Vescalagin
group of stereoisomers
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Vescalagin
Summary
Vescalagin is a group of stereoisomers[1].
Key Facts
- Vescalagin's instance of is recorded as group of stereoisomers[2].
- Vescalagin's physically interacts with is recorded as taste receptor type 2[3].
- Vescalagin's CAS Registry Number is recorded as 24312-00-3[4].
- Vescalagin's canonical SMILES is recorded as O=C1OCC2OC(=O)C3=CC(O)=C(O)C(O)=C3C4=C(O)C(O)=C(O)C5=C4C(=O)OC(C6OC(=O)C7=C5C(O)=C(O)C(O)=C7C6O)C2OC(=O)C8=CC(O)=C(O)C(O)=C8C9=C(O)C(O)=C(O)C=C19[5].
- Vescalagin's InChI is recorded as InChI=1S/C41H26O26/c42-8-1-5-12(24(48)21(8)45)13-6(2-9(43)22(46)25(13)49)39(60)65-34-11(4-63-37(5)58)64-38(59)7-3-10(44)23(47)26(50)14(7)15-18-16(28(52)32(56)27(15)51)17-19-20(30(54)33(57)29(17)53)31(55)35(66-41(19)62)36(34)67-40(18)61/h1-3,11,31,34-36,42-57H,4H2[6].
- Vescalagin's InChIKey is recorded as UDYKDZHZAKSYCO-UHFFFAOYSA-N[7].
- Vescalagin's chemical formula is recorded as C₄₁H₂₆O₂₆[8].
- Vescalagin's subclass of is recorded as chemical compound[9].
- Vescalagin's PubChem CID is recorded as 168165[10].
- Vescalagin's found in taxon is recorded as pomegranate[11].
- Vescalagin's found in taxon is recorded as Castanea mollissima[12].
- Vescalagin's found in taxon is recorded as Q156137[13].
- Vescalagin's found in taxon is recorded as Quercus faginea[14].
- Vescalagin's Human Metabolome Database ID is recorded as HMDB0030602[15].
- Vescalagin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+934.0712309520007'}[16].
- Vescalagin's SureChEMBL ID is recorded as 12477174[17].
- Vescalagin's SureChEMBL ID is recorded as 29370035[18].
- Vescalagin's DSSTox substance ID is recorded as DTXSID201029283[19].
- Vescalagin's UniChem compound ID is recorded as 420001[20].