KCF-S cluster No. 1327 (7 metabolites)

Corresponding Phytochemical cluster No. 18


Plant Species


Cumulative plant class count

class name count
rosids 22

Cumulative family count

class name count
Fabaceae 22

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Biflavonoids and polyflavonoids 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Biflavonoids and polyflavonoids C10505 C00002549

Metabolite list (7)

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
C00002549 External link 512 (R)-4-Methoxydalbergione
CHEMBL255297
CHEMBL466581
CHEMBL1554531
18 / 23 / 57
C00010252 External link 512 (S)-4-Methoxydalbergione
CHEMBL255297
CHEMBL466581
CHEMBL1554531
18 / 23 / 57
C00010253 External link 512 (S)-4'-Hydroxy-4-methoxydalbergione
CHEMBL255296
CHEMBL1374504
6 / 4 / 4
C00010254 External link 512 (S)-4,4'-Dimethoxydalbergione
CHEMBL1436980
14 / 11 / 10
C00010255 External link 512 (R)-3,4-Dimethoxydalbergione
CHEMBL1356393
CHEMBL1591258
C026197
16 / 37 / 63
C00010256 External link 512 (R)-4'-Hydroxy-3,4-dimethoxydalbergione
C00010257 External link 512 (S)-3'-Hydroxy-4,4'-dimethoxydalbergione
CHEMBL1801609

Human Protein / Gene in interactions

22 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P16050 Arachidonate 15-lipoxygenase Enzyme C00002549 C00010252 C00010253 C00010254 C00010255 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002549 C00010252 C00010253 C00010254 C00010255 0 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00002549 C00010252 C00010253 C00010254 C00010255 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002549 C00010252 C00010253 C00010254 C00010255 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002549 C00010252 C00010253 C00010254 C00010255 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00002549 C00010252 C00010253 C00010254 C00010255 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00002549 C00010252 C00010254 C00010255 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00002549 C00010252 C00010254 C00010255 2 / 3
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00002549 C00010252 C00010254 C00010255 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002549 C00010252 C00010254 C00010255 1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002549 C00010252 C00010254 C00010255 2 / 2
P04637 Cellular tumor antigen p53 Transcription Factor C00002549 C00010252 C00010255 7 / 37
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002549 C00010252 C00010255 3 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00002549 C00010252 C00010254 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00010254 C00010255 2 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00002549 C00010252 0 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002549 C00010252 1 / 2
O00255 Menin Unclassified protein C00002549 C00010252 2 / 5
Q01196 Runt-related transcription factor 1 Unclassified protein C00002549 C00010252 1 / 4
P02545 Prelamin-A/C Unclassified protein C00010255 11 / 10
P28482 Mitogen-activated protein kinase 1 Erk C00010254 0 / 0
P04062 Glucosylceramidase Enzyme C00010255 6 / 4

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (41)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P18054
#119900 Digital clubbing, isolated congenital P15428
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
P18054
#600274 Frontotemporal dementia; ftd P10636
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#211980 Lung cancer P04637
#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
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#260500 Papilloma of choroid plexus; cpp P04637
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#275210 Restrictive dermopathy, lethal P02545
#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 (71)

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)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (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)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (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)
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)
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)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (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)