Mannan from Carob seed - ≥98% , CAS No.9036-88-8

CAS: 9036-88-8 Cat. No.: M490020

GRADE & PURITY ≥98%

Synonyms

EX-A8013M | Mannoglycan | (2S,3S,4S,5S,6R)-2-[(2R,3S,4R,5R,6S)-6-[(2R,3S,4R,5S,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2R,3R,4R,5S,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymeth

Storage

Store at 2-8°C

Shipped In

Wet ice

Overview

Monosaccharides (%)：Mannose: Galactose: Other sugars = 98: 1: 1

Main Chain Glycosidic Linkage：β-1,4

Substrate For (Enzyme)：endo-1,4-β-Mannanase

High purity Mannan (1,4-β-D-Mannan) for use in research, biochemical enzyme assays and analytical testing applications.

Prepared by controlled hydrolysis of carob galactomannan with β-mannanase and α-galactosidase. An excellent substrate for endo-1,4-β-D-mannanase.

Specifications

Synonyms

EX-A8013M | Mannoglycan | (2S, 3S, 4S, 5S, 6R)-2-[(2R, 3S, 4R, 5R, 6S)-6-[(2R, 3S, 4R, 5S, 6S)-4, 5-dihydroxy-2-(hydroxymethyl)-6-[(2R, 3R, 4R, 5S, 6R)-4, 5, 6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4, 5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymeth

Specifications & Purity

≥98%

Biochemical and Physiological Mechanisms

Mannan exhibits several biological properties, including antiproliferative, antioxidant, and immunomodulatory. It is used as a hardener ingredient and as an emulsion stabilizer. Mannan is also involved in the inhibition of pathogen adherence, regulation o

Storage

Store at 2-8°C

Shipped In

Wet ice

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

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 508814811
• Canonical Smiles: C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)OC4C(OC(C(C4O)O)O)CO)CO)CO)O)O)O)O
• IUPAC Name: (2S,3S,4S,5S,6R)-2-[(2R,3S,4R,5R,6S)-6-[(2R,3S,4R,5S,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2R,3R,4R,5S,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
• InChIKey: LUEWUZLMQUOBSB-GFVSVBBRSA-N
• INCHI: 1S/C24H42O21/c25-1-5-9(29)10(30)15(35)22(40-5)44-19-7(3-27)42-24(17(37)12(19)32)45-20-8(4-28)41-23(16(36)13(20)33)43-18-6(2-26)39-21(38)14(34)11(18)31/h5-38H,1-4H2/t5-,6-,7-,8-,9-,10+,11-,12-,13-,14+,15+,16+,17-,18+,19-,20-,21-,22+,23+,24+/m1/s1
• Isomeric SMILES: C([C@@H]1[C@H]([C@@H]([C@@H]([C@@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O)O)O[C@@H]3[C@H](O[C@H]([C@H]([C@H]3O)O)O[C@H]4[C@H](O[C@H]([C@H]([C@H]4O)O)O)CO)CO)CO)O)O)O)O
• WGK Germany: 3
• RTECS: OP1949500
• Reaxy-Rn: 25844083
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=25844083&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Oligosaccharides
• Alternative Parents: O-glycosyl compounds Oxanes Secondary alcohols Hemiacetals Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Oligosaccharide - O-glycosyl compound - Glycosyl compound - Oxane - Secondary alcohol - Hemiacetal - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.
• External Descriptors: Not available

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

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Insoluble in water. Can be dissolved at 20 mg/mL in 5% w/v sodium hydroxide.On neutralisation with 50% acetic acid, the mannan precipitates from solution as a very fine colloidal suspension. The suspension should be mixed gently by swirling the container
• Sensitivity: Moisture sensitive.
• Specific Rotation[α]: 89 °

References

1. Xuelian Zhou, Xuefeng Chen, Li Zhang, Jinna Yuan, Hu Lin, Mingqiang Zhu, Xiaoqin Xu, Guanping Dong, Junfen Fu, Wei Wu.  (2023)  Mannose-Binding Lectin Reduces Oxidized Low-Density Lipoprotein Induced Vascular Endothelial Cells Injury by Inhibiting LOX1-ox-LDL Binding and Modulating Autophagy.  Biomedicines,  11  (6): (1743).  [PMID:37371838] [10.3390/biomedicines11061743]

2. Qin-wen Gao, Wei-ying Liu, Mirza Jawad, Lei Ci, Yi-yi Cao, Jing Xi, Jia-ying Wu, Yu-yang Lei, Yu-shi Hu, Xin-yue You, Xin-yu Zhang, Jian Fei, Yang Luan.  (2025)  Aristolochic acid IVa ameliorates arthritis in SKG Mice by regulating macrophage polarization and Th17/Treg balance.  PHYTOMEDICINE,      [PMID:40043543] [10.1016/j.phymed.2025.156557]

3. Qian Zhong, Xiaolong Shi, Yu Song, Peng Lei, Xiaoqi Xu, Hong Xu, Yibin Qiu, Sha Li.  (2024)  De novo synthesis of hyaluronic acid with tailored molecular weights using a new hyaluronidase SthHL.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39743112] [10.1016/j.ijbiomac.2024.139381]

4. Meng Li, Biwen Yang, Jiayi Tang, Mengling Ning, Zerong Guan, Zhenzhen Li, Binggang Ye, Huiqing Zhong, Zhouyi Guo, Zhiming Liu.  (2024)  Dynamic visualization monitoring of cell membrane damage using polarity-responsive amphiphilic carbon dots.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.149038]

5. Taotao Zhou, Xin Ju, Lishi Yan, Ruiqi Fang, Xinqi Xu, Liangzhi Li.  (2024)  Production of mannooligosaccharides from orange peel waste with β-mannanase expressed in Trichosporonoides oedocephalis.  BIORESOURCE TECHNOLOGY,      [PMID:38278453] [10.1016/j.biortech.2024.130373]

6. Qingzhi Ding, Yuan Zheng, Yongqi Zhu, Huamin Yang, Lin Luo, Haile Ma, Xiaoran Li.  (2024)  Propolis extract and Hermetia illucens larval proteins synergistically inhibit the growth of Aspergillus niger.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2024.104661]

7. Pengwei Chen, Haotian Wu, Yajing Zhao, Lv Zhong, Yujiao Zhang, Xundi Zhan, Aoxiang Xiao, Yunyun Huang, Hong Zhang, Bai-Ou Guan.  (2024)  Quantitative Assessment of Fungal Biomarkers in Clinical Samples via an Interface-Modulated Optical Fiber Biosensor.  ADVANCED MATERIALS,      [PMID:38373270] [10.1002/adma.202312985]