id | C00033820 |
---|---|
Name | Epiloganic acid |
CAS RN | 82509-41-9 |
Standard InChI | InChI=1S/C16H24O10/c1-5-8(18)2-6-7(14(22)23)4-24-15(10(5)6)26-16-13(21)12(20)11(19)9(3-17)25-16/h4-6,8-13,15-21H,2-3H2,1H3,(H,22,23)/t5-,6-,8+,9-,10-,11-,12+,13-,15+,16+/m1/s1 |
Standard InChI (Main Layer) | InChI=1S/C16H24O10/c1-5-8(18)2-6-7(14(22)23)4-24-15(10(5)6)26-16-13(21)12(20)11(19)9(3-17)25-16/h4-6,8-13,15-21H,2-3H2,1H3,(H,22,23) |
Phytochemical cluster | No. 36 |
---|---|
KCF-S cluster | No. 64 |
By standard InChI | CHEMBL1079678 |
---|---|
By standard InChI Main Layer | CHEMBL1081585 CHEMBL1079678 CHEMBL1356464 CHEMBL1452775 |
By LinkDB |
---|
By CAS RN |
---|
class name | count |
---|---|
asterids | 1 |
family name | count |
---|
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Triaenophora rupestris | 441503 | asterids | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P60033 | CD81 antigen | Unclassified protein | CHEMBL1081585 |
CHEMBL1099753
(1)
|
1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | CHEMBL1356464 |
CHEMBL1794584
(1)
|
2 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | CHEMBL1452775 |
CHEMBL1614250
(1)
CHEMBL1614421
(1)
CHEMBL1614502 (1) |
4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | CHEMBL1356464 |
CHEMBL1738184
(1)
|
0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | CHEMBL1356464 |
CHEMBL2354311
(1)
|
1 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | CHEMBL1356464 |
CHEMBL2114913
(1)
|
0 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#114500 | Colorectal cancer; crc |
P84022
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#613496 | Immunodeficiency, common variable, 6; cvid6 |
P60033
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | disease name | UniProt |
---|---|---|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00088 | Common variable immunodeficiency (CVID) |
P60033
(related)
|