PCIDB

KNApSAcK Metabolite C00034882

Metabolite

KNApSAcK Entry

id C00034882
Name Nonane / n-Nonane
CAS RN 111-84-2
Standard InChI InChI=1S/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H3
Standard InChI (Main Layer) InChI=1S/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H3

Cluster

Phytochemical cluster
KCF-S cluster No. 1749

Link

ChEMBL

By standard InChI CHEMBL335900
By standard InChI Main Layer CHEMBL335900

KEGG

By LinkDB

CTD

By CAS RN C017573

Species

Summary

Plant class

class name count
asterids 1

Family

family name count
Solanaceae 1
Ganodermataceae 1

List (2)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Ganoderma lucidum 5315 Ganodermataceae Fungi
Lycopersicon esculentum Mill. 4081 Solanaceae asterids Viridiplantae

Human Protein / Gene in interaction

1 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P16473 Thyrotropin receptor Glycohormone receptor CHEMBL335900 CHEMBL1614281 (1) CHEMBL1614361 (1)
3 / 2

CTD interaction (4)

compound gene gene name gene description interaction interaction type form reference
pmid
C017573 3569 IL6
BSF2
HGF
HSF
IFNB2
IL-6
interleukin 6 (interferon, beta 2) nonane results in increased expression of and results in increased secretion of IL6 protein increases expression
/ increases secretion
protein 19720135
C017573 3576 IL8
CXCL8
GCP-1
GCP1
LECT
LUCT
LYNAP
MDNCF
MONAP
NAF
NAP-1
NAP1
interleukin 8 nonane results in increased secretion of IL8 protein increases secretion
protein 19720135
C017573 5241 PGR
NR3C3
PR
progesterone receptor nonane results in increased expression of PGR mRNA alternative form increases expression
mRNA 16009159
C017573 5241 PGR
NR3C3
PR
progesterone receptor nonane results in increased expression of PGR protein alternative form increases expression
protein 16009159

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (3)

OMIM preferred title UniProt
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473

KEGG DISEASE (2)

KEGG disease name UniProt
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)

Diseases related to CTD interactions

2 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D017453 C017573 Dermatitis, Irritant marker/mechanism
19152832
D004890 C017573 Erythema marker/mechanism
15451557
19720135