PCIDB

KNApSAcK Metabolite C00001916

Metabolite

KNApSAcK Entry

id C00001916
Name Salutaridine / (+)-Salutaridine
CAS RN 1936-18-1
Standard InChI InChI=1S/C19H21NO4/c1-20-7-6-19-10-16(24-3)14(21)9-12(19)13(20)8-11-4-5-15(23-2)18(22)17(11)19/h4-5,9-10,13,22H,6-8H2,1-3H3/t13-,19+/m1/s1
Standard InChI (Main Layer) InChI=1S/C19H21NO4/c1-20-7-6-19-10-16(24-3)14(21)9-12(19)13(20)8-11-4-5-15(23-2)18(22)17(11)19/h4-5,9-10,13,22H,6-8H2,1-3H3

Cluster

Phytochemical cluster No. 4
KCF-S cluster No. 426

Link

ChEMBL

By standard InChI CHEMBL404097
By standard InChI Main Layer CHEMBL402782 CHEMBL404097

KEGG

By LinkDB C05179

CTD

By CAS RN C009270

Human Protein / Gene in interaction

3 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P24941 Cyclin-dependent kinase 2 Cdc2 CHEMBL404097 CHEMBL1067148 (1)
0 / 0
P00734 Prothrombin S1A CHEMBL402782 CHEMBL944432 (1)
4 / 2
P35372 Mu-type opioid receptor Opioid receptor CHEMBL404097 CHEMBL925793 (1) CHEMBL925795 (1)
CHEMBL925796 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (4)

OMIM preferred title UniProt
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734

KEGG DISEASE (2)

KEGG disease name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)