Species

KNApSAcK Entry

Organism name Caesalpinia bonduc
Genus Caesalpinia
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Guilandina bonduc
Linked NCBI taxonomy ID 191881
Linked level species

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Natural Activity

List (13)

Species Activity
Caesalpinia bonduc (L.) Roxb. Abortifacient
Caesalpinia bonduc (L.) Roxb. Anthelminthic
Caesalpinia bonduc (L.) Roxb. Antipyretic
Caesalpinia bonduc (L.) Roxb. Antispasmodic
Caesalpinia bonduc (L.) Roxb. Astringent
Caesalpinia bonduc (L.) Roxb. Diuretic
Caesalpinia bonduc (L.) Roxb. Emollient
Caesalpinia bonduc (L.) Roxb. Filaricide
Caesalpinia bonduc (L.) Roxb. Fungicide
Caesalpinia bonduc (L.) Roxb. Hemostat
Caesalpinia bonduc (L.) Roxb. Rubefacient
Caesalpinia bonduc (L.) Roxb. Tonic
Caesalpinia bonduc (L.) Roxb. Vermifuge

Metabolite list (27)

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
C00029388 External link 512 Amarosterol A
/ 13,14-seco-Stigmasta-5,14-dien-3alpha-ol
No. 53 No. 11
C00029389 External link 512 Amarosterol B
/ 13,14-seco-Stigmasta-9(11),14-dien-3alpha-ol
No. 53 No. 11
C00038678 External link 512 Caesalmin D
/ (+)-Caesalmin D
CHEMBL464487
CHEMBL517323
No. 146
C00039137 External link 512 epsilon-Caesalpin
/ (+)-epsilon-Caesalpin
No. 146
C00036857 External link 512 Caesalmin B
/ (+)-Caesalmin B
CHEMBL457149
No. 146
C00029666 External link 512 alpha-Caesalpin
CHEMBL252323
No. 146
C00029836 External link 512 Bonducellpin B
/ (+)-Bonducellpin B
No. 146
C00029837 External link 512 Bonducellpin C
No. 146
C00029880 External link 512 Caesalpinin P
No. 146
C00038618 External link 512 Bonducellpin E
/ (+)-Bonducellpin E
CHEMBL252118
No. 146
C00029870 External link 512 Caesalpinin C
CHEMBL465802
No. 146
C00029873 External link 512 Caesalpinin I
No. 146
C00038620 External link 512 Bonducellpin G
/ (+)-Bonducellpin G
CHEMBL400084
No. 146
C00038619 External link 512 Bonducellpin F
/ (+)-Bonducellpin F
CHEMBL252322
No. 146
C00029869 External link 512 Caesalmin E
/ (+)-Caesalpin H
CHEMBL464487
CHEMBL517323
No. 146
C00029448 External link 512 2-Acetoxycaesaldekarin e
CHEMBL463937
No. 1064
C00010268 External link 512 Brazilin
CHEMBL598951
CHEMBL1370456
C044362
32 / 25 / 25 No. 1670
C00029875 External link 512 Caesalpinin K
/ (+)-Caesalpinin K
No. 1776
C00031643 External link 512 Caesaldekarin A
/ (+)-Caesaldekarin A
No. 1776
C00048341 External link 512 Caesalpinolide C
/ (-)-Caesalpinolide C
No. 2146
C00048343 External link 512 Caesalpinolide E
/ (-)-Caesalpinolide E
CHEMBL514119
No. 2146
C00029868 External link 512 Caesaldekarin J
No. 2729
C00020039 External link 512 Bonducellin
/ (E)-7-Hydroxy-3-(4'-methoxybenzylidene)chroman-4-one
CHEMBL450675
CHEMBL1253830
8 / 25 / 23 No. 2899
C00048342 External link 512 Caesalpinolide D
/ (-)-Caesalpinolide D
No. 3110
C00033244 External link 512 Neocaesalpin C
/ (-)-Neocaesalpin C
No. 3252
C00033245 External link 512 Neocaesalpin D
/ (+)-Neocaesalpin D
No. 3252
C00031033 External link 512 Pipataline
No. 7769

Human Protein / Gene in interactions

40 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00010268 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00010268 2 / 0
P21802 Fibroblast growth factor receptor 2 TK tyrosine-protein kinase TLK subfamily C00020039 9 / 3
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00010268 0 / 0
P14735 Insulin-degrading enzyme Enzyme C00010268 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00010268 3 / 1
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00020039 1 / 8
P11473 Vitamin D3 receptor NR1I1 C00010268 2 / 3
O15296 Arachidonate 15-lipoxygenase B Enzyme C00010268 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00010268 0 / 0
P39748 Flap endonuclease 1 Enzyme C00010268 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00010268 2 / 0
O75496 Geminin Unclassified protein C00010268 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00010268 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00010268 1 / 1
P11308 Transcriptional regulator ERG Unclassified protein C00010268 1 / 2
P83916 Chromobox protein homolog 1 Unclassified protein C00010268 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00010268 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00010268 0 / 0
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00020039 0 / 0
P35968 Vascular endothelial growth factor receptor 2 Vegfr C00020039 1 / 0
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00020039 2 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00010268 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00010268 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00010268 2 / 2
P11362 Fibroblast growth factor receptor 1 Fgfr C00020039 4 / 5
P16050 Arachidonate 15-lipoxygenase Enzyme C00010268 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00010268 0 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00010268 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00010268 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00010268 0 / 0
P10721 Mast/stem cell growth factor receptor Kit Pdgfr C00020039 4 / 3
O14746 Telomerase reverse transcriptase Enzyme C00020039 5 / 5
Q9UBT6 DNA polymerase kappa Enzyme C00010268 0 / 0
Q14145 Kelch-like ECH-associated protein 1 Unclassified protein C00010268 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00010268 0 / 0
O00255 Menin Unclassified protein C00010268 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00010268 1 / 2
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00010268 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00010268 2 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (50)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#207410 Antley-bixler syndrome without genital anomalies or disordered steroidogenesis; abs2 P21802
#101200 Apert syndrome P21802
#609135 Aplastic anemia O14746
#123790 Beare-stevenson cutis gyrata syndrome; bstvs P21802
#614592 Bent bone dysplasia syndrome; bbds P21802
#114500 Colorectal cancer; crc P84022
Q14191
#123500 Crouzon syndrome P21802
#119900 Digital clubbing, isolated congenital P15428
#613989 Dyskeratosis congenita, autosomal dominant, 2; dkca2 O14746
#612219 Ewing sarcoma; es P11308
#600274 Frontotemporal dementia; ftd P10636
#606764 Gastrointestinal stromal tumor; gist P10721
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#602089 Hemangioma, capillary infantile P35968
#114550 Hepatocellular carcinoma P08581
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#147950 Hypogonadotropic hypogonadism 2 with or without anosmia; hh2 P11362
#123150 Jackson-weiss syndrome; jws P21802
#149730 Lacrimoauriculodentodigital syndrome; ladd P21802
#601626 Leukemia, acute myeloid; aml P10721
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P00533
#615134 Melanoma, cutaneous malignant, susceptibility to, 9; cmm9 O14746
#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
#166250 Osteoglophonic dysplasia; ogd P11362
#260540 Parkinson-dementia syndrome P10636
#101600 Pfeiffer syndrome P11362
P21802
#172700 Pick disease of brain P10636
#172800 Piebald trait; pbt P10721
#614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1 O14746
#178500 Pulmonary fibrosis, idiopathic; ipf O14746
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#609579 Scaphocephaly, maxillary retrusion, and mental retardation P21802
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#273300 Testicular germ cell tumor; tgct P10721
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#190440 Trigonocephaly 1; trigno1 P11362
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (47)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00764 Cri du chat syndrome O14746 (related)
H01132 Aplastic anemia (AA) O14746 (related)
H01299 Idiopathic pulmonary fibrosis O14746 (related)
H00022 Bladder cancer O14746 (marker)
P00533 (related)
H00024 Prostate cancer O14746 (marker)
P11308 (related)
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
H00018 Gastric cancer P00533 (related)
P08581 (related)
P21802 (related)
H00028 Choriocarcinoma P00533 (related)
H00030 Cervical cancer P00533 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00021 Renal cell carcinoma P08581 (related)
H00046 Cholangiocarcinoma P08581 (related)
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00003 Acute myeloid leukemia (AML) P10721 (related)
P10721 (marker)
H00170 Piebaldism P10721 (related)
H00023 Testicular cancer P10721 (marker)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00035 Ewing's sarcoma P11308 (related)
H00255 Hypogonadotropic hypogonadism P11362 (related)
H00443 Osteoglophonic dysplasia (OD) P11362 (related)
H00458 Craniosynostosis P11362 (related)
P21802 (related)
H00516 Isolated orofacial clefts P11362 (related)
H01207 Trigonocephaly P11362 (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)
H00642 Lacrimo-auriculo-dento-digital syndrome (LADD) P21802 (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)
H00296 Defects in RecQ helicases Q14191 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)