1,1-Ethanediol, 1,1-diacetate

Details

Top
Internal ID 8cfb4e6b-1600-4d10-b920-f401b4616cdb
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters > Acylals
IUPAC Name 1-acetyloxyethyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H10O4/c1-4(7)9-6(3)10-5(2)8/h6H,1-3H3
InChI Key ACKALUBLCWJVNB-UHFFFAOYSA-N
Popularity 173 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H10O4
Molecular Weight 146.14 g/mol
Exact Mass 146.05790880 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.46
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
RefChem:410330
ETHYLIDENE DIACETATE
542-10-9
1,1-Ethanediol Diacetate
ethane-1,1-diyl diacetate
1,1-Diacetoxyethane
Ethylidene acetate
1,1-Ethanediol, diacetate
1-acetyloxyethyl acetate
MFCD00014980
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 1,1-Ethanediol, 1,1-diacetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9614 96.14%
Caco-2 - 0.5709 57.09%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7531 75.31%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.9700 97.00%
OATP1B3 inhibitior + 0.9660 96.60%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9524 95.24%
P-glycoprotein inhibitior - 0.9643 96.43%
P-glycoprotein substrate - 0.9898 98.98%
CYP3A4 substrate - 0.7335 73.35%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8836 88.36%
CYP3A4 inhibition - 0.9241 92.41%
CYP2C9 inhibition - 0.9566 95.66%
CYP2C19 inhibition - 0.9715 97.15%
CYP2D6 inhibition - 0.9590 95.90%
CYP1A2 inhibition - 0.9546 95.46%
CYP2C8 inhibition - 0.9970 99.70%
CYP inhibitory promiscuity - 0.9525 95.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6508 65.08%
Carcinogenicity (trinary) Non-required 0.6904 69.04%
Eye corrosion + 0.9851 98.51%
Eye irritation + 0.9856 98.56%
Skin irritation - 0.5266 52.66%
Skin corrosion + 0.9425 94.25%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8792 87.92%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.6407 64.07%
skin sensitisation - 0.6467 64.67%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.7318 73.18%
Acute Oral Toxicity (c) III 0.7552 75.52%
Estrogen receptor binding - 0.8784 87.84%
Androgen receptor binding - 0.8513 85.13%
Thyroid receptor binding - 0.8957 89.57%
Glucocorticoid receptor binding - 0.9226 92.26%
Aromatase binding - 0.7590 75.90%
PPAR gamma - 0.9680 96.80%
Honey bee toxicity - 0.8415 84.15%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8355 83.55%
Fish aquatic toxicity + 0.8086 80.86%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.28% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.73% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.34% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.94% 85.14%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.09% 97.21%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Curcuma kwangsiensis
Curcuma phaeocaulis
Curcuma wenyujin
Curcuma zedoaria

Cross-Links

Top
PubChem 222536
NPASS NPC312003