| id | C00001164 |
|---|---|
| Name | Myoinositol / myo-Inositol |
| CAS RN | 87-89-8 |
| Standard InChI | InChI=1S/C6H12O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-12H/t1-,2-,3?,4?,5-,6?/m0/s1 |
| Standard InChI (Main Layer) | InChI=1S/C6H12O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-12H |
| Phytochemical cluster | |
|---|---|
| KCF-S cluster | No. 795 |
| By standard InChI | |
|---|---|
| By standard InChI Main Layer | CHEMBL278373 CHEMBL468154 CHEMBL1222251 CHEMBL1231671 CHEMBL1950780 |
| By LinkDB | C00137 |
|---|
| By CAS RN |
|---|
| class name | count |
|---|---|
| rosids | 21 |
| asterids | 3 |
| Magnoliophyta | 1 |
| family name | count |
|---|---|
| Fabaceae | 20 |
| Solanaceae | 1 |
| Apocynaceae | 1 |
| Magnoliaceae | 1 |
| Sapotaceae | 1 |
| Brassicaceae | 1 |
| accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|---|
| P10323 | Acrosin | S1A | CHEMBL1222251 |
CHEMBL639765
(1)
|
0 / 0 |
| P02545 | Prelamin-A/C | Unclassified protein | CHEMBL1222251 |
CHEMBL1614544
(1)
|
11 / 10 |
| P16278 | Beta-galactosidase | Enzyme | CHEMBL1222251 |
CHEMBL651844
(1)
|
4 / 6 |
| O75496 | Geminin | Unclassified protein | CHEMBL1231671 |
CHEMBL2114780
(1)
|
0 / 0 |
| P06280 | Alpha-galactosidase A | Enzyme | CHEMBL1222251 |
CHEMBL647608
(1)
|
1 / 1 |
| Q9UNA4 | DNA polymerase iota | Enzyme | CHEMBL278373 CHEMBL1231671 |
CHEMBL1794483
(2)
|
0 / 0 |
| O43451 | Maltase-glucoamylase, intestinal | Hydrolase | CHEMBL1222251 |
CHEMBL649327
(1)
|
0 / 0 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | CHEMBL1222251 |
CHEMBL2354287
(1)
|
1 / 1 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #301500 | Fabry disease |
P06280
|
| #230500 | Gm1-gangliosidosis, type i |
P16278
|
| #230600 | Gm1-gangliosidosis, type ii |
P16278
|
| #230650 | Gm1-gangliosidosis, type iii |
P16278
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #253010 | Mucopolysaccharidosis type ivb |
P16278
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| KEGG | disease name | UniProt |
|---|---|---|
| H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
| H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
| H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
| H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
| H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
| H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
| H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
| H00663 | Restrictive dermopathy |
P02545
(related)
|
| H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
| H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
| H00125 | Fabry disease |
P06280
(related)
|
| H00123 | Mucopolysaccharidosis type IV (MPS4) |
P16278
(related)
|
| H00276 | Galactosialidosis |
P16278
(related)
|
| H00281 | GM1 gangliosidosis |
P16278
(related)
|
| H00421 | Mucopolysaccharidosis (MPS) |
P16278
(related)
|
| H00422 | Glycoproteinoses |
P16278
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P16278
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|