| id | C00001810 |
|---|---|
| Name | Armepavine / (-)-Armepavine / (R)-(-)-Armepavine |
| CAS RN | 524-20-9 |
| Standard InChI | InChI=1S/C19H23NO3/c1-20-9-8-14-11-18(22-2)19(23-3)12-16(14)17(20)10-13-4-6-15(21)7-5-13/h4-7,11-12,17,21H,8-10H2,1-3H3/t17-/m1/s1 |
| Standard InChI (Main Layer) | InChI=1S/C19H23NO3/c1-20-9-8-14-11-18(22-2)19(23-3)12-16(14)17(20)10-13-4-6-15(21)7-5-13/h4-7,11-12,17,21H,8-10H2,1-3H3 |
| Phytochemical cluster | No. 4 |
|---|---|
| KCF-S cluster | No. 345 |
| By standard InChI | CHEMBL1186510 |
|---|---|
| By standard InChI Main Layer | CHEMBL451722 CHEMBL1186477 CHEMBL1186510 |
| By LinkDB | C09342 |
|---|
| By CAS RN |
|---|
| class name | count |
|---|---|
| eudicotyledons | 7 |
| rosids | 3 |
| Magnoliophyta | 2 |
| family name | count |
|---|---|
| Papaveraceae | 4 |
| Celastraceae | 2 |
| Berberidaceae | 2 |
| Lauraceae | 2 |
| Nelumbonaceae | 1 |
| Rhamnaceae | 1 |
| accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|---|
| P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL451722 |
CHEMBL1614458
(1)
|
0 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | CHEMBL451722 |
CHEMBL1794584
(1)
|
2 / 0 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | CHEMBL451722 |
CHEMBL1614227
(1)
|
3 / 3 |
| P16050 | Arachidonate 15-lipoxygenase | Enzyme | CHEMBL451722 |
CHEMBL1614240
(1)
|
0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL451722 |
CHEMBL1613914
(1)
|
0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | CHEMBL451722 |
CHEMBL1738442
(1)
|
0 / 0 |
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | CHEMBL451722 |
CHEMBL2114738
(1)
|
0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|