Resorcinol

Representations & DB's id
ChEBI:	CHEBI:27810
ChEMBL:	CHEMBL24147
PubChem:	5054
IUPAC:	benzene-1,3-diol
Standard InChI:	InChI=1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H
Standard InChI Key:	GHMLBKRAJCXXBS-UHFFFAOYSA-N
SMILES:	Oc1cccc(c1)O

Molecular propeties
AlogP:	1.1
Hydrogen bonds acceptors:	2
Hydrogen bonds donors:	2
Rotatable bonds:	0
Number of rings:	1
Molecular Weight:	110.04
Topological polar surface area:	40.5
Number of aromatic rings:	1
Fsp3:	0
Number of carbons:	6

Plant sources

Part of plant	Plant name	Ref.
Fructus	Foeniculum vulgare

Activity Type	Activity Value	Target Name	UniProt ID
Ki	795000 nM	Carbonic anhydrase I	P00915
Ki	7700 nM	Carbonic anhydrase II	P00918
Ki	10700 nM	Carbonic anhydrase XIV	Q9ULX7
Ki	7500 nM	Carbonic anhydrase XII	O43570
Ki	69700 nM	Carbonic anhydrase IX	Q16790
Ki	644000 nM	Carbonic anhydrase VII	P43166
Ki	550000 nM	Carbonic anhydrase VI	P23280
Ki	7100 nM	Carbonic anhydrase VB	Q9Y2D0
Ki	8700 nM	Carbonic anhydrase VA	P35218
Ki	570000 nM	Carbonic anhydrase IV	P22748
Ki	605000 nM	Carbonic anhydrase III	P07451
Ki	7700 nM	Carbonic anhydrase II	P00918
Ki	795000 nM	Carbonic anhydrase I	P00915
Potency	1000 nM	Prelamin-A/C	P02545
Potency	44668.4 nM	Aldehyde dehydrogenase 1A1	P00352
Potency	31622.8 nM	Endoplasmic reticulum-associated amyloid beta-peptide-binding protein	Q99714
Potency	10000 nM	Cytochrome P450 3A4	P08684
Potency	10000 nM	Cytochrome P450 3A4	P08684
Potency	66824.2 nM	Nuclear factor erythroid 2-related factor 2	Q16236
Potency	13335.9 nM	Geminin	O75496
Potency	74978 nM	Interleukin-8	P10145
Potency	74978 nM	Nuclear receptor ROR-gamma	P51449
Others	75 %	Tyrosinase	P14679
Others	37 %	Tyrosinase	P14679
Others	26 %	Tyrosinase	P14679
Others	32 %	Tyrosinase	P14679
Others	91.8 %	Cytochrome P450 19A1	P11511
Ki	795000 nM	Carbonic anhydrase I	P00915
Ki	7700 nM	Carbonic anhydrase II	P00918