Lanceolarin , CAS No.15914-68-8

CAS: 15914-68-8 Cat. No.: L961403 PubChem CID: 5492234
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Spezifikationen

Storage
Room temperature
Aktionsart
INHIBITOR
Namen und Kennungen
Kanonisches Lächeln
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
Isomere 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
Alternative CAS-Nummer
15914-68-8
PubChem CID
5492234
MeSH-Eintrag
biochanin-A-7-apiosyl(1-2)glucoside;lanceolarin

Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassPhenylpropanoids and polyketides
KlasseIsoflavonoids
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
BeschreibungThis 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
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemische und physikalische Eigenschaften
Molekulargewicht578.500 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
Lösungsrechner
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Häufig gestellte Fragen

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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