PCIDB

KNApSAcK Metabolite C00010301

Metabolite

KNApSAcK Entry

id C00010301
Name Coriandrol / (S)-Linalool / S-(+)-Linalool / (+)-S-Linalool / (S)-3,7-Dimethyl-1,6-octadien-3-ol
CAS RN 126-90-9
Standard InChI InChI=1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3/t10-/m1/s1
Standard InChI (Main Layer) InChI=1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3

Cluster

Phytochemical cluster No. 34
KCF-S cluster No. 958

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL25306 CHEMBL235672

KEGG

By LinkDB C11389

CTD

By CAS RN

Human Protein / Gene in interaction

6 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P22310 UDP-glucuronosyltransferase 1-4 Enzyme CHEMBL25306 CHEMBL1908082 (1)
3 / 0
P10828 Thyroid hormone receptor beta NR1A2 CHEMBL25306 CHEMBL1794561 (1)
3 / 1
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL25306 CHEMBL1794401 (1)
0 / 0
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme CHEMBL25306 CHEMBL1908088 (1)
0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme CHEMBL235672 CHEMBL1614240 (1)
0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme CHEMBL25306 CHEMBL1908080 (1)
5 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#143500 Gilbert syndrome P22309
P22310
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828

KEGG DISEASE (2)

KEGG disease name UniProt
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00208 Hyperbilirubinemia P22309 (related)