14-Hydroxy-9-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione

Details

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Internal ID aaa50bc4-8f3e-4641-9eb4-290caadd38cd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name 14-hydroxy-9-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione
SMILES (Canonical) CC1(CCC2C3(C1C(OC3)OC)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C
SMILES (Isomeric) CC1(CCC2C3(C1C(OC3)OC)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C
InChI InChI=1S/C21H28O6/c1-10-11-7-12(22)14-20(8-11,16(10)23)18(24)27-13-5-6-19(2,3)15-17(25-4)26-9-21(13,14)15/h11-15,17,22H,1,5-9H2,2-4H3
InChI Key ANNDQWYMQQILCQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H28O6
Molecular Weight 376.40 g/mol
Exact Mass 376.18858861 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.85
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 14-Hydroxy-9-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9694 96.94%
Caco-2 - 0.5150 51.50%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.7904 79.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8453 84.53%
OATP1B3 inhibitior + 0.9189 91.89%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.8699 86.99%
P-glycoprotein inhibitior - 0.7027 70.27%
P-glycoprotein substrate - 0.5582 55.82%
CYP3A4 substrate + 0.7060 70.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8630 86.30%
CYP3A4 inhibition - 0.6368 63.68%
CYP2C9 inhibition - 0.7441 74.41%
CYP2C19 inhibition - 0.8507 85.07%
CYP2D6 inhibition - 0.9382 93.82%
CYP1A2 inhibition - 0.7384 73.84%
CYP2C8 inhibition - 0.6005 60.05%
CYP inhibitory promiscuity - 0.9424 94.24%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5687 56.87%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9373 93.73%
Skin irritation - 0.5542 55.42%
Skin corrosion - 0.9250 92.50%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4748 47.48%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8254 82.54%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.8807 88.07%
Acute Oral Toxicity (c) I 0.4747 47.47%
Estrogen receptor binding + 0.8569 85.69%
Androgen receptor binding + 0.6695 66.95%
Thyroid receptor binding + 0.6795 67.95%
Glucocorticoid receptor binding + 0.7642 76.42%
Aromatase binding + 0.6820 68.20%
PPAR gamma + 0.6653 66.53%
Honey bee toxicity - 0.7101 71.01%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9883 98.83%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 95.13% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.45% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.73% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.33% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 92.61% 94.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.56% 85.14%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.57% 97.14%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 87.77% 96.38%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.88% 95.56%
CHEMBL1871 P10275 Androgen Receptor 86.37% 96.43%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.69% 91.07%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.27% 100.00%
CHEMBL1902 P62942 FK506-binding protein 1A 84.60% 97.05%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.53% 92.94%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.42% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.63% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.24% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.96% 95.89%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 81.90% 95.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.23% 92.62%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.41% 94.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.28% 97.25%

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.
Isodon serra

Cross-Links

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PubChem 74344390
LOTUS LTS0159642
wikiData Q104915292