| 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 |
|
|
|
C00031075
|
Ponicidin
|
CHEMBL401207
|
C090365
|
No. 83 |
|
|||
|
C00031959
|
Lasiodonin
|
No. 83 |
|
|||||
|
C00031121
|
Rabdosin B
/ (+)-Rabdosin B |
C037018
|
No. 241 | No. 41 |
|
|||
|
C00003443
|
Isodonal
|
CHEMBL453800
|
No. 241 | No. 41 |
|
|||
|
C00031769
|
Epinodosin
|
CHEMBL510160
CHEMBL1081333 |
No. 241 | No. 41 |
|
|||
|
C00031897
|
Isodonoiol
/ Rabdosin C / Rabdophyllin G |
CHEMBL452862
|
C037511
|
No. 241 | No. 41 |
|
||
|
C00031989
|
Lushanrubescensin H
/ (+)-Lushanrubescensin H |
No. 241 | No. 41 |
|
||||
|
C00031761
|
Enmenol
|
CHEMBL1080423
|
C038064
|
No. 339 |
|
|||
|
C00031885
|
Inflexusin
/ (-)-Inflexusin |
No. 481 |
|
|||||
|
C00031988
|
Lushanrubescensin G
/ (-)-Lushanrubescensin G |
No. 735 |
|
|||||
|
C00031987
|
Lushanrubescensin F
/ (-)-Lushanrubescensin F |
No. 735 |
|
|||||
|
C00031990
|
Lushanrubescensin I
/ (+)-Lushanrubescensin I |
No. 3021 |
|
| 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)
|