Metabolite

KNApSAcK Entry

id C00045037
Name Puupehenone / (+)-Puupehenone
CAS RN 73573-17-8
Standard InChI InChI=1S/C21H28O3/c1-19(2)7-5-8-20(3)17(19)6-9-21(4)18(20)11-13-10-14(22)15(23)12-16(13)24-21/h10-12,17-18,22H,5-9H2,1-4H3/t17-,18+,20-,21-/m0/s1
Standard InChI (Main Layer) InChI=1S/C21H28O3/c1-19(2)7-5-8-20(3)17(19)6-9-21(4)18(20)11-13-10-14(22)15(23)12-16(13)24-21/h10-12,17-18,22H,5-9H2,1-4H3

Cluster

Phytochemical cluster
KCF-S cluster No. 3187

Link

ChEMBL

By standard InChI CHEMBL157844
By standard InChI Main Layer CHEMBL157844

KEGG

By LinkDB

CTD

By CAS RN C053594

Species

Summary

Plant class

class name count

Family

family name count

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Hyrtios sp.

Human Protein / Gene in interaction

6 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P09917 Arachidonate 5-lipoxygenase Oxidoreductase CHEMBL157844 CHEMBL1167023 (1)
0 / 0
P11597 Cholesteryl ester transfer protein Secreted protein CHEMBL157844 CHEMBL653305 (1)
1 / 1
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor CHEMBL157844 CHEMBL2185737 (1) CHEMBL2188882 (1)
CHEMBL2188884 (1) CHEMBL2188900 (1)
0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme CHEMBL157844 CHEMBL986635 (1) CHEMBL1167021 (1)
2 / 0
Q99814 Endothelial PAS domain-containing protein 1 Unclassified protein CHEMBL157844 CHEMBL2188900 (1) CHEMBL2188901 (1)
CHEMBL2188904 (1) CHEMBL2188906 (1)
CHEMBL2182284 (1) CHEMBL2182285 (1)
CHEMBL2182286 (1) CHEMBL2182287 (1)
CHEMBL2184390 (1)
1 / 1
P16050 Arachidonate 15-lipoxygenase Enzyme CHEMBL157844 CHEMBL986634 (1) CHEMBL1167022 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (4)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P18054
#611783 Erythrocytosis, familial, 4; ecyt4 Q99814
#133239 Esophageal cancer P18054
#143470 Hyperalphalipoproteinemia 1; halp1 P11597

KEGG DISEASE (2)

KEGG disease name UniProt
H01199 Hyperalphalipoproteinemia P11597 (related)
H00236 Congenital polycythemia Q99814 (related)