Maltohexaose - 10mM in DMSO , CAS No.34620-77-4

CAS: 34620-77-4 Cat. No.: M423530 Formula: C₃₆H₆₂O₃₁ Peso molecolare: 990.86

GRADE & PURITY 10mM in DMSO

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Specifiche e purezza

10mM in DMSO

Condizioni di conservazione di stoccaggio

Store at -80°C

Spedito in

Dry ice packs + Cold packs

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Nomi e identificatori

• Pubchem Sid: 528776673
• Sorrisi canonici: C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)OC4C(OC(C(C4O)O)OC5C(OC(C(C5O)O)OC6C(OC(C(C6O)O)O)CO)CO)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)-6-[(2R,3S,4R,5R,6R)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2R,3S,4R,5R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
• InChIKey: OCIBBXPLUVYKCH-LIGGPISVSA-N
• INCHI: 1S/C36H62O31/c37-1-7-13(43)14(44)21(51)32(58-7)64-27-9(3-39)60-34(23(53)16(27)46)66-29-11(5-41)62-36(25(55)18(29)48)67-30-12(6-42)61-35(24(54)19(30)49)65-28-10(4-40)59-33(22(52)17(28)47)63-26-8(2-38)57-31(56)20(50)15(26)45/h7-56H,1-6H2/t7-,8-,9-,10-,11-,12-,13-,14+,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31?,32-,33-,34-,35-,36-/m1/s1
• Isomeri 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[C@@H]5[C@H](O[C@@H]([C@@H]([C@H]5O)O)O[C@@H]6[C@H](OC([C@@H]([C@H]6O)O)O)CO)CO)CO)CO)CO)O)O)O)O
• Peso molecolare: 990.86
• Reaxy-Rn: 25970419
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=25970419&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: 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
• Descrizione: 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

Proprietà chimiche e fisiche

• Sensibilità: Moisture sensitive
• Peso molecolare: 990.900 g/mol
• XLogP3: -13.300
• Hydrogen Bond Donor Count: 20
• Hydrogen Bond Acceptor Count: 31
• Rotatable Bond Count: 16
• Exact Mass: 990.328 Da
• Monoisotopic Mass: 990.328 Da
• Topological Polar Surface Area: 506.000 Ų
• Heavy Atom Count: 67
• Formal Charge: 0
• Complexity: 1510.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 29
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Riferimenti

1. HuaYang Si, Yimeng Chen, Jie Yang, Xiaodong Wen.  (2023)  Characterization and comparison of polysaccharides from Achyranthes bidentata, Cyathula officinalis and Achyranthes aspera by saccharides mapping.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:36739718] [10.1016/j.jpba.2023.115272]

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. Yu Lu, Cheng Li, Jie Liu, Wenqi Huang, Yuerong Yang, Yue Jia, Tingting Liu, Linjuan Huang, Zhongfu Wang.  (2020)  Alteration of the goat milk glycoproteins N/O-glycome at different lactation stages.  FOOD CHEMISTRY,      [PMID:33092920] [10.1016/j.foodchem.2020.128221]

4. 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]

5. 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]

6. 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]

7. 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]

8. Huang Haidong, Li Yangyang, Song Jinsong, Zhao Yuhan, Liu Yanfeng, Li Jianghua, Du Guocheng, Chen Jian, Li Zhendong, Lv Xueqin, Xu Xianhao, Liu Long.  (2026)  Computationally Guided Engineering of Multi-Enzyme Cascades Enables Efficient Trehalose Biosynthesis.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  74  (30): (23649-23661).  [PMID:42554812] [10.1021/acs.jafc.6c05712]