Organism name | Marrubium vulgare |
---|---|
Genus | Marrubium |
Family | Labiatae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Marrubium vulgare |
---|---|
Linked NCBI taxonomy ID | 41230 |
Linked level | species |
Family in NCBI taxonomy | Lamiaceae |
---|---|
ID | 4136 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | asterids |
---|---|
ID | 71274 |
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 |
---|---|---|---|---|---|---|---|---|
C00004316
![]() |
Luteolin 7-(6''-acetylglucoside)
|
No. 2 | No. 15 |
![]() |
||||
C00004322
![]() |
Luteolin 7-(2''-glucuronosyllactate)
|
No. 2 | No. 15 |
![]() |
||||
C00004321
![]() |
Luteolin 7-(2''-glucosyllactate)
|
No. 2 | No. 15 |
![]() |
||||
C00004182
![]() |
Apigenin 7-(2''-glucuronosyllactate)
|
No. 2 | No. 15 |
![]() |
||||
C00004181
![]() |
Apigenin 7-(2''-glucosyllactate)
|
No. 2 | No. 15 |
![]() |
||||
C00036138
![]() |
Marruboside
/ (-)-Marruboside |
No. 33 |
![]() |
|||||
C00036042
![]() |
Ballotetroside
|
No. 33 |
![]() |
|||||
C00023321
![]() |
Vulgarol
|
CHEMBL589839
CHEMBL1644112 |
No. 118 | No. 46 |
![]() |
|||
C00003476
![]() |
(13R)-Premarrubiin
|
C105732
|
No. 689 | No. 41 |
![]() |
|||
C00023347
![]() |
(13S)-Premarrubiin
|
No. 689 | No. 41 |
![]() |
||||
C00003452
![]() |
Marrubiin
|
CHEMBL1444915
CHEMBL1999372 |
C105731
|
5 / 1 / 4 | No. 874 | No. 41 |
![]() |
|
C00022294
![]() |
Marrubenol
|
CHEMBL389065
|
No. 1134 |
![]() |
||||
C00004180
![]() |
Apigenin 7-lactate
|
No. 2389 |
![]() |
|||||
C00004320
![]() |
Luteolin 7-lactate
|
No. 2389 |
![]() |
|||||
C00001345
![]() |
(-)-Betonicine
/ 4-Hydroxyproline betaine |
CHEMBL1181451
CHEMBL1373466 CHEMBL1996398 |
7 / 16 / 14 | No. 2627 | No. 1 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001345 | 1 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00001345 | 11 / 10 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00001345 | 3 / 1 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001345 | 0 / 1 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00003452 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001345 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003452 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001345 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001345 | 0 / 1 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00003452 | 0 / 0 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00003452 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00003452 | 1 / 4 |
OMIM | preferred title | UniProt |
---|---|---|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#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
|
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)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|