carveol
chemical compound
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carveol
Summary
carveol is a group of stereoisomers[1]. carveol draws 19 Wikipedia views per month (group_of_stereoisomers category, ranking #207 of 1,063).[2]
Key Facts
- carveol's instance of is recorded as group of stereoisomers[3].
- carveol's chemical structure is recorded as Carveol non-stereo.png[4].
- carveol's physically interacts with is recorded as Transient receptor potential cation channel, subfamily V, member 3[5].
- carveol's CAS Registry Number is recorded as 99-48-9[6].
- carveol's EC number is recorded as 202-757-4[7].
- carveol's canonical SMILES is recorded as CC1=CCC(CC1O)C(=C)C[8].
- carveol's InChI is recorded as InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3[9].
- carveol's InChIKey is recorded as BAVONGHXFVOKBV-UHFFFAOYSA-N[10].
- carveol's chemical formula is recorded as C₁₀H₁₆O[11].
- carveol's subclass of is recorded as menthane monoterpenoids[12].
- carveol's Commons category is recorded as Carveol[13].
- carveol's ChEMBL ID is recorded as CHEMBL1385229[14].
- carveol's Guide to Pharmacology Ligand ID is recorded as 6417[15].
- carveol's Freebase ID is recorded as /m/0bk095[16].
- carveol's RTECS number is recorded as OS8400000[17].
- carveol's ChemSpider ID is recorded as 7160[18].
- carveol's PubChem CID is recorded as 7438[19].
- carveol's KEGG ID is recorded as C11395[20].
- carveol's ChEBI ID is recorded as 23046[21].
- carveol's found in taxon is recorded as Lavandula latifolia[22].
- carveol's found in taxon is recorded as Citrus ×iyo[23].
- carveol's found in taxon is recorded as Achillea erba-rotta[24].
- carveol's found in taxon is recorded as Achillea moschata[25].
- carveol's found in taxon is recorded as Achillea nana[26].
- carveol's found in taxon is recorded as Achillea nobilis[27].
Why It Matters
carveol draws 19 Wikipedia views per month (group_of_stereoisomers category, ranking #207 of 1,063).[2] carveol has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] carveol is known by 3 alternative names across languages and contexts.[29]