Valeric anhydride

Details

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Internal ID 712990a4-d8f5-4c33-8656-c9470289fb76
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Dicarboxylic acids and derivatives
IUPAC Name pentanoyl pentanoate
SMILES (Canonical) CCCCC(=O)OC(=O)CCCC
SMILES (Isomeric) CCCCC(=O)OC(=O)CCCC
InChI InChI=1S/C10H18O3/c1-3-5-7-9(11)13-10(12)8-6-4-2/h3-8H2,1-2H3
InChI Key DUCKXCGALKOSJF-UHFFFAOYSA-N
Popularity 53 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O3
Molecular Weight 186.25 g/mol
Exact Mass 186.125594432 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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2082-59-9
Pentanoic anhydride
Pentanoic acid, 1,1'-anhydride
Pentanoic acid, anhydride
N9B5ZQ67R5
DTXSID70870934
EINECS 218-212-9
RefChem:901587
DTXCID70818614
218-212-9
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Valeric anhydride

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.8701 87.01%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7186 71.86%
OATP2B1 inhibitior - 0.8378 83.78%
OATP1B1 inhibitior + 0.9080 90.80%
OATP1B3 inhibitior + 0.9531 95.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8516 85.16%
P-glycoprotein inhibitior - 0.9405 94.05%
P-glycoprotein substrate - 0.9628 96.28%
CYP3A4 substrate - 0.6787 67.87%
CYP2C9 substrate - 0.6061 60.61%
CYP2D6 substrate - 0.8514 85.14%
CYP3A4 inhibition - 0.9578 95.78%
CYP2C9 inhibition - 0.8805 88.05%
CYP2C19 inhibition - 0.8826 88.26%
CYP2D6 inhibition - 0.9546 95.46%
CYP1A2 inhibition - 0.6968 69.68%
CYP2C8 inhibition - 0.9443 94.43%
CYP inhibitory promiscuity - 0.9342 93.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5623 56.23%
Carcinogenicity (trinary) Non-required 0.6573 65.73%
Eye corrosion + 0.9886 98.86%
Eye irritation + 0.9618 96.18%
Skin irritation - 0.6374 63.74%
Skin corrosion + 0.9671 96.71%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8521 85.21%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5249 52.49%
skin sensitisation - 0.8372 83.72%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity - 0.8909 89.09%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5479 54.79%
Acute Oral Toxicity (c) III 0.5481 54.81%
Estrogen receptor binding - 0.9324 93.24%
Androgen receptor binding - 0.8875 88.75%
Thyroid receptor binding - 0.8133 81.33%
Glucocorticoid receptor binding - 0.9041 90.41%
Aromatase binding - 0.9029 90.29%
PPAR gamma - 0.7125 71.25%
Honey bee toxicity - 0.9916 99.16%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5268 52.68%
Fish aquatic toxicity + 0.9367 93.67%

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 94.32% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.87% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.78% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.35% 96.95%
CHEMBL230 P35354 Cyclooxygenase-2 81.80% 89.63%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.47% 97.21%

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.
Capsella bursa-pastoris

Cross-Links

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PubChem 74959
NPASS NPC271588