KCF-S cluster No. 622 (13 metabolites)

Corresponding Phytochemical cluster No. 2



Metabolite list (13)

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
C00002078 External link 512 Anacrotine
C053598
C00002092 External link 512 Integerrimine
CHEMBL362153
CHEMBL488203
8 / 1 / 5
C00002109 External link 512 Retrorsine
CHEMBL520570
CHEMBL496894
CHEMBL1321908
CHEMBL1599718
C003300
15 / 4 / 9 2 / 0
C00002110 External link 512 Riddelline
C013672
0 / 15
C00002116 External link 512 Senecionine
CHEMBL362153
CHEMBL488203
C009237
8 / 1 / 5 1 / 1
C00002117 External link 512 Seneciphylline
CHEMBL523911
CHEMBL1396368
CHEMBL1439490
CHEMBL1591009
C013678
14 / 12 / 13
C00002118 External link 512 Senecivernine
C00002127 External link 512 Usaramine
CHEMBL520570
CHEMBL496894
CHEMBL1321908
CHEMBL1599718
15 / 4 / 9
C00026179 External link 512 Acetylgynuramine
/ Gynuramine 19-O-acetate
C00026182 External link 512 Seneciphyllinine
/ Acetylseneciphylline
/ O-Acetylseneciphylline
/ Seneciphylline acetate
C066417
C00026183 External link 512 Acetylspartioidine
/ O-Acetylspartioidine
/ Spartioidine acetate
C00026196 External link 512 Gynuramine
/ 19-Hydroxysenecionine
C036949
C00026229 External link 512 Spartioidine
CHEMBL523911
CHEMBL1396368
CHEMBL1439490
CHEMBL1591009
14 / 12 / 13

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q01196 Runt-related transcription factor 1 Unclassified protein C00002092 C00002109 C00002116 C00002117 C00002127 C00026229 1 / 4
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002092 C00002109 C00002116 C00002117 C00002127 C00026229 0 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00002092 C00002109 C00002116 C00002117 C00002127 C00026229 0 / 1
P46063 ATP-dependent DNA helicase Q1 Enzyme C00002092 C00002109 C00002116 C00002117 C00002127 C00026229 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002092 C00002109 C00002116 C00002117 C00002127 C00026229 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00002092 C00002109 C00002116 C00002127 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002109 C00002117 C00002127 C00026229 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002092 C00002116 C00002117 C00026229 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002109 C00002117 C00002127 C00026229 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002109 C00002117 C00002127 C00026229 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002109 C00002117 C00002127 C00026229 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002109 C00002117 C00002127 C00026229 1 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002109 C00002127 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002109 C00002127 0 / 0
P11308 Transcriptional regulator ERG Unclassified protein C00002109 C00002127 1 / 2
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00002117 C00026229 7 / 3
P39748 Flap endonuclease 1 Enzyme C00002092 C00002116 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002117 C00026229 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00002117 C00026229 2 / 3
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002109 C00002127 0 / 0

3 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1557 CYP2C19, CPCJ, CYP2C, P450C2C, P450IIC19 cytochrome P450, family 2, subfamily C, polypeptide 19 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00002109
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) C00002109
54657 UGT1A4, HUG-BR2, UDPGT, UDPGT_1-4, UGT-1D, UGT1-04, UGT1.4, UGT1D UDP glucuronosyltransferase 1 family, polypeptide A4 (EC:2.4.1.17) C00002116

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#612219 Ewing sarcoma; es P11308
#174800 Mccune-albright syndrome; mas P63092
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (15)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H00024 Prostate cancer P11308 (related)
H00035 Ewing's sarcoma P11308 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (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) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)

Diseases related to CTD interactions

16 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D064420 Drug-Related Side Effects and Adverse Reactions C00002116
D000236 Adenoma C00002110
D018248 Adenoma, Liver Cell C00002110
D002471 Cell Transformation, Neoplastic C00002110
D003643 Death C00002110
D004487 Edema C00002110
D006394 Hemangiosarcoma C00002110
D006470 Hemorrhage C00002110
D006965 Hyperplasia C00002110
D007938 Leukemia C00002110
D008113 Liver Neoplasms C00002110
D008114 Liver Neoplasms, Experimental C00002110
D008175 Lung Neoplasms C00002110
D009336 Necrosis C00002110
D010939 Plant Poisoning C00002110
D011654 Pulmonary Edema C00002110