(RS)-eflornithine
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(RS)-eflornithine
Summary
(RS)-eflornithine is a group of stereoisomers[1]. (RS)-eflornithine draws 105 Wikipedia views per month (group_of_stereoisomers category, ranking #143 of 1,063).[2]
Key Facts
- (RS)-eflornithine's instance of is recorded as group of stereoisomers[3].
- (RS)-eflornithine's chemical structure is recorded as (±)-Eflornithin Structural Formulae V.1.svg[4].
- (RS)-eflornithine's chemical structure is recorded as Eflornithine.svg[5].
- (RS)-eflornithine's physically interacts with is recorded as Ornithine decarboxylase 1[6].
- (RS)-eflornithine's CAS Registry Number is recorded as 70052-12-9[7].
- (RS)-eflornithine's canonical SMILES is recorded as C(CC(C(F)F)(C(=O)O)N)CN[8].
- (RS)-eflornithine's InChI is recorded as InChI=1S/C6H12F2N2O2/c7-4(8)6(10,5(11)12)2-1-3-9/h4H,1-3,9-10H2,(H,11,12)[9].
- (RS)-eflornithine's InChIKey is recorded as VLCYCQAOQCDTCN-UHFFFAOYSA-N[10].
- (RS)-eflornithine's ATC code is recorded as P01CX03[11].
- (RS)-eflornithine's ATC code is recorded as D11AX16[12].
- (RS)-eflornithine's chemical formula is recorded as C₆H₁₂F₂N₂O₂[13].
- (RS)-eflornithine's subclass of is recorded as bactericide[14].
- (RS)-eflornithine's Commons category is recorded as Eflornithine[15].
- (RS)-eflornithine's MeSH descriptor ID is recorded as D000518[16].
- (RS)-eflornithine's ChEMBL ID is recorded as CHEMBL830[17].
- (RS)-eflornithine's Guide to Pharmacology Ligand ID is recorded as 5176[18].
- (RS)-eflornithine's Freebase ID is recorded as /m/052ssm[19].
- (RS)-eflornithine's UNII is recorded as ZQN1G5V6SR[20].
- (RS)-eflornithine's ChemSpider ID is recorded as 2902[21].
- (RS)-eflornithine's PubChem CID is recorded as 3009[22].
- (RS)-eflornithine's KEGG ID is recorded as D07883[23].
- (RS)-eflornithine's MeSH tree code is recorded as D12.125.068.665.340[24].
- (RS)-eflornithine's MeSH tree code is recorded as D12.125.095.765.340[25].
- (RS)-eflornithine's ChEBI ID is recorded as 41948[26].
- (RS)-eflornithine's DrugBank ID is recorded as DB06243[27].
Why It Matters
(RS)-eflornithine draws 105 Wikipedia views per month (group_of_stereoisomers category, ranking #143 of 1,063).[2] (RS)-eflornithine has Wikipedia articles in 17 language editions, a strong signal of global cultural recognition.[28] (RS)-eflornithine is known by 16 alternative names across languages and contexts.[29]