PCIDB

KNApSAcK Metabolite C00032520

Metabolite

KNApSAcK Entry

id C00032520
Name Xanthoxyletin
CAS RN 84-99-1
Standard InChI InChI=1S/C15H14O4/c1-15(2)7-6-10-12(19-15)8-11-9(14(10)17-3)4-5-13(16)18-11/h4-8H,1-3H3
Standard InChI (Main Layer) InChI=1S/C15H14O4/c1-15(2)7-6-10-12(19-15)8-11-9(14(10)17-3)4-5-13(16)18-11/h4-8H,1-3H3

Cluster

Phytochemical cluster No. 25
KCF-S cluster No. 750

Link

ChEMBL

By standard InChI CHEMBL501358
By standard InChI Main Layer CHEMBL501358

KEGG

By LinkDB

CTD

By CAS RN

Human Protein / Gene in interaction

14 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P43166 Carbonic anhydrase 7 Lyase CHEMBL501358 CHEMBL2341285 (1)
0 / 0
Q8N1Q1 Carbonic anhydrase 13 Lyase CHEMBL501358 CHEMBL2341282 (1)
0 / 0
P00918 Carbonic anhydrase 2 Lyase CHEMBL501358 CHEMBL2341286 (1)
1 / 2
P17405 Sphingomyelin phosphodiesterase Enzyme CHEMBL501358 CHEMBL1794495 (1)
2 / 2
O43570 Carbonic anhydrase 12 Lyase CHEMBL501358 CHEMBL2341283 (1)
1 / 2
P00915 Carbonic anhydrase 1 Lyase CHEMBL501358 CHEMBL2341287 (1)
0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor CHEMBL501358 CHEMBL2114788 (1) CHEMBL2114931 (1)
0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL501358 CHEMBL1794401 (1)
0 / 0
Q16790 Carbonic anhydrase 9 Lyase CHEMBL501358 CHEMBL2341284 (1)
0 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein CHEMBL501358 CHEMBL1738588 (1)
0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein CHEMBL501358 CHEMBL1738184 (1)
0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme CHEMBL501358 CHEMBL1613914 (1)
0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme CHEMBL501358 CHEMBL1738442 (1)
0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein CHEMBL501358 CHEMBL2354287 (1)
1 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#143860 Hyperchlorhidrosis, isolated O43570
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918

KEGG DISEASE (7)

KEGG disease name UniProt
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)