id | C00006229 |
---|---|
Name | Vicenin 2 / Apigenin 6,8-di-C-glucoside |
CAS RN | 23666-13-9 |
Standard InChI | InChI=1S/C27H30O15/c28-6-12-17(32)21(36)23(38)26(41-12)15-19(34)14-10(31)5-11(8-1-3-9(30)4-2-8)40-25(14)16(20(15)35)27-24(39)22(37)18(33)13(7-29)42-27/h1-5,12-13,17-18,21-24,26-30,32-39H,6-7H2/t12?,13?,17-,18-,21+,22+,23?,24?,26+,27+/m1/s1 |
Standard InChI (Main Layer) | InChI=1S/C27H30O15/c28-6-12-17(32)21(36)23(38)26(41-12)15-19(34)14-10(31)5-11(8-1-3-9(30)4-2-8)40-25(14)16(20(15)35)27-24(39)22(37)18(33)13(7-29)42-27/h1-5,12-13,17-18,21-24,26-30,32-39H,6-7H2 |
Phytochemical cluster | No. 15 |
---|---|
KCF-S cluster | No. 1 |
By standard InChI | |
---|---|
By standard InChI Main Layer | CHEMBL1442950 |
By LinkDB | C10195 |
---|
By CAS RN |
---|
class name | count |
---|---|
asterids | 15 |
rosids | 7 |
Liliopsida | 2 |
eudicotyledons | 1 |
family name | count |
---|---|
Lamiaceae | 10 |
Asteraceae | 4 |
Fabaceae | 3 |
Violaceae | 2 |
Poaceae | 1 |
Cyperaceae | 1 |
Cucurbitaceae | 1 |
Plantaginaceae | 1 |
Caryophyllaceae | 1 |
Rutaceae | 1 |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P04062 | Glucosylceramidase | Enzyme | CHEMBL1442950 |
CHEMBL1613818
(1)
|
6 / 4 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | CHEMBL1442950 |
CHEMBL1614103
(1)
CHEMBL1614031
(1)
|
1 / 1 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | CHEMBL1442950 |
CHEMBL2114810
(1)
|
7 / 3 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | CHEMBL1442950 |
CHEMBL1614211
(1)
|
0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL1442950 |
CHEMBL1613914
(1)
|
0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | CHEMBL1442950 |
CHEMBL1738442
(1)
|
0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#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
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#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
|
KEGG | disease name | UniProt |
---|---|---|
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)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|