id | C00002451 |
---|---|
Name | Archangelicin |
CAS RN | 2607-56-9 |
Standard InChI | InChI=1S/C24H26O7/c1-7-13(3)22(26)30-20-18-16(11-9-15-10-12-17(25)29-19(15)18)28-21(20)24(5,6)31-23(27)14(4)8-2/h7-12,20-21H,1-6H3/b13-7-,14-8-/t20-,21+/m1/s1 |
Standard InChI (Main Layer) | InChI=1S/C24H26O7/c1-7-13(3)22(26)30-20-18-16(11-9-15-10-12-17(25)29-19(15)18)28-21(20)24(5,6)31-23(27)14(4)8-2/h7-12,20-21H,1-6H3 |
Phytochemical cluster | No. 25 |
---|---|
KCF-S cluster | No. 224 |
By standard InChI | CHEMBL1426896 |
---|---|
By standard InChI Main Layer | CHEMBL1426896 |
By LinkDB | C09116 |
---|
By CAS RN |
---|
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Angelica archangelica | 40949 | Apiaceae | asterids | Viridiplantae |
Angelica keiskei | 357850 | Apiaceae | asterids | Viridiplantae |
Angelica longeradiata | 40948 | Apiaceae | asterids | Viridiplantae |
Cnidium japonicum | 48111 | Apiaceae | asterids | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | CHEMBL1426896 |
CHEMBL2114784
(1)
|
1 / 1 |
P06746 | DNA polymerase beta | Enzyme | CHEMBL1426896 |
CHEMBL1614079
(1)
|
0 / 0 |
P49146 | Neuropeptide Y receptor type 2 | Neuropeptide Y receptor | CHEMBL1426896 |
CHEMBL1614345
(1)
|
0 / 0 |
P25929 | Neuropeptide Y receptor type 1 | Neuropeptide Y receptor | CHEMBL1426896 |
CHEMBL1613956
(1)
|
0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL1426896 |
CHEMBL1614458
(1)
|
0 / 0 |
P42858 | Huntingtin | Unclassified protein | CHEMBL1426896 |
CHEMBL1613918
(1)
|
1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | CHEMBL1426896 |
CHEMBL1794584
(1)
|
2 / 0 |
O75496 | Geminin | Unclassified protein | CHEMBL1426896 |
CHEMBL2114843
(1)
|
0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | CHEMBL1426896 |
CHEMBL2114788
(1)
|
0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | CHEMBL1426896 |
CHEMBL2114817
(1)
|
7 / 3 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | CHEMBL1426896 |
CHEMBL1794401
(1)
|
0 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | CHEMBL1426896 |
CHEMBL1614038
(1)
|
2 / 2 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | CHEMBL1426896 |
CHEMBL1738588
(1)
|
0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | CHEMBL1426896 |
CHEMBL1614250
(1)
|
4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | CHEMBL1426896 |
CHEMBL1738184
(1)
|
0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL1426896 |
CHEMBL1613914
(1)
|
0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | CHEMBL1426896 |
CHEMBL2354311
(1)
|
1 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#114500 | Colorectal cancer; crc |
P84022
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#143100 | Huntington disease; hd |
P42858
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | disease name | UniProt |
---|---|---|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|