(±)-goitrin
group of stereoisomers
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(±)-goitrin
Summary
(±)-goitrin is a group of stereoisomers[1]. (±)-goitrin draws 9 Wikipedia views per month (group_of_stereoisomers category, ranking #211 of 1,063).[2]
Key Facts
- (±)-goitrin's instance of is recorded as group of stereoisomers[3].
- (±)-goitrin's chemical structure is recorded as Goitrin.png[4].
- (±)-goitrin's CAS Registry Number is recorded as 13190-34-6[5].
- (±)-goitrin's EC number is recorded as 236-145-3[6].
- (±)-goitrin's canonical SMILES is recorded as C=CC1CNC(=S)O1[7].
- (±)-goitrin's InChI is recorded as InChI=1S/C5H7NOS/c1-2-4-3-6-5(8)7-4/h2,4H,1,3H2,(H,6,8)[8].
- (±)-goitrin's InChIKey is recorded as UZQVYLOFLQICCT-UHFFFAOYSA-N[9].
- (±)-goitrin's chemical formula is recorded as C₅H₇NOS[10].
- (±)-goitrin's subclass of is recorded as oxazolidine alkaloid[11].
- (±)-goitrin's ChEMBL ID is recorded as CHEMBL508652[12].
- (±)-goitrin's Freebase ID is recorded as /m/05mrgpp[13].
- (±)-goitrin's UNII is recorded as O8KVD7J2P5[14].
- (±)-goitrin's ChemSpider ID is recorded as 2299106[15].
- (±)-goitrin's PubChem CID is recorded as 3034683[16].
- (±)-goitrin's ChEBI ID is recorded as 183227[17].
- (±)-goitrin's found in taxon is recorded as Isatis tinctoria[18].
- (±)-goitrin's has characteristic is recorded as bitterness[19].
- (±)-goitrin's Human Metabolome Database ID is recorded as HMDB0251849[20].
- (±)-goitrin's mass is recorded as {'unit': 'Q483261', 'amount': '+129.025'}[21].
- (±)-goitrin's Nikkaji ID is recorded as J21.392F[22].
- (±)-goitrin's ECHA Substance Infocard ID is recorded as 100.032.845[23].
- (±)-goitrin's SureChEMBL ID is recorded as 340219[24].
- (±)-goitrin's DSSTox substance ID is recorded as DTXSID10274235[25].
- (±)-goitrin's Microsoft Academic ID is recorded as 2779478331[26].
- (±)-goitrin's MassBank accession ID is recorded as MSBNK-NaToxAq-NA002576[27].
Why It Matters
(±)-goitrin draws 9 Wikipedia views per month (group_of_stereoisomers category, ranking #211 of 1,063).[2] (±)-goitrin has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] (±)-goitrin is known by 3 alternative names across languages and contexts.[29]