| Organism name | Caesalpinia bonduc |
|---|---|
| Genus | Caesalpinia |
| Family | Fabaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Guilandina bonduc |
|---|---|
| Linked NCBI taxonomy ID | 191881 |
| Linked level | species |
| Family in NCBI taxonomy | Fabaceae |
|---|---|
| ID | 3803 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | rosids |
|---|---|
| ID | 71275 |
| 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 |
| 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
|
Amarosterol A
/ 13,14-seco-Stigmasta-5,14-dien-3alpha-ol |
No. 53 | No. 11 |
|
||||
|
C00029389
|
Amarosterol B
/ 13,14-seco-Stigmasta-9(11),14-dien-3alpha-ol |
No. 53 | No. 11 |
|
||||
|
C00038678
|
Caesalmin D
/ (+)-Caesalmin D |
CHEMBL464487
CHEMBL517323 |
No. 146 |
|
||||
|
C00039137
|
epsilon-Caesalpin
/ (+)-epsilon-Caesalpin |
No. 146 |
|
|||||
|
C00036857
|
Caesalmin B
/ (+)-Caesalmin B |
CHEMBL457149
|
No. 146 |
|
||||
|
C00029666
|
alpha-Caesalpin
|
CHEMBL252323
|
No. 146 |
|
||||
|
C00029836
|
Bonducellpin B
/ (+)-Bonducellpin B |
No. 146 |
|
|||||
|
C00029837
|
Bonducellpin C
|
No. 146 |
|
|||||
|
C00029880
|
Caesalpinin P
|
No. 146 |
|
|||||
|
C00038618
|
Bonducellpin E
/ (+)-Bonducellpin E |
CHEMBL252118
|
No. 146 |
|
||||
|
C00029870
|
Caesalpinin C
|
CHEMBL465802
|
No. 146 |
|
||||
|
C00029873
|
Caesalpinin I
|
No. 146 |
|
|||||
|
C00038620
|
Bonducellpin G
/ (+)-Bonducellpin G |
CHEMBL400084
|
No. 146 |
|
||||
|
C00038619
|
Bonducellpin F
/ (+)-Bonducellpin F |
CHEMBL252322
|
No. 146 |
|
||||
|
C00029869
|
Caesalmin E
/ (+)-Caesalpin H |
CHEMBL464487
CHEMBL517323 |
No. 146 |
|
||||
|
C00029448
|
2-Acetoxycaesaldekarin e
|
CHEMBL463937
|
No. 1064 |
|
||||
|
C00010268
|
Brazilin
|
CHEMBL598951
CHEMBL1370456 |
C044362
|
32 / 25 / 25 | No. 1670 |
|
||
|
C00029875
|
Caesalpinin K
/ (+)-Caesalpinin K |
No. 1776 |
|
|||||
|
C00031643
|
Caesaldekarin A
/ (+)-Caesaldekarin A |
No. 1776 |
|
|||||
|
C00048341
|
Caesalpinolide C
/ (-)-Caesalpinolide C |
No. 2146 |
|
|||||
|
C00048343
|
Caesalpinolide E
/ (-)-Caesalpinolide E |
CHEMBL514119
|
No. 2146 |
|
||||
|
C00029868
|
Caesaldekarin J
|
No. 2729 |
|
|||||
|
C00020039
|
Bonducellin
/ (E)-7-Hydroxy-3-(4'-methoxybenzylidene)chroman-4-one |
CHEMBL450675
CHEMBL1253830 |
8 / 25 / 23 | No. 2899 |
|
|||
|
C00048342
|
Caesalpinolide D
/ (-)-Caesalpinolide D |
No. 3110 |
|
|||||
|
C00033244
|
Neocaesalpin C
/ (-)-Neocaesalpin C |
No. 3252 |
|
|||||
|
C00033245
|
Neocaesalpin D
/ (+)-Neocaesalpin D |
No. 3252 |
|
|||||
|
C00031033
|
Pipataline
|
No. 7769 |
|
| 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 |
| 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 | 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)
|