Species

KNApSAcK Entry

Organism name Croton zambesicus
Genus Croton
Family Euphorbiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Croton zambesicus
Linked NCBI taxonomy ID 323089
Linked level species

Family

Family in NCBI taxonomy Euphorbiaceae
ID 3977

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (15)

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
C00003737 External link 512 alpha-Amyrin
/ alpha-Amyrine
/ alpha-Amyrenol
No. 23 No. 51
C00003749 External link 512 Lupeol
/ Lupenol
/ (+)-Lupenol
CHEMBL289191
CHEMBL459702
C010480
3 / 0 / 0 2 / 6 No. 23 No. 51
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00023770 External link 512 Sitosterol
/ Stigmasta-5,22-dien-3beta-ol
/ (24R)24-Ethylcholesta-5,22-dien-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00003674 External link 512 Stigmasterol
/ beta-Stigmasterol
CHEMBL66943
CHEMBL186373
CHEMBL400247
CHEMBL1568947
D013265
5 / 0 / 0 1 / 0 No. 53 No. 11
C00034864 External link 512 Isopimara-7,15-dien-3beta-ol
/ (-)-Isopimara-7,15-dien-3beta-ol
CHEMBL225866
No. 208 No. 48
C00038866 External link 512 Crotonadiol
/ (+)-Crotonadiol
No. 347
C00003467 External link 512 Phytol
/ trans-Phytol
CHEMBL390773
CHEMBL1644111
D010836
0 / 5 No. 641 No. 38
C00036945 External link 512 Crotozambefuran C
/ (-)-Crotozambefuran C
No. 731
C00036942 External link 512 Crotocorylifuran
/ (-)-Crotocorylifuran
No. 731
C00036943 External link 512 Crotozambefuran A
/ (-)-Crotozambefuran A
No. 731
C00037924 External link 512 Trachyloban-7beta,18-diol
No. 2921
C00035605 External link 512 ent-Trachyloban-3-one
CHEMBL461825
No. 2921
C00036644 External link 512 7beta-Acetoxytrachyloban-18-oic acid
CHEMBL497899
No. 4025
C00036944 External link 512 Crotozambefuran B
/ (-)-Crotozambefuran B
No. 7136

Human Protein / Gene in interactions

22 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P06746 DNA polymerase beta Enzyme C00003672 C00003674 C00023770 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00003672 C00003749 C00023770 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003672 C00023770 0 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003672 C00023770 1 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00003672 C00023770 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00003672 C00023770 3 / 2
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003672 C00023770 1 / 1
P08183 Multidrug resistance protein 1 drug C00003672 C00023770 1 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 C00023770 2 / 0
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 C00023770 1 / 1
P11388 DNA topoisomerase 2-alpha Isomerase C00003674 C00003749 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003672 C00023770 1 / 1
P00734 Prothrombin S1A C00003672 C00023770 4 / 2
P14679 Tyrosinase Oxidoreductase C00003672 C00023770 4 / 2
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003672 C00023770 0 / 0
P03372 Estrogen receptor NR3A1 C00003672 C00023770 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003672 C00023770 0 / 1
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 C00023770 0 / 0
P09884 DNA polymerase alpha catalytic subunit Transferase C00003674 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00003749 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00003674 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00003674 0 / 0

3 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1499 CTNNB1, CTNNB, MRD19, armadillo catenin (cadherin-associated protein), beta 1, 88kDa C00003749
5728 PTEN, 10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC1, PTEN1, TEP1 phosphatase and tensin homolog (EC:3.1.3.67 3.1.3.16 3.1.3.48) C00003749
10599 SLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 solute carrier organic anion transporter family, member 1B1 C00003674

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (19)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#218030 Apparent mineralocorticoid excess; ame P80365
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#615363 Estrogen resistance; estrr P03372
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734

KEGG DISEASE (12)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00026 Endometrial Cancer P03372 (marker)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

11 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006528 Carcinoma, Hepatocellular C00003749
D009202 Cardiomyopathies C00003749
D006937 Hypercholesterolemia C00003749
D009374 Neoplasms, Experimental C00003749
D012878 Skin Neoplasms C00003749
D014947 Wounds and Injuries C00003749
D056486 Drug-Induced Liver Injury C00003467
D006965 Hyperplasia C00003467
D006984 Hypertrophy C00003467
D009336 Necrosis C00003467
D015431 Weight Loss C00003467