Metabolite

KNApSAcK Entry

id C00003197
Name Valerenic acid
CAS RN 3569-10-6
Standard InChI InChI=1S/C15H22O2/c1-9-4-6-12(8-11(3)15(16)17)14-10(2)5-7-13(9)14/h8-9,12-13H,4-7H2,1-3H3,(H,16,17)/b11-8-/t9-,12+,13-/m1/s1
Standard InChI (Main Layer) InChI=1S/C15H22O2/c1-9-4-6-12(8-11(3)15(16)17)14-10(2)5-7-13(9)14/h8-9,12-13H,4-7H2,1-3H3,(H,16,17)

Cluster

Phytochemical cluster No. 38
KCF-S cluster No. 2317

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL1545045

KEGG

By LinkDB C09743

CTD

By CAS RN C037133

Species

Summary

Plant class

class name count
asterids 1

Family

family name count
Caprifoliaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Valeriana officinalis 19953 Caprifoliaceae asterids Viridiplantae

Human Protein / Gene in interaction

8 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 CHEMBL1545045 CHEMBL1794524 (1) CHEMBL1794552 (1)
0 / 0
P16473 Thyrotropin receptor Glycohormone receptor CHEMBL1545045 CHEMBL1614281 (1) CHEMBL1614361 (1)
3 / 2
P19793 Retinoic acid receptor RXR-alpha NR2B1 CHEMBL1545045 CHEMBL1794371 (1)
0 / 0
P00352 Retinal dehydrogenase 1 Enzyme CHEMBL1545045 CHEMBL1614458 (1)
0 / 0
P10145 Interleukin-8 Secreted protein CHEMBL1545045 CHEMBL2114835 (1)
0 / 0
P04150 Glucocorticoid receptor NR3C1 CHEMBL1545045 CHEMBL1794456 (1)
0 / 1
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 CHEMBL1545045 CHEMBL2114842 (1)
0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein CHEMBL1545045 CHEMBL2114890 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (3)

OMIM preferred title UniProt
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473

KEGG DISEASE (3)

KEGG disease name UniProt
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)