PCIDB

KNApSAcK Metabolite C00030483

Index

Metabolite

Species

Human Protein
/ Gene in interactions

Related Diseases

Metabolite

KNApSAcK Entry

id	C00030483
Name	Hippuric acid
CAS RN	495-69-2
Standard InChI	InChI=1S/C9H9NO3/c11-8(12)6-10-9(13)7-4-2-1-3-5-7/h1-5H,6H2,(H,10,13)(H,11,12)
Standard InChI (Main Layer)	InChI=1S/C9H9NO3/c11-8(12)6-10-9(13)7-4-2-1-3-5-7/h1-5H,6H2,(H,10,13)(H,11,12)

Cluster

Phytochemical cluster
KCF-S cluster	No. 7440

Link

ChEMBL

By standard InChI	CHEMBL461
By standard InChI Main Layer	CHEMBL461

KEGG

By LinkDB	C01586

CTD

By CAS RN	C030514

Species

Summary

Plant class

class name	count
Magnoliophyta	1

Family

family name	count
Lauraceae	1

List (1)

* NCBI

KNApSAcK organism	*ID	*family	*plant class	*kingdom
Persea americana	3435	Lauraceae	Magnoliophyta	Viridiplantae

Human Protein / Gene in interaction

8 ChEMBL Protein in interactions

accession	description	class description	compound	assay ID (# of activities)	# of diseases (OMIM / KEGG)
Q16719	Kynureninase	Enzyme	CHEMBL461	CHEMBL1009939 (1)	0 / 0
P02545	Prelamin-A/C	Unclassified protein	CHEMBL461	CHEMBL1614544 (1)	11 / 10
P08183	Multidrug resistance protein 1	drug	CHEMBL461	CHEMBL2077528 (1)	1 / 0
P84022	Mothers against decapentaplegic homolog 3	Unclassified protein	CHEMBL461	CHEMBL1794584 (1)	2 / 0
Q8TCC7	Solute carrier family 22 member 8	Antiporter	CHEMBL461	CHEMBL2075340 (1)	0 / 0
Q4U2R8	Solute carrier family 22 member 6	Antiporter	CHEMBL461	CHEMBL1781812 (1) CHEMBL2077573 (1) CHEMBL2077511 (1) CHEMBL2077846 (1)	0 / 0
Q13951	Core-binding factor subunit beta	Unclassified protein	CHEMBL461	CHEMBL1613933 (1)	0 / 1
Q01196	Runt-related transcription factor 1	Unclassified protein	CHEMBL461	CHEMBL1613933 (1)	1 / 6

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
#610140	Heart-hand syndrome, slovenian type	P02545
#176670	Hutchinson-gilford progeria syndrome; hgps	P02545
#612244	Inflammatory bowel disease 13; ibd13	P08183
#151660	Lipodystrophy, familial partial, type 2; fpld2	P02545
#613795	Loeys-dietz syndrome, type 3; lds3	P84022
#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
#601399	Platelet disorder, familial, with associated myeloid malignancy	Q01196
#275210	Restrictive dermopathy, lethal	P02545

KEGG DISEASE (14)

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)
H00001	Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia)	Q01196 (related) Q01196 (marker)
H00003	Acute myeloid leukemia (AML)	Q01196 (related) Q01196 (marker) Q13951 (marker)
H00004	Chronic myeloid leukemia (CML)	Q01196 (related)
H00978	Thrombocytopenia (THC)	Q01196 (related)