(RS)-AMPA
pair of enantiomers
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(RS)-AMPA
Summary
(RS)-AMPA is a group of stereoisomers[1]. (RS)-AMPA draws 48 Wikipedia views per month (group_of_stereoisomers category, ranking #180 of 1,063).[2]
Key Facts
- (RS)-AMPA's instance of is recorded as group of stereoisomers[3].
- (RS)-AMPA's chemical structure is recorded as AMPA.svg[4].
- (RS)-AMPA's CAS Registry Number is recorded as 77521-29-0[5].
- (RS)-AMPA's canonical SMILES is recorded as CC1=C(C(=O)NO1)CC(C(=O)O)N[6].
- (RS)-AMPA's InChI is recorded as InChI=1S/C7H10N2O4/c1-3-4(6(10)9-13-3)2-5(8)7(11)12/h5H,2,8H2,1H3,(H,9,10)(H,11,12)[7].
- (RS)-AMPA's InChIKey is recorded as UUDAMDVQRQNNHZ-UHFFFAOYSA-N[8].
- (RS)-AMPA's chemical formula is recorded as C₇H₁₀N₂O₄[9].
- (RS)-AMPA's subclass of is recorded as non-proteinogenic amino acid[10].
- (RS)-AMPA's subclass of is recorded as isoxazole[11].
- (RS)-AMPA's Commons category is recorded as AMPA[12].
- (RS)-AMPA's ChEMBL ID is recorded as CHEMBL13378[13].
- (RS)-AMPA's Guide to Pharmacology Ligand ID is recorded as 4131[14].
- (RS)-AMPA's Guide to Pharmacology Ligand ID is recorded as 4077[15].
- (RS)-AMPA's Freebase ID is recorded as /m/020v5k[16].
- (RS)-AMPA's UNII is recorded as J090588E6X[17].
- (RS)-AMPA's ChemSpider ID is recorded as 1184[18].
- (RS)-AMPA's PubChem CID is recorded as 1221[19].
- (RS)-AMPA's PubChem CID is recorded as 44373828[20].
- (RS)-AMPA's ChEBI ID is recorded as 34018[21].
- (RS)-AMPA's different from is recorded as AMPA[22].
- (RS)-AMPA's Human Metabolome Database ID is recorded as HMDB0248356[23].
- (RS)-AMPA's mass is recorded as {'unit': 'Q483261', 'amount': '+186.064057'}[24].
- (RS)-AMPA's SureChEMBL ID is recorded as 68799[25].
- (RS)-AMPA's SureChEMBL ID is recorded as 6687427[26].
- (RS)-AMPA's DSSTox substance ID is recorded as DTXSID20868301[27].
Why It Matters
(RS)-AMPA draws 48 Wikipedia views per month (group_of_stereoisomers category, ranking #180 of 1,063).[2] (RS)-AMPA has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[28]