Plant Species


Cumulative plant class count

class name count
rosids 3

Cumulative family count

class name count
Meliaceae 2
Burseraceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

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
C00038107 External link 512 (-)-(Z)-Volkendousin
CHEMBL233040
C00039088 External link 512 Ekeberin B
/ (-)-Ekeberin B
C00047241 External link 512 Guggulsterone
CHEMBL372106
CHEMBL402063
CHEMBL410683
CHEMBL1452876
CHEMBL1514005
C023617
41 / 53 / 76 35 / 12

Human Protein / Gene in interactions

41 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00047241 1 / 0
O75469 Nuclear receptor subfamily 1 group I member 2 NR1I2 C00047241 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00047241 7 / 37
Q16637 Survival motor neuron protein Unclassified protein C00047241 4 / 1
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00047241 2 / 2
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00047241 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00047241 3 / 2
P10828 Thyroid hormone receptor beta NR1A2 C00047241 3 / 1
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00047241 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00047241 0 / 1
P54132 Bloom syndrome protein Enzyme C00047241 1 / 2
P11473 Vitamin D3 receptor NR1I1 C00047241 2 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00047241 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00047241 0 / 0
P10145 Interleukin-8 Secreted protein C00047241 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00047241 0 / 1
P06401 Progesterone receptor NR3C3 C00047241 0 / 1
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00047241 5 / 3
Q96RI1 Bile acid receptor NR1H4 C00047241 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00047241 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00047241 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00047241 3 / 3
Q01453 Peripheral myelin protein 22 Unclassified protein C00047241 5 / 2
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00047241 0 / 0
P03372 Estrogen receptor NR3A1 C00047241 1 / 1
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00047241 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00047241 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00047241 0 / 1
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00047241 1 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00047241 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00047241 0 / 0
P08235 Mineralocorticoid receptor NR3C2 C00047241 2 / 2
P10275 Androgen receptor NR3C4 C00047241 3 / 4
P04054 Phospholipase A2 Enzyme C00047241 0 / 0
P40225 Thrombopoietin Unclassified protein C00047241 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00047241 0 / 0
O00255 Menin Unclassified protein C00047241 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00047241 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00047241 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00047241 1 / 4
Q92731 Estrogen receptor beta NR3A2 C00047241 0 / 1

35 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
8647 ABCB11, ABC16, BRIC2, BSEP, PFIC-2, PFIC2, PGY4, SPGP ATP-binding cassette, sub-family B (MDR/TAP), member 11 C00047241
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00047241
597 BCL2A1, ACC-1, ACC-2, BCL2L5, BFL1, GRS, HBPA1 BCL2-related protein A1 C00047241
637 BID, FP497 BH3 interacting domain death agonist C00047241
329 BIRC2, API1, HIAP2, Hiap-2, MIHB, RNF48, c-IAP1, cIAP1 baculoviral IAP repeat containing 2 C00047241
332 BIRC5, API4, EPR-1 baculoviral IAP repeat containing 5 C00047241
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00047241
841 CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) C00047241
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00047241
874 CBR3, SDR21C2, hCBR3 carbonyl reductase 3 (EC:1.1.1.184) C00047241
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00047241
983 CDK1, CDC2, CDC28A, P34CDC2 cyclin-dependent kinase 1 (EC:2.7.11.23 2.7.11.22) C00047241
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00047241
1027 CDKN1B, CDKN4, KIP1, MEN1B, MEN4, P27KIP1 cyclin-dependent kinase inhibitor 1B (p27, Kip1) C00047241
8837 CFLAR, CASH, CASP8AP1, CLARP, Casper, FLAME, FLAME-1, FLAME1, FLIP, I-FLICE, MRIT, c-FLIP, c-FLIPL, c-FLIPR, c-FLIPS CASP8 and FADD-like apoptosis regulator C00047241
1537 CYC1, MC3DN6, UQCR4 cytochrome c-1 C00047241
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00047241
1581 CYP7A1, CP7A, CYP7, CYPVII cytochrome P450, family 7, subfamily A, polypeptide 1 (EC:1.14.13.17) C00047241
2729 GCLC, GCL, GCS, GLCL, GLCLC glutamate-cysteine ligase, catalytic subunit (EC:6.3.2.2) C00047241
2730 GCLM, GLCLR glutamate-cysteine ligase, modifier subunit (EC:6.3.2.2) C00047241
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00047241
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00047241
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00047241
4609 MYC, MRTL, MYCC, bHLHe39, c-Myc v-myc avian myelocytomatosis viral oncogene homolog C00047241
4790 NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 C00047241
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00047241
1728 NQO1, DHQU, DIA4, DTD, NMOR1, NMORI, QR1 NAD(P)H dehydrogenase, quinone 1 (EC:1.6.5.2) C00047241
9971 NR1H4, BAR, FXR, HRR-1, HRR1, RIP14 nuclear receptor subfamily 1, group H, member 4 C00047241
8856 NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR nuclear receptor subfamily 1, group I, member 2 C00047241
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00047241
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00047241
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00047241
7185 TRAF1, EBI6, MGC:10353 TNF receptor-associated factor 1 C00047241
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00047241
331 XIAP, API3, BIRC4, IAP-3, ILP1, MIHA, XLP2, hIAP-3, hIAP3 X-linked inhibitor of apoptosis C00047241

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (53)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#210900 Bloom syndrome; blm P54132
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#118300 Charcot-marie-tooth disease and deafness Q01453
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#133239 Esophageal cancer P04637
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 P37231
#139393 Guillain-barre syndrome, familial; gbs Q01453
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#605115 Hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy P08235
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#145900 Hypertrophic neuropathy of dejerine-sottas Q01453
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P04637
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#601665 Obesity P37231
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#177735 Pseudohypoaldosteronism, type i, autosomal dominant; pha1a P08235
#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
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#187950 Thrombocythemia 1; thcyt1 P40225
#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
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (76)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00026 Endometrial Cancer P03372 (marker)
P04637 (related)
P06401 (marker)
Q92731 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00243 Hyperkalemic distal renal tubular acidosis (RTA type 4) P08235 (related)
H00603 Hypertension exacerbated in pregnancy P08235 (related)
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)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00227 Congenital amegakaryocytic thrombocytopenia (CAMT) P40225 (marker)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00264 Charcot-Marie-Tooth disease (CMT) Q01453 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (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

12 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D050197 Atherosclerosis C00047241
D001943 Breast Neoplasms C00047241
D002283 Carcinoma, Bronchogenic C00047241
C535575 Carcinoma, squamous cell of head and neck C00047241
D003920 Diabetes Mellitus C00047241
D006949 Hyperlipidemias C00047241
D007938 Leukemia C00047241
D008545 Melanoma C00047241
D009101 Multiple Myeloma C00047241
D009765 Obesity C00047241
D010003 Osteoarthritis C00047241
D010051 Ovarian Neoplasms C00047241