KCF-S cluster No. 323 (21 metabolites)

Corresponding Phytochemical cluster No. 41


KEGG BRITE br08003 External link 512


Categories (2)

br08003 Category # of metabolite
Others 1
Podocarpanes 2

metabolites link (3)

br08003 Category KEGG ID KNApSAcK ID
Others C09163 C00003470
Podocarpanes C09171 C00003474
Podocarpanes C12078 C00042455

Metabolite list (21)

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
C00003470 External link 512 Pisiferic acid
C060710
C00003474 External link 512 Podocarpic acid
CHEMBL421115
CHEMBL2220581
C002470
8 / 4 / 1
C00029387 External link 512 12-O-methylcarnosic acid
/ 12-O-Methyl carnosic acid
/ (+)-12-O-Methyl carnosic acid
/ Carnosic acid 12-methyl ether
CHEMBL1096627
C00029401 External link 512 15-Hydroxydehydroabietic acid
CHEMBL598566
CHEMBL1348397
6 / 8 / 4
C00029523 External link 512 4beta-Carboxy-19-nortotarol
CHEMBL517672
C00030622 External link 512 Lambertic acid
/ (+)-Lambertic acid
CHEMBL519807
CHEMBL523920
1 / 1 / 1
C00034400 External link 512 7-Oxo-15-hydroxydehydroabietic acid
CHEMBL597920
C00035978 External link 512 7-Oxodehydroabietic acid
/ 7-Ketodehydroabietic acid
CHEMBL597919
C095375
1 / 1 / 1
C00036186 External link 512 O-Methylpisiferic acid
CHEMBL479111
C00036880 External link 512 Carnosic acid
CHEMBL484853
CHEMBL1397655
C018381
17 / 23 / 55 6 / 4
C00040763 External link 512 12,15-Dihydroxyabieta-8,11,13-trien-18-oic acid
C00040773 External link 512 16-nor-15-Oxoabieta-8,11,13-trien-18-oic acid
C00040858 External link 512 Abieta-8,11,13,15-tetraen-18-oic acid
C00042455 External link 512 Dehydroabietic acid
CHEMBL12850
C013913
C00046986 External link 512 12-Hydroxydehydroabietic acid
/ (+)-12-Hydroxydehydroabietic acid
CHEMBL519807
CHEMBL523920
1 / 1 / 1
C00047642 External link 512 15-Hydroxy-6-en-dehydroabietic acid
/ (-)-15-Hydroxy-6-en-dehydroabietic acid
C00048932 External link 512 16-Hydroxycarnosic acid
C00049963 External link 512 7beta-Hydroxyabieta-8,11,13-trien-18-oic acid
/ (+)-7beta-Hydroxyabieta-8,11,13-trien-18-oic acid
CHEMBL604665
CHEMBL604787
C00049984 External link 512 Angustanoic acid F
CHEMBL598566
CHEMBL1348397
6 / 8 / 4
C00049989 External link 512 Angustanoic acid E
C00049990 External link 512 Angustanoic acid G
/ (+)-Angustanoic acid G

Human Protein / Gene in interactions

31 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q12791 Calcium-activated potassium channel subunit alpha-1 KCNM, KCa1.x C00003474 C00030622 C00035978 C00046986 1 / 1
P06746 DNA polymerase beta Enzyme C00029401 C00049984 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00029401 C00049984 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00029401 C00049984 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00029401 C00049984 1 / 1
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00029401 C00049984 7 / 3
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00029401 C00049984 0 / 0
P55055 Oxysterols receptor LXR-beta NR1H3 C00003474 0 / 0
P16233 Pancreatic triacylglycerol lipase Hydrolase C00036880 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00036880 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00036880 2 / 3
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00036880 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00036880 2 / 0
Q13133 Oxysterols receptor LXR-alpha NR1H3 C00003474 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00036880 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme 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
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003474 2 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00036880 7 / 37
P10636 Microtubule-associated protein tau Unclassified protein C00036880 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00036880 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00036880 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00036880 1 / 1
O00255 Menin Unclassified protein C00036880 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00036880 1 / 2
Q15118 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 1, mitochondrial Pdhk C00003474 0 / 0
Q16654 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 4, mitochondrial Pdhk C00003474 0 / 0
Q15119 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 2, mitochondrial Pdhk C00003474 0 / 0
Q15120 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 3, mitochondrial Pdhk C00003474 1 / 0

6 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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (35)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#300905 Charcot-marie-tooth disease, x-linked dominant, 6; cmtx6 Q15120
#114500 Colorectal cancer; crc P18054
#119900 Digital clubbing, isolated congenital P15428
#133239 Esophageal cancer P04637
P18054
#600274 Frontotemporal dementia; ftd P10636
#609446 Generalized epilepsy and paroxysmal dyskinesia; gepd Q12791
#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
#211980 Lung cancer P04637
#174800 Mccune-albright syndrome; mas P63092
#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
#166350 Osseous heteroplasia, progressive; poh P63092
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#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
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (60)

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)
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)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (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)
H01258 Generalized epilepsy and paroxysmal dyskinesia (GEPD) Q12791 (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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (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