Metabolite

KNApSAcK Entry

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

Cluster

Phytochemical cluster
KCF-S cluster No. 795

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL278373 CHEMBL468154 CHEMBL1222251 CHEMBL1231671 CHEMBL1950780

KEGG

By LinkDB C00137

CTD

By CAS RN

Species

Summary


List (25)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Arabidopsis thaliana 3702 Brassicaceae rosids Viridiplantae
Centrosema pubescens 185703 Fabaceae rosids Viridiplantae
Dalbergia sissoo 107308 Fabaceae rosids Viridiplantae
Desmodium intortum 556506 Fabaceae rosids Viridiplantae
Desmodium uncinatum 225101 Fabaceae rosids Viridiplantae
Lablab purpureus 35936 Fabaceae rosids Viridiplantae
Lens culinaris 3864 Fabaceae rosids Viridiplantae
Liriodendron tulipifera 3415 Magnoliaceae Magnoliophyta Viridiplantae
Lotononis angolensis 76394 Fabaceae rosids Viridiplantae
Lotononis bainesii 228755 Fabaceae rosids Viridiplantae
Macroptilium atropurpureum 90550 Fabaceae rosids Viridiplantae
Macroptilium bracteatum 260883 Fabaceae rosids Viridiplantae
Macroptilium lathyroides 260885 Fabaceae rosids Viridiplantae
Macrotyloma axillare 3876 Fabaceae rosids Viridiplantae
Macrotyloma uniflorum 271171 Fabaceae rosids Viridiplantae
Marsdenia tomentosa 276779 Apocynaceae asterids Viridiplantae
Medicago sativa 3879 Fabaceae rosids Viridiplantae
Phaseolus vulgaris 3885 Fabaceae rosids Viridiplantae
Pueraria phaseoloides 109224 Fabaceae rosids Viridiplantae
Rhynchosia beddomei 1378005 Fabaceae rosids Viridiplantae
Rhynchosia hirta 132460 Fabaceae rosids Viridiplantae
Sebertia acuminata 280718 Sapotaceae asterids Viridiplantae
Solanum lycopersicum L. 4081 Solanaceae asterids Viridiplantae
Stylosanthes guianensis 62615 Fabaceae rosids Viridiplantae
Stylosanthes humilis 35628 Fabaceae rosids Viridiplantae

Human Protein / Gene in interaction

8 ChEMBL Protein in interactions

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

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (17)

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 (18)

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)