Metabolite

KNApSAcK Entry

id C00038095
Name (2R)-8-Methylsocotrin-4'-ol
CAS RN 956103-75-6
Standard InChI InChI=1S/C32H32O6/c1-19-31(36)28(17-23-9-16-29(38-32(19)23)21-5-12-25(34)13-6-21)27(20-3-10-24(33)11-4-20)15-8-22-7-14-26(35)18-30(22)37-2/h3-7,10-14,17-18,27,29,33-36H,8-9,15-16H2,1-2H3/t27?,29-/m1/s1
Standard InChI (Main Layer) InChI=1S/C32H32O6/c1-19-31(36)28(17-23-9-16-29(38-32(19)23)21-5-12-25(34)13-6-21)27(20-3-10-24(33)11-4-20)15-8-22-7-14-26(35)18-30(22)37-2/h3-7,10-14,17-18,27,29,33-36H,8-9,15-16H2,1-2H3

Cluster

Phytochemical cluster
KCF-S cluster No. 435

Link

ChEMBL

By standard InChI CHEMBL254647
By standard InChI Main Layer CHEMBL254647

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count
Liliopsida 1

Family

family name count
Asparagaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Dracaena cochinchinensis 593754 Asparagaceae Liliopsida Viridiplantae

Human Protein / Gene in interaction

2 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P27487 Dipeptidyl peptidase 4 S9B CHEMBL254647 CHEMBL925662 (1)
0 / 1
P00734 Prothrombin S1A CHEMBL254647 CHEMBL925661 (1)
4 / 2

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 (3)

KEGG disease name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00032 Thyroid cancer P27487 (marker)