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
![]() |
Carnosic acid
|
CHEMBL484853
CHEMBL1397655 |
C018381
|
17 / 23 / 55 | 6 / 4 | No. 323 | No. 41 |
![]() |
C00003410
![]() |
Carnosol
|
CHEMBL218693
CHEMBL1514916 |
C068623
|
17 / 17 / 17 | 12 / 0 | No. 734 | No. 40 |
![]() |
C00031191
![]() |
Rosmanol
|
No. 734 | No. 40 |
![]() |
||||
C00037344
![]() |
Isorosmanol
|
CHEMBL494659
CHEMBL2333536 |
No. 734 | No. 40 |
![]() |
|||
C00044167
![]() |
Ethylrosmanol
|
CHEMBL464584
CHEMBL1986643 |
No. 734 | No. 40 |
![]() |
|||
C00044118
![]() |
Carnosic acid methyl ester
|
CHEMBL2333537
|
No. 2322 |
![]() |
||||
C00044155
![]() |
Epimethylrosmanol
|
No. 4516 |
![]() |
|||||
C00044154
![]() |
Epiethylrosmanol
/ (+)-Epiethylrosmanol |
No. 4516 |
![]() |
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 |
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
|
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 | 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)
|