Organism name | Phlomis spinidens |
---|---|
Genus | Phlomis |
Family | Labiatae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Phlomis |
---|---|
Linked NCBI taxonomy ID | 316257 |
Linked level | genus |
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 |
---|---|---|---|---|---|---|---|---|
C00033294
![]() |
Phlomisflavoside B
/ (-)-Phlomisflavoside B |
No. 1 | No. 15 |
![]() |
||||
C00033293
![]() |
Phlomisflavoside A
/ (-)-Phlomisflavoside A |
No. 1 | No. 15 |
![]() |
||||
C00005373
![]() |
Hirsutrin
/ Isoquercetin / Isoquercetrin / (-)-Isoquercetrin / Quercetin 3-glucoside / Quercetin 3-O-beta-D-glucoside / Quercetin-3-O-beta-D-glucopyranoside / Quercetin 3-O-beta-D-glucopyranoside / (-)-Quercetin-3-O-beta-D-glucopyranoside |
CHEMBL33027
CHEMBL309323 CHEMBL250450 CHEMBL251254 CHEMBL457304 CHEMBL1098724 CHEMBL2337335 CHEMBL2337336 |
38 / 43 / 34 | No. 2 | No. 15 |
![]() |
||
C00005138
![]() |
Astragalin
/ Kaempferol 3-glucoside / Kaempferol 3-O-beta-D-glucoside / Kaempferol 3-O-beta-D-glucopyranoside |
CHEMBL233930
CHEMBL453290 CHEMBL1572115 |
C001579
|
10 / 6 / 7 | 0 / 1 | No. 2 | No. 15 |
![]() |
C00030317
![]() |
Forsythoside B
|
CHEMBL393292
|
1 / 0 / 3 | No. 33 |
![]() |
|||
C00031274
![]() |
Salidroside
/ Rhodioloside / (-)-Rhodioloside / Tyrosol alpha-(beta-D-glucopyranoside) |
CHEMBL465208
CHEMBL1899113 |
C009172
|
3 / 0 / 0 | No. 45 | No. 72 |
![]() |
|
C00010690
![]() |
Barlerin
/ (-)-Barlerin / 8-O-Acetylshanzhiside methyl ester |
CHEMBL463751
CHEMBL463377 |
C099473
|
No. 56 | No. 36 |
![]() |
||
C00033295
![]() |
Phlomoside A
/ (-)-Phlomoside A |
No. 56 | No. 36 |
![]() |
||||
C00010687
![]() |
Shanzhiside methyl ester
|
CHEMBL1081414
|
1 / 1 / 1 | No. 56 | No. 36 |
![]() |
||
C00010589
![]() |
Lamalbid
/ Lamalbide / Lamiridoside |
CHEMBL1079619
CHEMBL2048642 |
No. 56 | No. 36 |
![]() |
|||
C00033296
![]() |
Phlorigidoside C
/ (-)-Phlorigidoside C |
CHEMBL2048531
|
No. 56 | No. 36 |
![]() |
|||
C00029980
![]() |
Citroside A
/ (-)-Citroside A |
CHEMBL1814429
|
No. 316 |
![]() |
||||
C00000602
![]() |
(+)-Lariciresinol
|
CHEMBL518421
|
2 / 1 / 1 | No. 700 | No. 21 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9Y253 | DNA polymerase eta | Enzyme | C00005138 C00005373 | 1 / 1 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00005138 C00005373 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00005138 C00005373 | 0 / 0 |
P14679 | Tyrosinase | Oxidoreductase | C00005138 C00005373 | 4 / 2 |
P15121 | Aldose reductase | Enzyme | C00005138 C00005373 | 0 / 0 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00005373 C00030317 | 0 / 3 |
O75496 | Geminin | Unclassified protein | C00005373 C00031274 | 0 / 0 |
P07237 | Protein disulfide-isomerase | Enzyme | C00005138 C00005373 | 0 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00000602 | 1 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00005138 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00005373 | 11 / 10 |
P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | C00005373 | 1 / 1 |
P18825 | Alpha-2C adrenergic receptor | Adrenergic receptor | C00005373 | 0 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00005373 | 6 / 4 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00005373 | 1 / 0 |
P60033 | CD81 antigen | Unclassified protein | C00010687 | 1 / 1 |
P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00031274 | 0 / 0 |
P41145 | Kappa-type opioid receptor | Opioid receptor | C00005373 | 0 / 0 |
P36888 | Receptor-type tyrosine-protein kinase FLT3 | Pdgfr | C00005373 | 1 / 1 |
P39748 | Flap endonuclease 1 | Enzyme | C00005373 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00005373 | 0 / 0 |
P41143 | Delta-type opioid receptor | Opioid receptor | C00005373 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00005138 | 1 / 1 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00005373 | 1 / 1 |
P09923 | Intestinal-type alkaline phosphatase | Enzyme | C00005373 | 0 / 0 |
P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | Enzyme | C00005373 | 3 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00031274 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00005373 | 0 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00005373 | 1 / 1 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00005373 | 0 / 0 |
P10696 | Alkaline phosphatase, placental-like | Enzyme | C00005373 | 0 / 1 |
Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00005373 | 2 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00005138 | 0 / 0 |
P35372 | Mu-type opioid receptor | Opioid receptor | C00005373 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00000602 | 0 / 1 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00005373 | 4 / 1 |
Q9NPH5 | NADPH oxidase 4 | Enzyme | C00005373 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00005373 | 4 / 3 |
P08908 | 5-hydroxytryptamine receptor 1A | Serotonin receptor | C00005373 | 1 / 0 |
P34949 | Mannose-6-phosphate isomerase | Enzyme | C00005373 | 1 / 1 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00005373 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00005373 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00005373 | 0 / 0 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00005373 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00005373 | 1 / 4 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00005373 | 0 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00005138 | 0 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
#203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
#606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
#614490 | Blood group, junior system; jr |
Q9UNQ0
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#602579 | Congenital disorder of glycosylation, type ib; cdg1b |
P34949
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#301500 | Fabry disease |
P06280
|
#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
|
#232300 | Glycogen storage disease ii |
P10253
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#146300 | Hypophosphatasia, adult |
P05186
|
#241510 | Hypophosphatasia, childhood |
P05186
|
#241500 | Hypophosphatasia, infantile |
P05186
|
#613496 | Immunodeficiency, common variable, 6; cvid6 |
P60033
|
#601626 | Leukemia, acute myeloid; aml |
P36888
|
#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
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#614674 | Periodic fever, menstrual cycle-dependent |
P08908
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
#253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
#253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
#253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
#271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 |
Q9UNQ0
|
#278300 | Xanthinuria, type i |
P47989
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
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)
|
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)
|
H00213 | Hypophosphatasia |
P05186
(related)
|
H00125 | Fabry disease |
P06280
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00023 | Testicular cancer |
P10696
(marker)
|
H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
H00038 | Malignant melanoma |
P14679
(marker)
|
H00118 | Congenital disorders of glycosylation (CDG) type I |
P34949
(related)
|
H00017 | Esophageal cancer |
P35354
(related)
|
H00025 | Penile cancer |
P35354
(related)
|
H00046 | Cholangiocarcinoma |
P35354
(related)
|
H00003 | Acute myeloid leukemia (AML) |
P36888
(related)
Q01196 (related) Q01196 (marker) Q13951 (marker) |
H00192 | Xanthinuria |
P47989
(related)
|
H00088 | Common variable immunodeficiency (CVID) |
P60033
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|