KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (38)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00022225 External link 512 (E)-ent-3beta-3,18-Dihydroxy-8(17),13-labdadien-15-oic acid
C00022226 External link 512 Henrilabdane A
/ (-)-Henrilabdane A
C00022227 External link 512 (14S)-14,15-Dihydroxy-8(17),13(16)-labdadien-19-oic acid
C00022249 External link 512 (ent-13S)-15,16-Dihydroxy-8(17)-labden-18-oic acid
C00022407 External link 512 13S-Hydroxy-7,14-labdadien-19-oic acid
C00022417 External link 512 2alpha-Hydroxy-12Z-ozic acid
CHEMBL434755
C00022418 External link 512 2-Oxo-12Z-ozic acid
C00022442 External link 512 7,13(16)-Labdadiene-15,19-dioic acid
C00022457 External link 512 ent-Labda-8(17),13-dien-19-oic acid-15,16-olide
C00022524 External link 512 Viscidic acid A
/ ent-15-Hydroxy-8(17),13E-labdadien-18-oic acid
CHEMBL511193
C00022708 External link 512 Isocupressic acid
/ (+)-Isocupressic acid
/ 15-Hydroxy-8(17),13E-labdadien-15-oic acid
CHEMBL511193
C110793
C00022721 External link 512 Torulosic acid
/ Cupressic acid
/ 13R-Hydroxy-8(17),14-labdadien-19-oic acid
CHEMBL457163
C00022722 External link 512 13-Epicupressic acid
/ (+)-13-Epicupressic acid
CHEMBL457163
C00022768 External link 512 7,13-Labdadien-15,16-olid-19-oic acid
C00022769 External link 512 ent-8(17),13-Labdadien-15,16-olid-18-oic acid
C00022770 External link 512 Pinusolidic acid
CHEMBL90504
CHEMBL465159
C00023275 External link 512 Isocommunic acid
/ Myrceocommunic acid
C00023283 External link 512 Ozic acid
/ (-)-Ozic acid
CHEMBL498097
CHEMBL1488779
CHEMBL1731589
13 / 14 / 8
C00023285 External link 512 Communic acid
CHEMBL498097
CHEMBL1488779
CHEMBL1731589
13 / 14 / 8
C00023287 External link 512 Z-Communic acid
/ Elliotinoic acid
/ (Z)-Communic acid
/ cis-Communic acid
CHEMBL498097
CHEMBL1488779
CHEMBL1731589
13 / 14 / 8
C00023290 External link 512 (13S)-7-Labdene-15,18-dioic acid
C00023291 External link 512 Pinifolic acid
CHEMBL2048915
C00023300 External link 512 Imbricatoloic acid
CHEMBL2048004
C00023301 External link 512 Acetylimbricatolic acid
C00023303 External link 512 Junicedric acid
CHEMBL2048915
C00023304 External link 512 Oliveric acid
CHEMBL2048915
C00023344 External link 512 Nivenolide
CHEMBL90504
CHEMBL465159
C00023425 External link 512 ent-15-Nor-14-oxo-8(17),12E-labdadiene-18-oic acid
CHEMBL497937
C00023428 External link 512 Acrostalic acid
C00023429 External link 512 LL-Z1271beta
CHEMBL1077022
CHEMBL2011788
C00029408 External link 512 16-Hydroxy communic acid
C00031513 External link 512 15-Methoxypinusolidic acid
/ (+)-15-Methoxypinusolidic acid
C00032600 External link 512 14,15,-Bisnor-8(17)-labdene-16,19-dioic acid
C00033908 External link 512 Henrilabdane B
/ (-)-Henrilabdane B
C00033909 External link 512 Henrilabdane C
/ (+)-Henrilabdane C
C00036233 External link 512 trans-Communic acid
CHEMBL498097
CHEMBL1488779
CHEMBL1731589
13 / 14 / 8
C00038087 External link 512 (+)-trans-Ozic acid
CHEMBL498097
CHEMBL1488779
CHEMBL1731589
13 / 14 / 8
C00040738 External link 512 (-)-ent-trans-Communic acid
CHEMBL498097
CHEMBL1488779
CHEMBL1731589
13 / 14 / 8

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 0 / 0
P06746 DNA polymerase beta Enzyme C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 0 / 0
P39748 Flap endonuclease 1 Enzyme C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 7 / 3
Q9Y253 DNA polymerase eta Enzyme C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 4 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00023283 C00023285 C00023287 C00036233 C00038087 C00040738 2 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (14)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#114500 Colorectal cancer; crc Q14191
#600274 Frontotemporal dementia; ftd P10636
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (8)

KEGG name UniProt
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00296 Defects in RecQ helicases Q14191 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)