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Enocyanin , CAS No.11029-12-2

1 Citations

COA

Cas Number: 11029-12-2
EC Number: {"Markup":{"URL":"https://pubchem.ncbi.nlm.nih.gov/compound/cyanidin","Type":"PubChemInternalLink","Extra":"CID-128861","Start":11,"Length":8},{"URL":"https://pubchem.ncbi.nlm.nih.gov/compound/peonidin","Type":"PubChemInternalLink","Extra":"CID-441773","S
PubChem CID: 145858

In stock

Item Number

E648339

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SKU	Size	Availability	Price	Qty
E648339-100mg	100mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$60.90

Flavonoids Anthocyans

View related series

Flavonoids Anthocyans (1) Glucose Metabolism (1943) Metabolic Enzyme/Protease (4860) Phosphatase (222)

Basic Description

Synonyms	Flavylium \| Q-200643 \| Anthocyanidins \| CHEBI:36121 \| 2-phenylchromenylium \| Q27116709 \| 2-phenyl-1$l^{4}-chromen-1-ylium \| InChI=1/C15H11O/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)16-15/h1-11H/q+ \| UNII-F02KPB2508 \| Enocyanin \| F02KPB2508 \| Oenocyanin \|
Biochemical and Physiological Mechanisms	Enocyanin is an anthocyanin extracted from grapes. Enocyanin shows inhibitory effect on the leucine aminopeptidase , acid phosphatase , γ-glutamyl transpeptidase and esterase activity.
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Enocyanin is an anthocyanin extracted from grapes. Enocyanin shows inhibitory effect on the leucine aminopeptidase , acid phosphatase , γ-glutamyl transpeptidase and esterase activity In Vitro Enocyanin (0.1%) affects the leucine aminopeptidase, acid phosphatase, γ-glutamyl transpeptidase and esterase activity by 63%, 100%, 134% and 99%, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:Acid phosphatase

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Phenylpropanoids and polyketides
  - Class Flavonoids
    - Subclass Anthocyanidins

Kingdom	Organic compounds
Superclass	Phenylpropanoids and polyketides
Class	Flavonoids
Subclass	Anthocyanidins
Intermediate Tree Nodes	Not available
Direct Parent	Anthocyanidins
Alternative Parents	1-benzopyrans Benzene and substituted derivatives Heteroaromatic compounds Oxacyclic compounds Organooxygen compounds Hydrocarbon derivatives Organic cations
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Anthocyanidin - 1-benzopyran - Benzopyran - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Oxacycle - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organic cation - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as anthocyanidins. These are sugar-free counterparts of anthocyanins based on the flavylium ion or 2-phenylchromenylium ion.
External Descriptors	chromenyliums
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

Names and Identifiers

IUPAC Name	2-phenylchromenylium
INCHI	InChI=1S/C15H11O/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)16-15/h1-11H/q+1
InChIKey	NWKFECICNXDNOQ-UHFFFAOYSA-N
Smiles	C1=CC=C(C=C1)C2=[O+]C3=CC=CC=C3C=C2
Isomeric SMILES	C1=CC=C(C=C1)C2=[O+]C3=CC=CC=C3C=C2
Alternate CAS	11029-12-2,14051-53-7
PubChem CID	145858
MeSH Entry Terms	Anthocyanidin;Anthocyanidins;Anthocyanin;Anthocyanins;Leucoanthocyanidins

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

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

Analytical Chart:

Chemical and Physical Properties

Solubility	DMSO : ≥ 50 mg/mL H2O : 5 mg/mL (Need ultrasonic)
Molecular Weight	207.250 g/mol
XLogP3
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	1
Exact Mass	207.081 Da
Monoisotopic Mass	207.081 Da
Topological Polar Surface Area	1.000 Å²
Heavy Atom Count	16
Formal Charge	1
Complexity	219.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
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

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