Plagiochiline N

Details

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Internal ID 0cd2a340-9e15-431f-9ea8-16daa1c4a87c
Taxonomy Organoheterocyclic compounds > Cycloheptapyrans
IUPAC Name (1S,2S,4S)-3,3,7,12-tetramethyl-10-oxatricyclo[6.4.0.02,4]dodeca-6,8,11-triene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O/c1-9-5-6-12-14(15(12,3)4)13-10(2)7-16-8-11(9)13/h5,7-8,12-14H,6H2,1-4H3/t12-,13-,14-/m0/s1
InChI Key QBJIOYPULQIUMZ-IHRRRGAJSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O
Molecular Weight 216.32 g/mol
Exact Mass 216.151415257 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 4.04
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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(1S,2S,4S)-3,3,7,12-Tetramethyl-10-oxatricyclo[6.4.0.02,4]dodeca-6,8,11-triene

2D Structure

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2D Structure of Plagiochiline N

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.7919 79.19%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.7351 73.51%
OATP2B1 inhibitior - 0.8621 86.21%
OATP1B1 inhibitior + 0.8983 89.83%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8329 83.29%
P-glycoprotein inhibitior - 0.9412 94.12%
P-glycoprotein substrate - 0.8272 82.72%
CYP3A4 substrate + 0.5265 52.65%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7665 76.65%
CYP3A4 inhibition - 0.8997 89.97%
CYP2C9 inhibition - 0.7089 70.89%
CYP2C19 inhibition - 0.5617 56.17%
CYP2D6 inhibition - 0.8859 88.59%
CYP1A2 inhibition - 0.5467 54.67%
CYP2C8 inhibition - 0.6502 65.02%
CYP inhibitory promiscuity - 0.7295 72.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7036 70.36%
Carcinogenicity (trinary) Non-required 0.5786 57.86%
Eye corrosion - 0.9047 90.47%
Eye irritation + 0.7832 78.32%
Skin irritation + 0.6123 61.23%
Skin corrosion - 0.8938 89.38%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8156 81.56%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.6594 65.94%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.6662 66.62%
Acute Oral Toxicity (c) III 0.7190 71.90%
Estrogen receptor binding - 0.6115 61.15%
Androgen receptor binding + 0.5549 55.49%
Thyroid receptor binding - 0.6556 65.56%
Glucocorticoid receptor binding - 0.8256 82.56%
Aromatase binding - 0.8099 80.99%
PPAR gamma - 0.5432 54.32%
Honey bee toxicity - 0.7808 78.08%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.8599 85.99%

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 91.07% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.45% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.36% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 84.91% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.66% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.82% 86.33%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 82.37% 89.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.09% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.06% 95.56%

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.
Plagiochila ovalifolia

Cross-Links

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PubChem 11148642
LOTUS LTS0122444
wikiData Q105217843