gelsemine
group of stereoisomers
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gelsemine
Summary
gelsemine is a group of stereoisomers[1].
Key Facts
- gelsemine's instance of is recorded as group of stereoisomers[2].
- gelsemine's canonical SMILES is recorded as C=CC12CN(C)C3C4COC(CC41)C1(C(=O)Nc4ccccc41)C32[3].
- gelsemine's InChI is recorded as InChI=1S/C20H22N2O2/c1-3-19-10-22(2)16-11-9-24-15(8-13(11)19)20(17(16)19)12-6-4-5-7-14(12)21-18(20)23/h3-7,11,13,15-17H,1,8-10H2,2H3,(H,21,23)[4].
- gelsemine's InChIKey is recorded as NFYYATWFXNPTRM-UHFFFAOYSA-N[5].
- gelsemine's chemical formula is recorded as C₂₀H₂₂N₂O₂[6].
- gelsemine's subclass of is recorded as gelsemine-type alkaloid[7].
- gelsemine's PubChem CID is recorded as 279057[8].
- gelsemine's ChEBI ID is recorded as 181110[9].
- gelsemine's found in taxon is recorded as Gelsemium sempervirens[10].
- gelsemine's found in taxon is recorded as Gelsemium elegans[11].
- gelsemine's Human Metabolome Database ID is recorded as HMDB0252666[12].
- gelsemine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+322.168127944'}[13].
- gelsemine's SureChEMBL ID is recorded as 4279911[14].
- gelsemine's DSSTox substance ID is recorded as DTXSID40871716[15].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR308861[16].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR310576[17].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR304594[18].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR304598[19].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR304602[20].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR304606[21].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR304610[22].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR304614[23].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR304617[24].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR304620[25].
- gelsemine's MassBank accession ID is recorded as MSBNK-RIKEN-PR304624[26].