KCF-S cluster No. 3537 (3 metabolites)

Corresponding Phytochemical cluster No. 54


Plant Species


Cumulative plant class count

class name count
rosids 2
Spermatophyta 1

Cumulative family count

class name count
Meliaceae 2
Pinaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Androstane 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Androstane C00280 C00003644

Metabolite list (3)

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
C00003644 External link 512 Androstenedione
CHEMBL274826
CHEMBL1596627
CHEMBL2140059
CHEMBL2311155
D000735
35 / 46 / 31 19 / 2
C00046996 External link 512 6alpha-Hydroxyandrosta-1,4-diene-3,17-dione
C00047005 External link 512 Androsta-1,4-diene-3,17-dione
/ (+)-Androsta-1,4-diene-3,17-dione
CHEMBL1078534
CHEMBL1554587
C006573
5 / 2 / 3

Human Protein / Gene in interactions

38 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00003644 C00047005 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00003644 C00047005 2 / 2
Q16637 Survival motor neuron protein Unclassified protein C00003644 4 / 1
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00003644 2 / 2
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00003644 0 / 0
O15245 Solute carrier family 22 member 1 Drug uniporter C00003644 0 / 0
P02545 Prelamin-A/C Unclassified protein C00003644 11 / 10
P16473 Thyrotropin receptor Glycohormone receptor C00003644 3 / 2
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00003644 0 / 0
P31213 3-oxo-5-alpha-steroid 4-dehydrogenase 2 Oxidoreductase C00003644 1 / 1
P54132 Bloom syndrome protein Enzyme C00003644 1 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00003644 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00003644 0 / 0
P04278 Sex hormone-binding globulin Secreted protein C00003644 0 / 0
P42330 Aldo-keto reductase family 1 member C3 Enzyme C00003644 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00003644 2 / 0
O75496 Geminin Unclassified protein C00003644 0 / 0
P18405 3-oxo-5-alpha-steroid 4-dehydrogenase 1 Oxidoreductase C00003644 0 / 0
P10145 Interleukin-8 Secreted protein C00003644 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003644 2 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00047005 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00003644 0 / 1
Q99700 Ataxin-2 Unclassified protein C00003644 1 / 1
P37058 Testosterone 17-beta-dehydrogenase 3 Enzyme C00003644 1 / 1
P28482 Mitogen-activated protein kinase 1 Erk C00003644 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00003644 3 / 3
Q01453 Peripheral myelin protein 22 Unclassified protein C00003644 5 / 2
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00003644 0 / 0
P03372 Estrogen receptor NR3A1 C00003644 1 / 1
P08185 Corticosteroid-binding globulin Secreted protein C00003644 1 / 1
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00003644 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00047005 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00003644 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00003644 1 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00003644 0 / 0
P10275 Androgen receptor NR3C4 C00003644 3 / 4
P56937 3-keto-steroid reductase Enzyme C00047005 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00003644 1 / 1

19 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
64240 ABCG5, STSL ATP-binding cassette, sub-family G (WHITE), member 5 C00003644
64241 ABCG8, GBD4, STSL ATP-binding cassette, sub-family G (WHITE), member 8 C00003644
8644 AKR1C3, DD3, DDX, HA1753, HAKRB, HAKRe, HSD17B5, PGFS, hluPGFS aldo-keto reductase family 1, member C3 (EC:1.3.1.20 1.1.1.188 1.1.1.239 1.1.1.64 1.1.1.112 1.1.1.357) C00003644
367 AR, AIS, DHTR, HUMARA, HYSP1, KD, NR3C4, SBMA, SMAX1, TFM androgen receptor C00003644
1387 CREBBP, CBP, KAT3A, RSTS CREB binding protein (EC:2.3.1.48) C00003644
1586 CYP17A1, CPT7, CYP17, P450C17, S17AH cytochrome P450, family 17, subfamily A, polypeptide 1 (EC:1.14.99.9 4.1.2.30) C00003644
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) C00003644
2938 GSTA1, GST2, GSTA1-1, GTH1 glutathione S-transferase alpha 1 (EC:2.5.1.18) C00003644
2939 GSTA2, GST2, GSTA2-2, GTA2, GTH2 glutathione S-transferase alpha 2 (EC:2.5.1.18) C00003644
2940 GSTA3, GSTA3-3, GTA3 glutathione S-transferase alpha 3 (EC:2.5.1.18) C00003644
3294 HSD17B2, EDH17B2, HSD17, SDR9C2 hydroxysteroid (17-beta) dehydrogenase 2 (EC:1.1.1.62 1.1.1.239) C00003644
3293 HSD17B3, EDH17B3, SDR12C2 hydroxysteroid (17-beta) dehydrogenase 3 (EC:1.1.1.64) C00003644
3283 HSD3B1, 3BETAHSD, HSD3B, HSDB3, HSDB3A, I, SDR11E1 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 (EC:1.1.1.145 5.3.3.1) C00003644
354 KLK3, APS, KLK2A1, PSA, hK3 kallikrein-related peptidase 3 (EC:3.4.21.77) C00003644
3972 LHB, CGB4, LSH-B, hLHB luteinizing hormone beta polypeptide C00003644
2475 MTOR, FRAP, FRAP1, FRAP2, RAFT1, RAPT1 mechanistic target of rapamycin (serine/threonine kinase) (EC:2.7.11.1) C00003644
10499 NCOA2, GRIP1, KAT13C, NCoA-2, SRC2, TIF2, bHLHe75 nuclear receptor coactivator 2 C00003644
8202 NCOA3, ACTR, AIB-1, AIB1, CAGH16, CTG26, KAT13B, RAC3, SRC-3, SRC3, TNRC14, TNRC16, TRAM-1, bHLHe42, pCIP nuclear receptor coactivator 3 (EC:2.3.1.48) C00003644
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00003644

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (46)

OMIM preferred title UniProt
#264300 17-beta hydroxysteroid dehydrogenase iii deficiency P37058
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#210900 Bloom syndrome; blm P54132
#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
#114500 Colorectal cancer; crc P84022
#611489 Corticosteroid-binding globulin deficiency P08185
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#615363 Estrogen resistance; estrr P03372
#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
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#613688 Long qt syndrome 2; lqt2 Q12809
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#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
#264600 Pseudovaginal perineoscrotal hypospadias; ppsh P31213
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#609620 Short qt syndrome 1; sqt1 Q12809
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#183090 Spinocerebellar ataxia 2; sca2 Q99700

KEGG DISEASE (32)

KEGG 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)
H00026 Endometrial Cancer P03372 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
P11511 (related)
H01163 Corticosteroid-binding globulin (CBG) deficiency P08185 (related)
H00036 Osteosarcoma P08684 (marker)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
P31213 (related)
P37058 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00794 Aromatase excess syndrome P11511 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000437 Alcoholism C00003644
D002659 Child Development Disorders, Pervasive C00003644