Lanceolarin , CAS No.15914-68-8

CAS: 15914-68-8 Cat. No.: L961403 PubChem CID: 5492234
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Storage
Room temperature
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Dimensione
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1mg
L961403-1mg
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5mg
L961403-5mg
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10mg
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Specifiche

Condizioni di conservazione di stoccaggio
Room temperature
Tipo di azione
INHIBITOR
Nomi e identificatori
Sorrisi canonici
COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O
IUPAC Name
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-methoxyphenyl)chromen-4-one
InChIKey
VGKGODYADVWBQB-NRIIMPDMSA-N
INCHI
1S/C27H30O14/c1-36-13-4-2-12(3-5-13)15-8-37-17-7-14(6-16(29)19(17)20(15)30)40-25-23(33)22(32)21(31)18(41-25)9-38-26-24(34)27(35,10-28)11-39-26/h2-8,18,21-26,28-29,31-35H,9-11H2,1H3/t18-,21-,22+,23-,24+,25-,26-,27-/m1/s1
Isomeri SMILES
COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO[C@H]5[C@@H]([C@](CO5)(CO)O)O)O)O)O
CAS alternativo
15914-68-8
PubChem CID
5492234
Termini MeSH
biochanin-A-7-apiosyl(1-2)glucoside;lanceolarin

Dati avanzati

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassPhenylpropanoids and polyketides
ClasseIsoflavonoids
SubclassIsoflavonoid O-glycosides
Intermediate Tree Nodes Not available
Direct ParentIsoflavonoid O-glycosides
Alternative Parents 4'-O-methylisoflavones  Hydroxyisoflavonoids  Isoflavones  Phenolic glycosides  Chromones  Disaccharides  O-glycosyl compounds  Phenoxy compounds  Anisoles  Methoxybenzenes  Pyranones and derivatives  Alkyl aryl ethers  1-hydroxy-2-unsubstituted benzenoids  1-hydroxy-4-unsubstituted benzenoids  Oxanes  Oxolanes  Vinylogous acids  Heteroaromatic compounds  Tertiary alcohols  Secondary alcohols  Polyols  Oxacyclic compounds  Acetals  Organic oxides  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Isoflavonoid o-glycoside - Isoflavonoid-7-o-glycoside - 4p-o-methylisoflavone - Isoflavone - Hydroxyisoflavonoid - Phenolic glycoside - O-glycosyl compound - Glycosyl compound - Disaccharide - Chromone - 1-benzopyran - Benzopyran - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Pyran - Monocyclic benzene moiety - Oxane - Benzenoid - Heteroaromatic compound - Oxolane - Tertiary alcohol - Vinylogous acid - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Ether - Organic oxygen compound - Alcohol - Primary alcohol - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.
External Descriptors Isoflavonoids
Struttura 3D
Modello di struttura chimica interattiva





Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
Peso molecolare578.500 g/mol
XLogP3-0.600
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count14
Rotatable Bond Count8
Exact Mass578.164 Da
Monoisotopic Mass578.164 Da
Topological Polar Surface Area214.000 Ų
Heavy Atom Count41
Formal Charge0
Complexity939.000
Isotope Atom Count0
Defined Atom Stereocenter Count8
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

Domande frequenti

How should this product be stored?
Store at room temperature.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 15914-68-8. InChIKey VGKGODYADVWBQB-NRIIMPDMSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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