Metabolite

KNApSAcK Entry

id C00045634
Name Anchoic acid
CAS RN 123-99-9
Standard InChI InChI=1S/C9H16O4/c10-8(11)6-4-2-1-3-5-7-9(12)13/h1-7H2,(H,10,11)(H,12,13)
Standard InChI (Main Layer) InChI=1S/C9H16O4/c10-8(11)6-4-2-1-3-5-7-9(12)13/h1-7H2,(H,10,11)(H,12,13)

Cluster

Phytochemical cluster
KCF-S cluster No. 1853

Link

ChEMBL

By standard InChI CHEMBL1238
By standard InChI Main Layer CHEMBL1238

KEGG

By LinkDB C08261

CTD

By CAS RN C010038

Species

Summary

Plant class

class name count
asterids 1

Family

family name count
Lamiaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Schnabelia tetradonta 167918 Lamiaceae asterids Viridiplantae

Human Protein / Gene in interaction

17 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 CHEMBL1238 CHEMBL1741321 (1)
1 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein CHEMBL1238 CHEMBL1738312 (1)
0 / 0
Q99895 Chymotrypsin-C S1A CHEMBL1238 CHEMBL660318 (1)
0 / 2
P02545 Prelamin-A/C Unclassified protein CHEMBL1238 CHEMBL1614544 (2)
11 / 10
P16473 Thyrotropin receptor Glycohormone receptor CHEMBL1238 CHEMBL1614281 (1) CHEMBL1614361 (1)
3 / 2
P40925 Malate dehydrogenase, cytoplasmic Enzyme CHEMBL1238 CHEMBL709633 (1)
0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 CHEMBL1238 CHEMBL1741325 (1)
0 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein CHEMBL1238 CHEMBL1614166 (1) CHEMBL1738096 (1)
CHEMBL1738622 (1)
1 / 0
O75496 Geminin Unclassified protein CHEMBL1238 CHEMBL2114780 (1)
0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 CHEMBL1238 CHEMBL1741322 (1)
0 / 0
Q01453 Peripheral myelin protein 22 Unclassified protein CHEMBL1238 CHEMBL1614171 (1)
5 / 2
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor CHEMBL1238 CHEMBL1614274 (1) CHEMBL1613823 (1)
0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 CHEMBL1238 CHEMBL1741323 (1)
1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 CHEMBL1238 CHEMBL1741324 (1)
0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme CHEMBL1238 CHEMBL1614211 (1)
0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme CHEMBL1238 CHEMBL1738442 (1)
0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein CHEMBL1238 CHEMBL2354287 (1)
1 / 1

CTD interaction (8)

compound gene gene name gene description interaction interaction type form reference
pmid
C010038 5327 PLAT
T-PA
TPA
plasminogen activator, tissue (EC:3.4.21.68) azelaic acid results in decreased expression of and results in decreased secretion of PLAT protein decreases expression
/ decreases secretion
protein 8635147
C010038 5327 PLAT
T-PA
TPA
plasminogen activator, tissue (EC:3.4.21.68) azelaic acid results in decreased expression of PLAT mRNA decreases expression
mRNA 8635147
C010038 5328 PLAU
ATF
BDPLT5
QPD
UPA
URK
u-PA
plasminogen activator, urokinase (EC:3.4.21.73) azelaic acid results in decreased expression of and results in decreased secretion of PLAU protein decreases expression
/ decreases secretion
protein 8635147
C010038 5328 PLAU
ATF
BDPLT5
QPD
UPA
URK
u-PA
plasminogen activator, urokinase (EC:3.4.21.73) azelaic acid results in decreased expression of PLAU mRNA decreases expression
mRNA 8635147
C010038 5468 PPARG
CIMT1
GLM1
NR1C3
PPARG1
PPARG2
PPARgamma
peroxisome proliferator-activated receptor gamma azelaic acid results in increased activity of PPARG protein increases activity
protein 20545756
C010038 5468 PPARG
CIMT1
GLM1
NR1C3
PPARG1
PPARG2
PPARgamma
peroxisome proliferator-activated receptor gamma azelaic acid results in increased expression of PPARG mRNA increases expression
mRNA 20545756
C010038 5054 SERPINE1
PAI
PAI-1
PAI1
PLANH1
serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 azelaic acid results in increased expression of and results in increased secretion of SERPINE1 protein increases expression
/ increases secretion
protein 8635147
C010038 5054 SERPINE1
PAI
PAI-1
PAI1
PLANH1
serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 azelaic acid results in increased expression of SERPINE1 mRNA increases expression
mRNA 8635147

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (23)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#118300 Charcot-marie-tooth disease and deafness Q01453
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#139393 Guillain-barre syndrome, familial; gbs Q01453
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#145900 Hypertrophic neuropathy of dejerine-sottas Q01453
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#275210 Restrictive dermopathy, lethal P02545

KEGG DISEASE (19)

KEGG disease name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
Q01453 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00932 Tropical calcific pancreatitis Q99895 (related)
H00933 Hereditary pancreatitis Q99895 (related)

Diseases related to CTD interactions

11 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D000152 C010038 Acne Vulgaris therapeutic
17456913
18246693
20394495
20482689
20545756
21612319
21637899
22111946
D050197 C010038 Atherosclerosis therapeutic
19880116
D003876 C010038 Dermatitis, Atopic therapeutic
19804495
D019557 C010038 Dermatitis, Perioral therapeutic
19804495
D018327 C010038 Hutchinson's Melanotic Freckle therapeutic
8635147
D017495 C010038 Hyperpigmentation therapeutic
20804622
21637899
D007249 C010038 Inflammation therapeutic
18803456
20545756
D008548 C010038 Melanosis therapeutic
22151936
D011565 C010038 Psoriasis therapeutic
20684146
D012393 C010038 Rosacea therapeutic
17472690
17500380
18561584
18803456
19363903
19588640
20545756
20645521
20967185
21916272
22111946
D012871 C010038 Skin Diseases therapeutic
20025951