Species

KNApSAcK Entry

Organism name Hypis dilatata
Genus
Family
Kingdom

Metabolite list (8)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00036880 External link 512 Carnosic acid
CHEMBL484853
CHEMBL1397655
C018381
17 / 23 / 55 6 / 4 No. 323 No. 41
C00003410 External link 512 Carnosol
CHEMBL218693
CHEMBL1514916
C068623
17 / 17 / 17 12 / 0 No. 734 No. 40
C00031191 External link 512 Rosmanol
No. 734 No. 40
C00037344 External link 512 Isorosmanol
CHEMBL494659
CHEMBL2333536
No. 734 No. 40
C00044167 External link 512 Ethylrosmanol
CHEMBL464584
CHEMBL1986643
No. 734 No. 40
C00044118 External link 512 Carnosic acid methyl ester
CHEMBL2333537
No. 2322
C00044155 External link 512 Epimethylrosmanol
No. 4516
C00044154 External link 512 Epiethylrosmanol
/ (+)-Epiethylrosmanol
No. 4516

Human Protein / Gene in interactions

29 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003410 C00036880 1 / 2
O00255 Menin Unclassified protein C00003410 C00036880 2 / 5
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00003410 C00036880 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00003410 C00036880 2 / 3
P16233 Pancreatic triacylglycerol lipase Hydrolase C00003410 C00036880 0 / 0
P37840 Alpha-synuclein Unclassified protein C00003410 4 / 2
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00036880 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00036880 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00036880 0 / 0
P39748 Flap endonuclease 1 Enzyme C00003410 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00003410 0 / 0
P11413 Glucose-6-phosphate 1-dehydrogenase Enzyme C00003410 1 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00003410 2 / 0
O75496 Geminin Unclassified protein C00003410 0 / 0
Q9Y5X4 Photoreceptor-specific nuclear receptor NR2E3 C00003410 2 / 2
P83916 Chromobox protein homolog 1 Unclassified protein C00003410 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00003410 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00036880 2 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00036880 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00036880 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00036880 2 / 2
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00036880 0 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00003410 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00036880 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00036880 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003410 2 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00036880 1 / 1
Q99700 Ataxin-2 Unclassified protein C00003410 1 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00036880 7 / 37

18 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
100136148 C00036880
929 CD14 CD14 molecule C00036880
5468 PPARG, CIMT1, GLM1, NR1C3, PPARG1, PPARG2, PPARgamma peroxisome proliferator-activated receptor gamma C00036880
5914 RARA, NR1B1, RAR retinoic acid receptor, alpha C00036880
6256 RXRA, NR2B1 retinoid X receptor, alpha C00036880
7421 VDR, NR1I1 vitamin D (1,25- dihydroxyvitamin D3) receptor C00036880
196 AHR, bHLHe76 aryl hydrocarbon receptor C00003410
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00003410
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00003410
2729 GCLC, GCL, GCS, GLCL, GLCLC glutamate-cysteine ligase, catalytic subunit (EC:6.3.2.2) C00003410
2730 GCLM, GLCLR glutamate-cysteine ligase, modifier subunit (EC:6.3.2.2) C00003410
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00003410
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00003410
3551 IKBKB, IKK-beta, IKK2, IKKB, NFKBIKB inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta (EC:2.7.11.10) C00003410
4780 NFE2L2, NRF2 nuclear factor, erythroid 2-like 2 C00003410
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00003410
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00003410
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00003410

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (34)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#300908 Anemia, nonspherocytic hemolytic, due to g6pd deficiency P11413
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#114500 Colorectal cancer; crc P18054
P84022
#127750 Dementia, lewy body; dlb P37840
#119900 Digital clubbing, isolated congenital P15428
#268100 Enhanced s-cone syndrome; escs Q9Y5X4
#133239 Esophageal cancer P04637
P18054
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#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
#260500 Papilloma of choroid plexus; cpp P04637
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#611131 Retinitis pigmentosa 37; rp37 Q9Y5X4
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (61)

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)
H00004 Chronic myeloid leukemia (CML) P04637 (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)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00101 Other phagocyte defects P11413 (related)
H00668 Anemia due to disorders of glutathione metabolism P11413 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (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)
H00527 Retinitis pigmentosa (RP) Q9Y5X4 (related)
H00805 Vitreoretinal degeneration Q9Y5X4 (related)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D002294 Carcinoma, Squamous Cell C00036880
D006965 Hyperplasia C00036880
D009062 Mouth Neoplasms C00036880
D009374 Neoplasms, Experimental C00036880