PCIDB

KNApSAcK Metabolite C00037426

Metabolite

KNApSAcK Entry

id C00037426
Name L-Mandelic acid / L-(+)-Mandelic acid
CAS RN 17199-29-0
Standard InChI InChI=1S/C8H8O3/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7,9H,(H,10,11)/t7-/m0/s1
Standard InChI (Main Layer) InChI=1S/C8H8O3/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7,9H,(H,10,11)

Cluster

Phytochemical cluster
KCF-S cluster No. 2481

Link

ChEMBL

By standard InChI CHEMBL58910
By standard InChI Main Layer CHEMBL58910 CHEMBL292411 CHEMBL1609

KEGG

By LinkDB C01984

CTD

By CAS RN

Species

Summary

Plant class

class name count
asterids 1

Family

family name count
Adoxaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Sambucus nigra 4202 Adoxaceae asterids Viridiplantae

Human Protein / Gene in interaction

12 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr CHEMBL58910 CHEMBL292411 CHEMBL770117 (2)
0 / 0
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme CHEMBL58910 CHEMBL292411 CHEMBL1609 CHEMBL1614063 (3)
0 / 0
P02545 Prelamin-A/C Unclassified protein CHEMBL1609 CHEMBL1614544 (1)
11 / 10
P14902 Indoleamine 2,3-dioxygenase 1 Enzyme CHEMBL1609 CHEMBL2092115 (1)
0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein CHEMBL58910 CHEMBL1794584 (1)
2 / 0
P08107 Heat shock 70 kDa protein 1A/1B Unclassified protein CHEMBL1609 CHEMBL1614297 (1)
0 / 0
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr CHEMBL58910 CHEMBL292411 CHEMBL1609 CHEMBL1613806 (3)
0 / 0
P98170 E3 ubiquitin-protein ligase XIAP Other cytosolic protein CHEMBL58910 CHEMBL1614251 (1) CHEMBL1614228 (1)
1 / 1
O75164 Lysine-specific demethylase 4A Enzyme CHEMBL1609 CHEMBL1737991 (1)
0 / 0
Q9UBT6 DNA polymerase kappa Enzyme CHEMBL1609 CHEMBL1794536 (2)
0 / 0
P11142 Heat shock cognate 71 kDa protein Unclassified protein CHEMBL1609 CHEMBL1614143 (1)
0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme CHEMBL58910 CHEMBL2354311 (1)
1 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (15)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#137800 Glioma susceptibility 1; glm1 O75874
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#300635 Lymphoproliferative syndrome, x-linked, 2; xlp2 P98170
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#275210 Restrictive dermopathy, lethal P02545

KEGG DISEASE (11)

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)
H00107 Other well-defined immunodeficiency syndromes P98170 (related)