| Organism name | Millettia leucantha |
|---|---|
| Genus | Millettia |
| Family | Fabaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Millettia |
|---|---|
| Linked NCBI taxonomy ID | 53625 |
| Linked level | genus |
| Family in NCBI taxonomy | Fabaceae |
|---|---|
| ID | 3803 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | rosids |
|---|---|
| ID | 71275 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00003997
|
Milleyanaflavone
/ 7-Methoxy-3',4'-methylenedioxyflavone / 2-(1,3-Benzodioxol-5-yl)-7-methoxy-4H-1-benzopyran-4-one |
No. 27 | No. 15 |
|
||||
|
C00005045
|
Demethoxykanugin
/ 2-(1,3-Benzodioxol-5-yl)-3,7-dimethoxy-4H-1-benzopyran-4-one |
CHEMBL2205108
|
No. 27 | No. 15 |
|
|||
|
C00013398
|
3',4'-Methylenedioxy-5,7-dimethoxyflavone
/ 5,7-Dimethoxy-3',4'-methylenedioxyflavone / 2-(1,3-Benzodioxol-5-yl)-5,7-dimethoxy-4H-1-benzopyran-4-one |
No. 27 | No. 15 |
|
||||
|
C00013397
|
5-Hydroxy-7-methoxy-3',4'-methylenedioxyflavone
/ 2-(1,3-Benzodioxol-5-yl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one |
No. 27 | No. 15 |
|
||||
|
C00005089
|
Karanjin
/ 3-Methoxy-2-phenyl-4H-Furo[2,3-h]-1-benzopyran-4-one |
CHEMBL208484
|
C052068
|
20 / 21 / 18 | No. 35 | No. 15 |
|
|
|
C00006977
|
2'-Hydroxy-3,4,4',6'-tetramethoxychalcone
|
CHEMBL243830
|
3 / 3 / 0 | No. 79 |
|
|||
|
C00009741
|
Claussequinone
/ 7-Hydroxy-4'-methoxyisoflavanquinone |
CHEMBL446542
|
C088068
|
No. 517 |
|
|||
|
C00009742
|
Pendulone
/ 7-Hydroxy-3',4'-dimethoxyisoflavanquinone |
No. 517 |
|
|||||
|
C00014439
|
3',4'-Methylenedioxy-2,4,6,beta-tetramethoxychalcone
|
No. 676 |
|
|||||
|
C00014431
|
3,4-Methylenedioxy-2',4',6'-trimethoxychalcone
|
CHEMBL404603
|
No. 676 |
|
||||
|
C00007958
|
Dihydromilletenone methyl ether
|
No. 882 |
|
|||||
|
C00014608
|
2',4',6'-Trimethoxy-3,4-methylenedioxydihydrochalcone
|
No. 882 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00005089 | 1 / 0 |
| P33527 | Multidrug resistance-associated protein 1 | drugs | C00006977 | 0 / 0 |
| P18031 | Tyrosine-protein phosphatase non-receptor type 1 | Tyr | C00005089 | 0 / 0 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00005089 | 0 / 0 |
| P16473 | Thyrotropin receptor | Glycohormone receptor | C00005089 | 3 / 2 |
| P08183 | Multidrug resistance protein 1 | drug | C00006977 | 1 / 0 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00005089 | 0 / 1 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00005089 | 0 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00005089 | 0 / 0 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00005089 | 7 / 3 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00005089 | 0 / 0 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00005089 | 0 / 0 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00005089 | 3 / 3 |
| Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00006977 | 2 / 0 |
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00005089 | 2 / 2 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00005089 | 0 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00005089 | 1 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00005089 | 0 / 1 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00005089 | 4 / 3 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00005089 | 0 / 0 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00005089 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00005089 | 0 / 0 |
| P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00005089 | 0 / 3 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #614490 | Blood group, junior system; jr |
Q9UNQ0
|
| #119900 | Digital clubbing, isolated congenital |
P15428
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #603373 | Hyperthyroidism, familial gestational |
P16473
|
| #609152 | Hyperthyroidism, nonautoimmune |
P16473
|
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
| #275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
| #612244 | Inflammatory bowel disease 13; ibd13 |
P08183
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #166350 | Osseous heteroplasia, progressive; poh |
P63092
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
| #103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
| #603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
| #612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 |
Q9UNQ0
|
| KEGG | name | UniProt |
|---|---|---|
| H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
| H00082 | Graves' disease |
P01215
(marker)
|
| H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
P16473 (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)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
| H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
| H01269 | Congenital hyperthyroidism |
P16473
(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)
|
| 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)
|