3,3-Diethoxy-1-propanol

Details

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Internal ID 73b9395f-e3c4-45f5-9005-84e544aa7c77
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals
IUPAC Name 3,3-diethoxypropan-1-ol
SMILES (Canonical) CCOC(CCO)OCC
SMILES (Isomeric) CCOC(CCO)OCC
InChI InChI=1S/C7H16O3/c1-3-9-7(5-6-8)10-4-2/h7-8H,3-6H2,1-2H3
InChI Key ASERXEZXVIJBRO-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C7H16O3
Molecular Weight 148.20 g/mol
Exact Mass 148.109944368 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.77
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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16777-87-0
3,3-diethoxypropan-1-ol
3,3-diethoxypropanol
1-Propanol, 3,3-diethoxy-
MFCD00074850
3-hydroxypropionaldehyde diethyl acetal
3, 3-diethoxypropanol
SCHEMBL440376
DTXSID30168369
3,3-Diethoxy-1-propanol, 98%
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,3-Diethoxy-1-propanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9747 97.47%
Caco-2 + 0.7245 72.45%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5815 58.15%
OATP2B1 inhibitior - 0.8391 83.91%
OATP1B1 inhibitior + 0.9383 93.83%
OATP1B3 inhibitior + 0.9411 94.11%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9100 91.00%
P-glycoprotein inhibitior - 0.9724 97.24%
P-glycoprotein substrate - 0.9584 95.84%
CYP3A4 substrate - 0.6953 69.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7881 78.81%
CYP3A4 inhibition - 0.8959 89.59%
CYP2C9 inhibition - 0.9434 94.34%
CYP2C19 inhibition - 0.9144 91.44%
CYP2D6 inhibition - 0.9317 93.17%
CYP1A2 inhibition - 0.8799 87.99%
CYP2C8 inhibition - 0.9892 98.92%
CYP inhibitory promiscuity - 0.9063 90.63%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.6919 69.19%
Eye corrosion + 0.8395 83.95%
Eye irritation + 0.9911 99.11%
Skin irritation - 0.7497 74.97%
Skin corrosion - 0.9707 97.07%
Ames mutagenesis - 0.8007 80.07%
Human Ether-a-go-go-Related Gene inhibition - 0.6168 61.68%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5871 58.71%
skin sensitisation - 0.8053 80.53%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.7104 71.04%
Acute Oral Toxicity (c) III 0.6260 62.60%
Estrogen receptor binding - 0.9070 90.70%
Androgen receptor binding - 0.9108 91.08%
Thyroid receptor binding - 0.7873 78.73%
Glucocorticoid receptor binding - 0.8327 83.27%
Aromatase binding - 0.8883 88.83%
PPAR gamma - 0.8879 88.79%
Honey bee toxicity - 0.9260 92.60%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.9700 97.00%
Fish aquatic toxicity - 0.6656 66.56%

Targets

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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 93.48% 96.09%
CHEMBL4072 P07858 Cathepsin B 84.78% 93.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.19% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.73% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.10% 96.95%

Plants that contains it

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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.
Paris polyphylla

Cross-Links

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PubChem 140135
NPASS NPC151059