Species

KNApSAcK Entry

Organism name Murraya paniculata
Genus Murraya
Family Rutaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Murraya paniculata
Linked NCBI taxonomy ID 43711
Linked level species

Family

Family in NCBI taxonomy Rutaceae
ID 23513

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (35)

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
C00013340 External link 512 5,3',5'-Trihydroxy-6,7,4'-trimethoxyflavone
/ 2-(3,5-Dihydroxy-4-methoxyphenyl)-5-hydroxy-6,7-dimethoxy-4H-1-benzopyran-4-one
No. 3 No. 15
C00003918 External link 512 5,7,3',4',5'-Pentamethoxyflavone
/ Tricetin 5,7,3',4',5'-pentamethyl ether
/ 5,7-Dimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL2074901
1 / 1 / 0 No. 8 No. 15
C00003936 External link 512 Demethylnobiletin
/ 5-Hydroxy-6,7,8,3',4'-pentamethoxyflavone
/ 2-(3,4-Dimethoxyphenyl)-5-hydroxy-6,7,8-trimethoxy-4H-1-benzopyran-4-one
CHEMBL75978
21 / 22 / 16 No. 8 No. 15
C00003947 External link 512 5,3'-Dihydroxy-6,7,4',5'-tetramethoxyflavone
/ 5-Hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-6,7-dimethoxy-4H-1-benzopyran-4-one
No. 8 No. 15
C00003949 External link 512 Umuhengerin
/ 5-Hydroxy-6,7,3',4',5'-pentamethoxyflavone
/ 5-Hydroxy-6,7-dimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL485823
C057913
No. 8 No. 15
C00003962 External link 512 Bannamurpanisin
No. 8 No. 15
C00003970 External link 512 Gardenin E
/ 3',5,5'-Trihydroxy-4',6,7,8-tetramethoxyflavone
/ 2-(3,5-Dihydroxy-4-methoxyphenyl)-5-hydroxy-6,7,8-trimethoxy-4H-1-benzopyran-4-one
No. 8 No. 15
C00003972 External link 512 Gardenin C
/ 3',5-Dihydroxy-4',5',6,7,8-pentamethoxyflavon
/ 5-Hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-6,7,8-trimethoxy-4H-1-benzopyran-4-one
No. 8 No. 15
C00003976 External link 512 Gardenin A
/ 5-Hydroxy-3',4',5',6,7,8-hexamethoxyflavone
/ 5-Hydroxy-6,7,8-trimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL77705
21 / 18 / 8 No. 8 No. 15
C00004082 External link 512 5,6,7,3',4',5'-Hexamethoxyflavone
/ 5,6,7-Trimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL370963
1 / 1 / 0 No. 8 No. 15
C00004744 External link 512 Gossypetin 3,7,8,3',4'-pentamethyl ether
/ 5-Hydroxy-3,7,8,3',4'-pentamethoxyflavone
/ 2-(3,4-Dimethoxyphenyl)-5-hydroxy-3,7,8-trimethoxy-4H-1-benzopyran-4-one
CHEMBL479326
No. 8 No. 15
C00013381 External link 512 8-Hydroxy-3,5,7,3',4',5'-hexamethoxyflavone
/ 8-Hydroxy-3,5,7-trimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one
No. 8 No. 15
C00004778 External link 512 Hexamethylmyricetin
/ Hexa-O-methylmyricitin
/ Myricetin hexamethyl ether
/ 3,5,7,3',4',5'-Hexamethoxyflavone
/ 3,5,7-Trimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL357089
1 / 0 / 0 No. 8 No. 15
C00004835 External link 512 4'-Hydroxy-3,5,6,7,3',5'-hexamethoxyflavone
No. 8 No. 15
C00004836 External link 512 5-Hydroxy-3,6,7,3',4',5'-hexamethoxyflavone
/ 5-Hydroxy-3,6,7-trimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-Benzopyran-4-one
No. 8 No. 15
C00004837 External link 512 3,5,6,7,3',4',5'-Heptamethoxyflavone
/ 3,5,6,7-Tetramethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one
No. 8 No. 15
C00004847 External link 512 Hibiscetin heptamethyl ether
No. 8 No. 15
C00013382 External link 512 5-Hydroxy-3,3',4',5',7,8-hexamethoxyflavone
/ 5-Hydroxy-3,7,8-trimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one
No. 8 No. 15
C00013373 External link 512 3-Hydroxy-5,7,3',4',5'-pentamethoxyflavone
/ 3-Hydroxy-5,7-dimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one
No. 8 No. 15
C00004745 External link 512 Gossypetin hexamethyl ether
/ 3,5,7,8,3',4'-Hexamethoxyflavone
/ 2-(3,4-Dimethoxyphenyl)-3,5,7,8-tetramethoxy-4H-1-benzopyran-4-one
No. 8 No. 15
C00019970 External link 512 Murrayacarpin B
No. 364 No. 25
C00019812 External link 512 Chloculol
No. 1039
C00019966 External link 512 Murracarpin
No. 1039
C00037493 External link 512 Meranzin hydrate
/ (-)-Meranzin hydrate
CHEMBL433093
2 / 0 / 0 No. 1726
C00019969 External link 512 Murrayacarpin A
No. 1814
C00019968 External link 512 Murralonginol isovalerate
No. 1945
C00019994 External link 512 Paniculonol isovalerate
No. 1945
C00019936 External link 512 Isomurralonginol isovalerate
No. 1945
C00026590 External link 512 Paniculidine C
No. 2298
C00026589 External link 512 Paniculidine B
No. 2298
C00019967 External link 512 Murraculatin
No. 3868
C00019987 External link 512 Omphalocarpin
No. 3868
C00019974 External link 512 Murrayanone
No. 4290
C00000490 External link 512 Yuehchukene
C047409
No. 5887
C00029074 External link 512 Tamynine
No. 7142

Human Protein / Gene in interactions

29 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9BVA1 Tubulin beta-2B chain Structural C00003936 C00003976 1 / 0
Q9BUF5 Tubulin beta-6 chain Structural C00003936 C00003976 0 / 0
Q9BQE3 Tubulin alpha-1C chain Unclassified protein C00003936 C00003976 0 / 0
Q6PEY2 Tubulin alpha-3E chain Unclassified protein C00003936 C00003976 0 / 0
P08183 Multidrug resistance protein 1 drug C00003918 C00004082 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00003936 C00003976 0 / 0
Q13885 Tubulin beta-2A chain Structural C00003936 C00003976 0 / 0
P68363 Tubulin alpha-1B chain Unclassified protein C00003936 C00003976 0 / 0
Q13509 Tubulin beta-3 chain Structural C00003936 C00003976 2 / 1
P68371 Tubulin beta-4B chain Structural C00003936 C00003976 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003936 C00003976 0 / 1
Q71U36 Tubulin alpha-1A chain Structural C00003936 C00003976 1 / 1
P07437 Tubulin beta chain Structural C00003936 C00003976 0 / 0
Q3ZCM7 Tubulin beta-8 chain Structural C00003936 C00003976 0 / 0
P04350 Tubulin beta-4A chain Structural C00003936 C00003976 2 / 0
P68366 Tubulin alpha-4A chain Structural C00003936 C00003976 0 / 0
Q9H4B7 Tubulin beta-1 chain Structural C00003936 C00003976 1 / 0
Q13748 Tubulin alpha-3C/D chain Structural C00003936 C00003976 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00037493 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00003976 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00003936 4 / 3
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00003976 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00003936 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00037493 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00003976 7 / 3
P37840 Alpha-synuclein Unclassified protein C00003976 4 / 2
P02545 Prelamin-A/C Unclassified protein C00003936 11 / 10
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00003936 0 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00004778 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (34)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#614039 Cortical dysplasia, complex, with other brain malformations 1; cdcbm1 Q13509
#127750 Dementia, lewy body; dlb P37840
#128101 Dystonia 4, torsion, autosomal dominant; dyt4 P04350
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#600638 Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement; cfeom3a Q13509
#600274 Frontotemporal dementia; ftd P10636
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#612244 Inflammatory bowel disease 13; ibd13 P08183
#612438 Leukodystrophy, hypomyelinating, 6; hld6 P04350
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#611603 Lissencephaly 3; lis3 Q71U36
#613112 Macrothrombocytopenia, autosomal dominant, tubb1-related Q9H4B7
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#166350 Osseous heteroplasia, progressive; poh P63092
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#610031 Polymicrogyria, symmetric or asymmetric; pmgysa Q9BVA1
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#275210 Restrictive dermopathy, lethal P02545
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (21)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (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)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00838 Congenital fibrosis of the extraocular muscles (CFEOM) Q13509 (related)
H00268 Lissencephaly (LIS) Q71U36 (related)