Organism name | Isodon rubescens var. lushanensis |
---|---|
Genus | Isodon |
Family | Labiatae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Isodon |
---|---|
Linked NCBI taxonomy ID | 204130 |
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 |
---|---|---|---|---|---|---|---|---|
C00001078
![]() |
Lutexin
/ Orientin / Luteolin 8-C-beta-D-glucopyranoside / 8-beta-D-Glucopyranosyl-3',4',5,7-tetrahydroxyflavone |
CHEMBL520866
CHEMBL1468796 |
C065886
|
20 / 15 / 14 | No. 22 | No. 15 |
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|
C00031075
![]() |
Ponicidin
|
CHEMBL401207
|
C090365
|
No. 83 |
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|||
C00031959
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Lasiodonin
|
No. 83 |
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|||||
C00031121
![]() |
Rabdosin B
/ (+)-Rabdosin B |
C037018
|
No. 241 | No. 41 |
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|||
C00003443
![]() |
Isodonal
|
CHEMBL453800
|
No. 241 | No. 41 |
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|||
C00031769
![]() |
Epinodosin
|
CHEMBL510160
CHEMBL1081333 |
No. 241 | No. 41 |
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|||
C00031897
![]() |
Isodonoiol
/ Rabdosin C / Rabdophyllin G |
CHEMBL452862
|
C037511
|
No. 241 | No. 41 |
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||
C00031989
![]() |
Lushanrubescensin H
/ (+)-Lushanrubescensin H |
No. 241 | No. 41 |
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||||
C00031761
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Enmenol
|
CHEMBL1080423
|
C038064
|
No. 339 |
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|||
C00031885
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Inflexusin
/ (-)-Inflexusin |
No. 481 |
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|||||
C00031988
![]() |
Lushanrubescensin G
/ (-)-Lushanrubescensin G |
No. 735 |
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|||||
C00031987
![]() |
Lushanrubescensin F
/ (-)-Lushanrubescensin F |
No. 735 |
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|||||
C00031990
![]() |
Lushanrubescensin I
/ (+)-Lushanrubescensin I |
No. 3021 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00001078 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00001078 | 1 / 1 |
P06746 | DNA polymerase beta | Enzyme | C00001078 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00001078 | 1 / 1 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00001078 | 0 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00001078 | 3 / 1 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00001078 | 1 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00001078 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00001078 | 1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00001078 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00001078 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00001078 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00001078 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00001078 | 4 / 3 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00001078 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001078 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00001078 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00001078 | 1 / 1 |
O00255 | Menin | Unclassified protein | C00001078 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00001078 | 1 / 2 |
OMIM | preferred title | UniProt |
---|---|---|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#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
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
|
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
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)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|