Oxacyclotetradecan-2-one, 13-methyl-, (13R)-

Details

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Internal ID 4eb70ce5-ba8b-4adb-8cfd-23e3e12b59cf
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (13R)-13-methyl-oxacyclotetradecan-2-one
SMILES (Canonical) CC1CCCCCCCCCCC(=O)OC1
SMILES (Isomeric) C[C@@H]1CCCCCCCCCCC(=O)OC1
InChI InChI=1S/C14H26O2/c1-13-10-8-6-4-2-3-5-7-9-11-14(15)16-12-13/h13H,2-12H2,1H3/t13-/m1/s1
InChI Key NFNWPPOMMYDNFQ-CYBMUJFWSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C14H26O2
Molecular Weight 226.35 g/mol
Exact Mass 226.193280068 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.08
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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160496-16-2
r-12-methyl-13-tridecanolide
DTXSID90438939

2D Structure

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2D Structure of Oxacyclotetradecan-2-one, 13-methyl-, (13R)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.8588 85.88%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4644 46.44%
OATP2B1 inhibitior - 0.8415 84.15%
OATP1B1 inhibitior + 0.9577 95.77%
OATP1B3 inhibitior + 0.9523 95.23%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6423 64.23%
P-glycoprotein inhibitior - 0.9056 90.56%
P-glycoprotein substrate - 0.9582 95.82%
CYP3A4 substrate - 0.5935 59.35%
CYP2C9 substrate + 0.6131 61.31%
CYP2D6 substrate - 0.8625 86.25%
CYP3A4 inhibition - 0.9595 95.95%
CYP2C9 inhibition - 0.8995 89.95%
CYP2C19 inhibition - 0.8456 84.56%
CYP2D6 inhibition - 0.9555 95.55%
CYP1A2 inhibition - 0.5633 56.33%
CYP2C8 inhibition - 0.9872 98.72%
CYP inhibitory promiscuity - 0.9846 98.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6492 64.92%
Eye corrosion + 0.8643 86.43%
Eye irritation + 0.8987 89.87%
Skin irritation + 0.5435 54.35%
Skin corrosion - 0.9548 95.48%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4823 48.23%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6605 66.05%
skin sensitisation - 0.7206 72.06%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5492 54.92%
Estrogen receptor binding - 0.8148 81.48%
Androgen receptor binding - 0.9387 93.87%
Thyroid receptor binding - 0.6578 65.78%
Glucocorticoid receptor binding - 0.8469 84.69%
Aromatase binding - 0.8422 84.22%
PPAR gamma - 0.7848 78.48%
Honey bee toxicity - 0.8408 84.08%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.8188 81.88%

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 94.75% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.26% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.85% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.78% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.78% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 82.70% 92.50%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.47% 96.77%
CHEMBL3012 Q13946 Phosphodiesterase 7A 81.76% 99.29%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.23% 95.89%

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 archangelica

Cross-Links

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PubChem 10376424
LOTUS LTS0042734
wikiData Q82254791