id | C00001308 |
---|---|
Name | Ethyl acetate |
CAS RN | 141-78-6 |
Standard InChI | InChI=1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3 |
Standard InChI (Main Layer) | InChI=1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3 |
Phytochemical cluster | |
---|---|
KCF-S cluster | No. 4274 |
By standard InChI | CHEMBL14152 |
---|---|
By standard InChI Main Layer | CHEMBL14152 |
By LinkDB | C00849 |
---|
By CAS RN | C007650 |
---|
class name | count |
---|---|
Magnoliophyta | 2 |
rosids | 1 |
asterids | 1 |
Liliopsida | 1 |
family name | count |
---|---|
Winteraceae | 2 |
Euphorbiaceae | 1 |
Oleaceae | 1 |
Orchidaceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Croton lechleri Mull.Arg. | 100370 | Euphorbiaceae | rosids | Viridiplantae |
Dendrobium superbum | 37818 | Orchidaceae | Liliopsida | Viridiplantae |
Exospermum stipitatum | 132894 | Winteraceae | Magnoliophyta | Viridiplantae |
Olea europaea | 4146 | Oleaceae | asterids | Viridiplantae |
Zygogynum spp. | 13356 | Winteraceae | Magnoliophyta | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P02545 | Prelamin-A/C | Unclassified protein | CHEMBL14152 |
CHEMBL1614544
(1)
|
11 / 10 |
P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL14152 |
CHEMBL1614458
(1)
|
0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | CHEMBL14152 |
CHEMBL2114931
(1)
|
0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | CHEMBL14152 |
CHEMBL1613910
(1)
CHEMBL1614227
(1)
|
3 / 3 |
compound | gene | gene name | gene description | interaction | interaction type | form |
reference
pmid |
---|---|---|---|---|---|---|---|
C007650 | 6352 |
CCL5
D17S136E RANTES SCYA5 SIS-delta SISd TCP228 eoCP |
chemokine (C-C motif) ligand 5 | ethyl acetate results in increased expression of CCL5 protein |
increases expression
|
protein |
11306435
|
C007650 | 1437 |
CSF2
GMCSF |
colony stimulating factor 2 (granulocyte-macrophage) | ethyl acetate results in increased expression of CSF2 protein |
increases expression
|
protein |
11306435
|
C007650 | 4790 |
NFKB1
EBP-1 KBF1 NF-kB1 NF-kappa-B NF-kappaB NFKB-p105 NFKB-p50 NFkappaB p105 p50 |
nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 | ethyl acetate results in increased localization of and results in increased activity of NFKB1 protein |
increases activity
/ increases localization |
protein |
11306435
|
C007650 | 5970 |
RELA
NFKB3 p65 |
v-rel avian reticuloendotheliosis viral oncogene homolog A | ethyl acetate results in increased localization of and results in increased activity of RELA protein |
increases activity
/ increases localization |
protein |
11306435
|
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
KEGG | disease name | UniProt |
---|---|---|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
H00663 | Restrictive dermopathy |
P02545
(related)
|
H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|