Maltotetraose - Moligand™, ≥97% , CAS No.34612-38-9

CAS: 34612-38-9 Cat. No.: M121069 Molecular Weight: 666.58 Beilstein Registry Number: 78870 EC Number: 252-111-0

GRADE & PURITY Moligand™, ≥97%

Synonyms

Fujioligo 450 | α-1,4-Tetraglucose

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Overview

Maltotetraose(Fujioligo 450)   are potent inhibitors of TNF-α-induced intercellular adhesion molecule-1 (ICAM-1) expression, maltotetraose may be beneficial in the suppression of early atherosclerosis development.

Specifications

Synonyms

Fujioligo 450 | α-1, 4-Tetraglucose

Specifications & Purity

Moligand™, ≥97%

Storage

Protected from light, 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

Moligand™

Purity

≥97%

Names and Identifiers

• 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: (2R,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6S)-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-ZLBHSGTGSA-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
• Molecular Weight: 666.58
• Beilstein: 78870
• 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: maltotetraose tetrasaccharide

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

Chemical and Physical Properties

• Solubility: Methanol (Slightly, Heated), Water (Slightly, Heated, Sonicated)
• Sensitivity: Hygroscopic；Light sensitive
• Melt Point(°C): 209-211°C
• Molecular Weight: 666.600 g/mol
• XLogP3: -9.000
• Hydrogen Bond Donor Count: 14
• Hydrogen Bond Acceptor Count: 21
• Rotatable Bond Count: 10
• Exact Mass: 666.222 Da
• Monoisotopic Mass: 666.222 Da
• Topological Polar Surface Area: 348.000 Ų
• Heavy Atom Count: 45
• Formal Charge: 0
• Complexity: 918.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 20
• 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

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2. Na Zhang, Xin Huang, Yun-Long Guo, Hao Yue, Chang-Bao Chen, Shu-Ying Liu.  (2021)  Evaluation of storage period of fresh ginseng for quality improvement of dried and red processed varieties.  Journal of Ginseng Research,      [PMID:35509815] [10.1016/j.jgr.2021.06.007]

3. Miaomiao Li, Jinhua Du, Kaili Zhang.  (2020)  Profiling of carbohydrates in commercial beers and their influence on beer quality.  JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE,  100  (7): (3062-3070).  [PMID:32077484] [10.1002/jsfa.10337]

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6. Zhoukun Li, Jiale Wu, Biying Zhang, Fei Wang, Xianfeng Ye, Yan Huang, Qiang Huang, Zhongli Cui.  (2015)  AmyM, a Novel Maltohexaose-Forming α-Amylase from Corallococcus sp. Strain EGB.  APPLIED AND ENVIRONMENTAL MICROBIOLOGY,  81  (6):   [PMID:25576603] [10.1128/AEM.03934-14]

7. Yue Guo, Shenglin Sun, Mingfei Gu, Liyue Zhang, Li Cheng, Zhaofeng Li, Caiming Li, Xiaofeng Ban, Yan Hong, Zhengbiao Gu.  (2024)  Optimization and analysis of dual-enzymatic synthesis for the production of linear glucan.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:38211915] [10.1016/j.ijbiomac.2024.129299]

8. Xin Zheng, Yufang Ma, Xinge Cui, Yi Wang, Jingjing Jiang, Ting Liu, Zhijun Zhang, Mingsheng Ma, Xiaohong Han, Cai Tie.  (2025)  Development of derivatization-enhanced EIEIO-driven glycosidic linkage sequencing (DEED-GL-Seq) strategy and its application to glycogen-sourced oligosaccharides profiling.  CARBOHYDRATE POLYMERS,      [PMID:40733807] [10.1016/j.carbpol.2025.123877]

9. Baojie Zhu, Jing Zhao, Shaoping Li.  (2025)  Saccharide mapping apparatus for real-time PAGE detection of polysaccharides.  Journal of Advanced Research,      [PMID:40049513] [10.1016/j.jare.2025.03.006]

10. Xueting Zhang, Tong Ye, Yanli Zhang, Li Huang, Yimeng Song, Xucheng Zhang, Yinliang Zhang, Yazhong Xiao, Wei Fang.  (2026)  Bioinformatics-assisted mining and engineering of α-amylase for efficient hydrolysis of raw corn and microalgal starch.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41643977] [10.1016/j.ijbiomac.2026.150675]