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)
|