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Small Molecules & Compound Libraries
Plantagoside - 10mM in DMSO, high purity , CAS No.78708-33-5

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Plantagoside - 10mM in DMSO, high purity , CAS No.78708-33-5

1 Citations

COA

Grade & Purity:

10mM in DMSO

Cas Number: 78708-33-5
Molecular Weight: 466.39
PubChem CID: 174157

In stock

Item Number

P425961

Grouped product items
SKU	Size	Availability	Price	Qty
P425961-1ml	1ml	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$241.90

Mannosidase Inhibitors

View related series

Compound libraries (12325)

Basic Description

Synonyms	Plantagoside \| 78708-33-5 \| FR4TR9587N \| 2'-O-beta-Glucopyranosyl-5,7,4',5'-tetrahydroxyflavanone \| 4H-1-Benzopyran-4-one, 2-(3-(beta-D-glucopyranosyloxy)-4,5-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-, (S)- \| UNII-FR4TR9587N \| CHEBI:81163 \| DTXSID20229256 \| HY-N1470 \| s3
Specifications & Purity	10mM in DMSO
Biochemical and Physiological Mechanisms	Plantagoside, a flavanone glucoside isolated from the seeds of Plantago asiatica, is a specific and non-competitive alpha-mannosidase inhibitor with IC50 of 5 μM.
Storage Temp	Store at -80°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Information Plantagoside Plantagoside, a flavanone glucoside isolated from the seeds of Plantago asiatica , is a specific and non-competitive alpha-mannosidase inhibitor with IC50 of 5 μM. Targets alpha-mannosidase (Cell-free assay) 5 μM

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Phenylpropanoids and polyketides
  - Class Flavonoids
    - Subclass Flavonoid glycosides

Kingdom	Organic compounds
Superclass	Phenylpropanoids and polyketides
Class	Flavonoids
Subclass	Flavonoid glycosides
Intermediate Tree Nodes	Not available
Direct Parent	Flavonoid O-glycosides
Alternative Parents	3'-hydroxyflavonoids 4'-hydroxyflavonoids 5-hydroxyflavonoids 7-hydroxyflavonoids Flavanones Phenolic glycosides Hexoses Chromones O-glycosyl compounds Aryl alkyl ketones Catechols Phenoxy compounds Phenol ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Oxanes Vinylogous acids Secondary alcohols Acetals Polyols Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Organic oxides
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Flavonoid o-glycoside - Flavonoid-3p-o-glycoside - 3'-hydroxyflavonoid - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Hydroxyflavonoid - Flavanone - Flavan - Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Chromone - 1-benzopyran - Chromane - Benzopyran - Phenoxy compound - Catechol - Aryl alkyl ketone - Aryl ketone - Phenol ether - Phenol - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Monosaccharide - Monocyclic benzene moiety - Oxane - Vinylogous acid - Ketone - Secondary alcohol - Organoheterocyclic compound - Polyol - Acetal - Ether - Oxacycle - Primary alcohol - Alcohol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as flavonoid o-glycosides. These are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.
External Descriptors	flavanones
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

Product Properties

ALogP	-0.04
HBD Count	8
Rotatable Bond	4

Names and Identifiers

IUPAC Name	(2S)-2-[3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one
INCHI	InChI=1S/C21H22O12/c22-6-15-18(28)19(29)20(30)21(33-15)32-14-2-7(1-11(26)17(14)27)12-5-10(25)16-9(24)3-8(23)4-13(16)31-12/h1-4,12,15,18-24,26-30H,5-6H2/t12-,15+,18+,19-,20+,21+/m0/s1
InChIKey	SNFFBROYEDWRGB-NHXQFOETSA-N
Smiles	C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O
Isomeric SMILES	C1[C@H](OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C(=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O
PubChem CID	174157
Molecular Weight	466.39

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

DMSO(mg / mL) Max Solubility	100
DMSO(mM) Max Solubility	214.412830463775
Water(mg / mL) Max Solubility	-1
Molecular Weight	466.400 g/mol
XLogP3	-0.100
Hydrogen Bond Donor Count	8
Hydrogen Bond Acceptor Count	12
Rotatable Bond Count	4
Exact Mass	466.111 Da
Monoisotopic Mass	466.111 Da
Topological Polar Surface Area	207.000 Å²
Heavy Atom Count	33
Formal Charge	0
Complexity	692.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	6
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Yu Zeng, Jiale Song, Jinfu Li, Chi Yuan. (2023) Influence of Isocyanate Structure on Recyclable Shape Memory Poly(thiourethane). Materials, 16 (11): (4040).

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