Oxacyclohexadecan-2-one

Details

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Internal ID 5bd503d6-6bd1-4490-a1c4-ada66733ef4c
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name oxacyclohexadecan-2-one
SMILES (Canonical) C1CCCCCCCOC(=O)CCCCCC1
SMILES (Isomeric) C1CCCCCCCOC(=O)CCCCCC1
InChI InChI=1S/C15H28O2/c16-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-17-15/h1-14H2
InChI Key FKUPPRZPSYCDRS-UHFFFAOYSA-N
Popularity 220 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28O2
Molecular Weight 240.38 g/mol
Exact Mass 240.208930132 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.61
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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106-02-5
Cyclopentadecanolide
Pentadecanolide
Exaltolide
Pentalide
15-Pentadecanolide
Pentadecan-15-olide
PENTADECALACTONE
Muskolactone
Thibetolide
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Oxacyclohexadecan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.6792 67.92%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.6628 66.28%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.9707 97.07%
OATP1B3 inhibitior + 0.9599 95.99%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6930 69.30%
P-glycoprotein inhibitior - 0.9476 94.76%
P-glycoprotein substrate - 0.9932 99.32%
CYP3A4 substrate - 0.7088 70.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8330 83.30%
CYP3A4 inhibition - 0.9849 98.49%
CYP2C9 inhibition - 0.8693 86.93%
CYP2C19 inhibition - 0.8772 87.72%
CYP2D6 inhibition - 0.9637 96.37%
CYP1A2 inhibition - 0.8747 87.47%
CYP2C8 inhibition - 0.9947 99.47%
CYP inhibitory promiscuity - 0.9831 98.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6738 67.38%
Eye corrosion + 0.9854 98.54%
Eye irritation + 0.9882 98.82%
Skin irritation - 0.5475 54.75%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4039 40.39%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.9400 94.00%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.9542 95.42%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.5217 52.17%
Acute Oral Toxicity (c) III 0.8003 80.03%
Estrogen receptor binding - 0.8743 87.43%
Androgen receptor binding - 0.9127 91.27%
Thyroid receptor binding - 0.8078 80.78%
Glucocorticoid receptor binding - 0.8480 84.80%
Aromatase binding - 0.7098 70.98%
PPAR gamma - 0.6814 68.14%
Honey bee toxicity - 0.9241 92.41%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.6465 64.65%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.10% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.18% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.80% 96.77%

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.
Angelica acutiloba
Angelica archangelica
Angelica dahurica
Angelica gigas
Angelica sinensis
Lonicera japonica
Tetradium ruticarpum

Cross-Links

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PubChem 235414
NPASS NPC223249
LOTUS LTS0107598
wikiData Q9251595