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 180.063 Da
• Monoisotopic Mass: 180.063 Da
• Topological Polar Surface Area: 110.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 151.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 5
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Bingchao Duan, Yule He, Hongdan Hao, Lan Wang, Lingli Zhang, Yufei Wang, Congjun Liu, Yuling Li, Kui Lu, Xingzhao Yin, Chunyang Zhu, Liangqiu Huang, Yunyun Li, Yuhang Shen.  (2025)  Preparation of curdlan/tannin acid composite hydrogels with photothermal conversion, antibacterial and antioxidant properties.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2025.136402]

2. Xiaotong Zhang, Dongxue Wang, Chunyu Yang, Zhuoran Yang, Wei Guo.  (2025)  Konjac glucomannan-derived N-doped carbon aerogel for efficient solar-driven desalination and phenol degradation via advanced oxidation.  DESALINATION,      [PMID:] [10.1016/j.desal.2025.119520]