(+)-15-Beyeren-3-one

Details

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Internal ID 586ffc26-ff23-419b-933a-481c262b82ee
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1R,4S,9S,10S,13S)-5,5,9,13-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-6-one
SMILES (Canonical) CC1(C2CCC34CC(CCC3C2(CCC1=O)C)(C=C4)C)C
SMILES (Isomeric) C[C@]12CC[C@H]3[C@@]4(CCC(=O)C([C@H]4CC[C@@]3(C1)C=C2)(C)C)C
InChI InChI=1S/C20H30O/c1-17(2)14-6-10-20-12-11-18(3,13-20)8-5-15(20)19(14,4)9-7-16(17)21/h11-12,14-15H,5-10,13H2,1-4H3/t14-,15+,18-,19-,20+/m1/s1
InChI Key XRTFKEQRSMHTMN-DGWIIEBVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O
Molecular Weight 286.50 g/mol
Exact Mass 286.229665576 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.15
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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LMPR0104140002

2D Structure

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2D Structure of (+)-15-Beyeren-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.8442 84.42%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.4814 48.14%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.9154 91.54%
OATP1B3 inhibitior + 0.9678 96.78%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.5942 59.42%
P-glycoprotein inhibitior - 0.6326 63.26%
P-glycoprotein substrate - 0.9118 91.18%
CYP3A4 substrate + 0.5374 53.74%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8099 80.99%
CYP3A4 inhibition - 0.9036 90.36%
CYP2C9 inhibition - 0.8501 85.01%
CYP2C19 inhibition - 0.6841 68.41%
CYP2D6 inhibition - 0.9655 96.55%
CYP1A2 inhibition - 0.8169 81.69%
CYP2C8 inhibition - 0.8598 85.98%
CYP inhibitory promiscuity - 0.8838 88.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5512 55.12%
Eye corrosion - 0.9694 96.94%
Eye irritation - 0.8735 87.35%
Skin irritation + 0.6617 66.17%
Skin corrosion - 0.9627 96.27%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4309 43.09%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6031 60.31%
skin sensitisation + 0.8331 83.31%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.5106 51.06%
Acute Oral Toxicity (c) III 0.6758 67.58%
Estrogen receptor binding + 0.7158 71.58%
Androgen receptor binding + 0.6118 61.18%
Thyroid receptor binding + 0.6480 64.80%
Glucocorticoid receptor binding + 0.6435 64.35%
Aromatase binding + 0.6516 65.16%
PPAR gamma - 0.5870 58.70%
Honey bee toxicity - 0.8608 86.08%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9891 98.91%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.80% 83.82%
CHEMBL1937 Q92769 Histone deacetylase 2 87.78% 94.75%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.60% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.71% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.41% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.34% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.25% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.32% 91.11%
CHEMBL4072 P07858 Cathepsin B 85.15% 93.67%
CHEMBL2581 P07339 Cathepsin D 84.45% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.82% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.86% 95.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.92% 85.30%

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.
Excoecaria agallocha
Excoecaria parvifolia
Spirostachys africana

Cross-Links

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PubChem 15381927
LOTUS LTS0029412
wikiData Q76506615