Species

KNApSAcK Entry

Organism name Millettia pachycarpa
Genus Millettia
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Millettia pachycarpa
Linked NCBI taxonomy ID 690557
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

Metabolite list (19)

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
C00041676 External link 512 Millewanin H
/ (+)-Millewanin H
CHEMBL523654
1 / 1 / 1 No. 14 No. 15
C00009841 External link 512 6,8-Diprenylpratensein
/ 5,7,3'-Trihydroxy-4'-methoxy-6,8-diprenylisoflavone
No. 14 No. 15
C00041675 External link 512 Millewanin G
/ (+)-Millewanin G
CHEMBL522471
1 / 1 / 1 No. 14 No. 15
C00009516 External link 512 6,8-Diprenylgenistein
/ 8-(gamma,gamma-Dimethylallyl)wighteone
/ 5,7,4'-Trihydroxy-6,8-diprenylisoflavone
CHEMBL494252
12 / 14 / 11 No. 14 No. 15
C00009515 External link 512 Lupalbigenin
/ 5,7,4'-Trihydroxy-6,3'-diprenylisoflavone
CHEMBL463936
No. 14 No. 15
C00009524 External link 512 6,8-Diprenylorobol
/ 5,7,3',4'-Tetrahydroxy-6,8-diprenylisoflavone
No. 14 No. 15
C00003840 External link 512 Salvigenin
CHEMBL376644
C014049
No. 35 No. 15
C00020674 External link 512 2,3-Dihydro-3-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-10-(3-methyl-2-butenyl)-4H,8H-benzol[1,2-b:5,4-b']dipyran-4-one
No. 39
C00008621 External link 512 Lupinifolinol
CHEMBL559586
No. 39
C00041532 External link 512 Furowanin B
/ (+)-Furowanin B
CHEMBL491885
1 / 1 / 1 No. 47 No. 15
C00007063 External link 512 4-Methoxylonchocarpin
CHEMBL369768
No. 130
C00009602 External link 512 Dehydrorotenone
/ Didehydrorotenone
/ 6a,12a-Dehydrorotenone
CHEMBL7940
No. 236 No. 15
C00002537 External link 512 Rotenolone
/ 12a-Hydroxyrotenone
CHEMBL240545
No. 281 No. 15
C00009529 External link 512 1'',2''-Dihydro-8-hydroxyisopentanyl-2'-methoxy-4'-O-methylalpinumisoflavone
No. 724
C00009526 External link 512 1'',2''-Dihydro-2'-hydroxycycloosajin
No. 724
C00009530 External link 512 1'',2''-Dihydro-8-hydroxyisopentanyl-3'-methoxy-4'-O-methylalpinumisoflavone
No. 724
C00009527 External link 512 1'',2''-Dihydro-O-methylcyclopomiferin
No. 724
C00009980 External link 512 cis-12a-Hydroxyrot-2'-enonic acid
No. 765
C00009574 External link 512 Rotenonic acid
CHEMBL2181295
No. 765

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P03372 Estrogen receptor NR3A1 C00041532 C00041675 C00041676 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00009516 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00009516 2 / 0
O75496 Geminin Unclassified protein C00009516 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00009516 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00009516 0 / 0
P04062 Glucosylceramidase Enzyme C00009516 6 / 4
Q99700 Ataxin-2 Unclassified protein C00009516 1 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00009516 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00009516 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00009516 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00009516 1 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00009516 0 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (15)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#137800 Glioma susceptibility 1; glm1 O75874
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (12)

KEGG name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00026 Endometrial Cancer P03372 (marker)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)