trans-astringin
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trans-astringin
Summary
trans-astringin is a type of chemical entity[1]. trans-astringin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (2 views/month).[2]
Key Facts
- trans-astringin's instance of is recorded as type of chemical entity[3].
- trans-astringin's CAS Registry Number is recorded as 29884-49-9[4].
- trans-astringin's canonical SMILES is recorded as C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O[5].
- trans-astringin's InChI is recorded as InChI=1S/C20H22O9/c21-9-16-17(25)18(26)19(27)20(29-16)28-13-6-11(5-12(22)8-13)2-1-10-3-4-14(23)15(24)7-10/h1-8,16-27H,9H2/b2-1+/t16-,17-,18+,19-,20-/m1/s1[6].
- trans-astringin's InChIKey is recorded as PERPNFLGJXUDDW-CUYWLFDKSA-N[7].
- trans-astringin's chemical formula is recorded as C₂₀H₂₂O₉[8].
- trans-astringin's subclass of is recorded as stilbenoid[9].
- trans-astringin's subclass of is recorded as aromatic polyketide[10].
- trans-astringin's has part is recorded as carbon[11].
- trans-astringin's ChEMBL ID is recorded as CHEMBL358769[12].
- trans-astringin's Freebase ID is recorded as /m/0gjb0vk[13].
- trans-astringin's UNII is recorded as 4ER6YKM4YL[14].
- trans-astringin's ChemSpider ID is recorded as 4445028[15].
- trans-astringin's PubChem CID is recorded as 5281712[16].
- trans-astringin's KEGG ID is recorded as C10245[17].
- trans-astringin's ChEBI ID is recorded as 2899[18].
- trans-astringin's found in taxon is recorded as Picea abies[19].
- trans-astringin's found in taxon is recorded as Picea sitchensis[20].
- trans-astringin's found in taxon is recorded as Guibourtia coleosperma[21].
- trans-astringin's found in taxon is recorded as Abies nephrolepis[22].
- trans-astringin's found in taxon is recorded as Fagopyrum megacarpum[23].
- trans-astringin's found in taxon is recorded as Fallopia japonica var. japonica[24].
- trans-astringin's found in taxon is recorded as Vitis vinifera[25].
- trans-astringin's Reaxys registry number is recorded as 1408080[26].
- trans-astringin's isomeric SMILES is recorded as C1=CC(=C(C=C1/C=C/C2=CC(=CC(=C2)O[C@H]3C@@HO)O)O)OC@@HO)O)O)O">[27].
Why It Matters
trans-astringin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (2 views/month).[2] trans-astringin has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] trans-astringin is known by 5 alternative names across languages and contexts.[29]