Metabolite

KNApSAcK Entry

id C00001206
Name L-(+)-Tartaric acid
CAS RN 87-69-4
Standard InChI InChI=1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)/t1-,2-/m1/s1
Standard InChI (Main Layer) InChI=1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)

Cluster

Phytochemical cluster
KCF-S cluster No. 5453

Link

ChEMBL

By standard InChI CHEMBL1236315
By standard InChI Main Layer CHEMBL225983 CHEMBL1200861 CHEMBL1236315

KEGG

By LinkDB C00898

CTD

By CAS RN

Human Protein / Gene in interaction

11 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 CHEMBL1200861 CHEMBL1741321 (1)
1 / 0
Q99489 D-aspartate oxidase Enzyme CHEMBL225983 CHEMBL2327933 (2)
0 / 0
P16473 Thyrotropin receptor Glycohormone receptor CHEMBL1200861 CHEMBL1614281 (1) CHEMBL1614361 (1)
3 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 CHEMBL1200861 CHEMBL1741325 (1)
0 / 1
P14920 D-amino-acid oxidase Enzyme CHEMBL225983 CHEMBL2327932 (1)
0 / 0
O75496 Geminin Unclassified protein CHEMBL1200861 CHEMBL1236315 CHEMBL2114843 (2) CHEMBL2114780 (1)
0 / 0
Q9GZT4 Serine racemase Enzyme CHEMBL225983 CHEMBL2327930 (2)
0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 CHEMBL1200861 CHEMBL1741322 (1)
0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 CHEMBL1200861 CHEMBL1741323 (1)
1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 CHEMBL1200861 CHEMBL1741324 (1)
0 / 1
O75164 Lysine-specific demethylase 4A Enzyme CHEMBL1200861 CHEMBL1236315 CHEMBL1737991 (2)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473

KEGG DISEASE (5)

KEGG disease name UniProt
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)