Propanoic acid, 2,2-dimethyl-, phenylmethyl ester

Details

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Internal ID a6bdb31d-3e2c-4cf9-b9e6-23f52c278425
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyloxycarbonyls
IUPAC Name benzyl 2,2-dimethylpropanoate
SMILES (Canonical) CC(C)(C)C(=O)OCC1=CC=CC=C1
SMILES (Isomeric) CC(C)(C)C(=O)OCC1=CC=CC=C1
InChI InChI=1S/C12H16O2/c1-12(2,3)11(13)14-9-10-7-5-4-6-8-10/h4-8H,9H2,1-3H3
InChI Key QCFKLVCBTZKWGY-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O2
Molecular Weight 192.25 g/mol
Exact Mass 192.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Benzyl pivalate
2094-69-1
PROPANOIC ACID, 2,2-DIMETHYL-, PHENYLMETHYL ESTER
Pivalic acid, benzyl ester
Benzyl 2,2-dimethylpropionate
NSC-409387
Cbz-tBu
Benzyl pivalate #
UPCMLD00WJLM9
6PLV4J9C6P
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Propanoic acid, 2,2-dimethyl-, phenylmethyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.8507 85.07%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7976 79.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9261 92.61%
OATP1B3 inhibitior + 0.9295 92.95%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6549 65.49%
P-glycoprotein inhibitior - 0.9872 98.72%
P-glycoprotein substrate - 0.9855 98.55%
CYP3A4 substrate - 0.6212 62.12%
CYP2C9 substrate - 0.8246 82.46%
CYP2D6 substrate - 0.8209 82.09%
CYP3A4 inhibition - 0.9217 92.17%
CYP2C9 inhibition - 0.8672 86.72%
CYP2C19 inhibition - 0.8890 88.90%
CYP2D6 inhibition - 0.9214 92.14%
CYP1A2 inhibition + 0.5082 50.82%
CYP2C8 inhibition - 0.8042 80.42%
CYP inhibitory promiscuity - 0.7114 71.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5244 52.44%
Carcinogenicity (trinary) Non-required 0.5067 50.67%
Eye corrosion + 0.6201 62.01%
Eye irritation + 0.7689 76.89%
Skin irritation - 0.5363 53.63%
Skin corrosion - 0.9742 97.42%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5897 58.97%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5926 59.26%
skin sensitisation + 0.7875 78.75%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.9039 90.39%
Nephrotoxicity - 0.5630 56.30%
Acute Oral Toxicity (c) III 0.6960 69.60%
Estrogen receptor binding - 0.5546 55.46%
Androgen receptor binding - 0.7444 74.44%
Thyroid receptor binding - 0.8667 86.67%
Glucocorticoid receptor binding - 0.8193 81.93%
Aromatase binding - 0.4828 48.28%
PPAR gamma - 0.8127 81.27%
Honey bee toxicity - 0.9503 95.03%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9381 93.81%

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
CHEMBL2581 P07339 Cathepsin D 96.07% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.20% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.61% 99.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.39% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.81% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.34% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 84.80% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.03% 95.50%

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.
Artemisia annua
Artemisia carvifolia

Cross-Links

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PubChem 74977
NPASS NPC278685