KNApSAcK Metabolite C00017739
Metabolite
KNApSAcK Entry
| id | C00017739 |
|---|---|
| Name | 1-epi-Valiolamine |
| CAS RN | 141042-85-5 |
| Standard InChI | InChI=1S/C7H15NO5/c8-3-1-7(13,2-9)6(12)5(11)4(3)10/h3-6,9-13H,1-2,8H2/t3-,4+,5-,6+,7+/m1/s1 |
| Standard InChI (Main Layer) | InChI=1S/C7H15NO5/c8-3-1-7(13,2-9)6(12)5(11)4(3)10/h3-6,9-13H,1-2,8H2 |
Cluster
| Phytochemical cluster | |
|---|---|
| KCF-S cluster | No. 4033 |
Link
ChEMBL
| By standard InChI | CHEMBL223096 |
|---|---|
| By standard InChI Main Layer | CHEMBL9216 CHEMBL223096 CHEMBL222396 |
KEGG
| By LinkDB |
|---|
CTD
| By CAS RN |
|---|
Species
Summary
Plant class
| class name | count |
|---|
Family
| family name | count |
|---|---|
| Streptomycetaceae | 1 |
List (1)
* NCBI
| KNApSAcK organism | *ID | *family | *plant class | *kingdom |
|---|---|---|---|---|
| Streptomyces hygroscopicus subsp. limoneus (IFO 12703, ATCC 21431, FERM-P 468) | 1883 | Streptomycetaceae | Bacteria |
Human Protein / Gene in interaction
4 ChEMBL Protein in interactions
| accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|---|
| P04062 | Glucosylceramidase | Enzyme | CHEMBL222396 |
CHEMBL993570
(1)
|
6 / 4 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | CHEMBL222396 |
CHEMBL993567
(1)
|
1 / 1 |
| P14410 | Sucrase-isomaltase, intestinal | Enzyme | CHEMBL9216 |
CHEMBL808823
(1)
|
1 / 1 |
| O43451 | Maltase-glucoamylase, intestinal | Hydrolase | CHEMBL9216 |
CHEMBL710105
(1)
|
0 / 0 |
Related Disease
Diseases related to proteins in ChEMBL interactions
OMIM (8)
| OMIM | preferred title | UniProt |
|---|---|---|
| #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
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| #222900 | Sucrase-isomaltase deficiency, congenital; csid |
P14410
|
KEGG DISEASE (6)
| 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)
|
| H00115 | Congenital sucrase-isomaltase deficiency |
P14410
(related)
|