Metabolite

KNApSAcK Entry

id C00018229
Name Tetrahydrobiopterin
CAS RN 17528-72-2
Standard InChI InChI=1S/C9H15N5O3/c1-3(15)6(16)4-2-11-7-5(12-4)8(17)14-9(10)13-7/h3-4,6,12,15-16H,2H2,1H3,(H4,10,11,13,14,17)
Standard InChI (Main Layer) InChI=1S/C9H15N5O3/c1-3(15)6(16)4-2-11-7-5(12-4)8(17)14-9(10)13-7/h3-4,6,12,15-16H,2H2,1H3,(H4,10,11,13,14,17)

Cluster

Phytochemical cluster
KCF-S cluster No. 7555

Link

ChEMBL

By standard InChI CHEMBL337765
By standard InChI Main Layer CHEMBL337765 CHEMBL270788 CHEMBL1201774 CHEMBL1315516 CHEMBL1616454

KEGG

By LinkDB C00272

CTD

By CAS RN C003402

Species

Summary

Plant class

class name count

Family

family name count
Enterobacteriaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Escherichia coli 562 Enterobacteriaceae Bacteria

Human Protein / Gene in interaction

14 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P29475 Nitric oxide synthase, brain Enzyme CHEMBL1201774 CHEMBL934143 (2)
0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 CHEMBL1315516 CHEMBL1741321 (1)
1 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein CHEMBL270788 CHEMBL1794499 (1)
2 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme CHEMBL1315516 CHEMBL1614331 (1)
0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 CHEMBL1315516 CHEMBL1741325 (1)
0 / 1
Q92830 Histone acetyltransferase KAT2A Enzyme CHEMBL270788 CHEMBL1738606 (1)
0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme CHEMBL270788 CHEMBL1794467 (1)
0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 CHEMBL1315516 CHEMBL1741322 (1)
0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme CHEMBL1315516 CHEMBL1613910 (1) CHEMBL1614227 (1)
3 / 3
P55210 Caspase-7 C14 CHEMBL1315516 CHEMBL1613779 (1)
0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 CHEMBL1315516 CHEMBL1741323 (1)
1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 CHEMBL1315516 CHEMBL1741324 (1)
0 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein CHEMBL270788 CHEMBL1737980 (1)
0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme CHEMBL270788 CHEMBL1738442 (2)
0 / 0

CTD interaction (4)

compound gene gene name gene description interaction interaction type form reference
pmid
C003402 2643 GCH1
DYT14
DYT5
DYT5a
GCH
GTP-CH-1
GTPCH1
HPABH4B
GTP cyclohydrolase 1 (EC:3.5.4.16) GCH1 protein results in increased chemical synthesis of 5,6,7,8-tetrahydrobiopterin increases chemical synthesis
protein 14551046
C003402 4846 NOS3
ECNOS
eNOS
nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) 5,6,7,8-tetrahydrobiopterin deficiency inhibits the reaction [NOS3 protein results in increased abundance of Superoxides] decreases reaction
/ increases abundance
protein 19011239
C003402 4846 NOS3
ECNOS
eNOS
nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) 5,6,7,8-tetrahydrobiopterin deficiency promotes the reaction [NOS3 protein results in increased abundance of Superoxides] increases abundance
/ increases reaction
protein 19011239
C003402 6343 SCT
secretin SCT protein results in increased abundance of 5,6,7,8-tetrahydrobiopterin increases abundance
protein 16168596

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798

KEGG DISEASE (6)

KEGG disease name UniProt
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)

Diseases related to CTD interactions

5 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D001321 C003402 Autistic Disorder therapeutic
16160627
D001927 C003402 Brain Diseases marker/mechanism
1389541
D002318 C003402 Cardiovascular Diseases marker/mechanism
20610621
D064420 C003402 Drug-Related Side Effects and Adverse Reactions marker/mechanism
1389541
D024821 C003402 Metabolic Syndrome X therapeutic
17098227