(1S,2S,5R,6R,8S,11S,14R,17S,20R)-6,14-dimethyl-10,16,18-trioxahexacyclo[12.5.1.15,8.01,11.02,8.017,20]henicosan-9-one

Details

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Internal ID f40edef8-bd63-40b8-96b1-2569b7ef77f5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name (1S,2S,5R,6R,8S,11S,14R,17S,20R)-6,14-dimethyl-10,16,18-trioxahexacyclo[12.5.1.15,8.01,11.02,8.017,20]henicosan-9-one
SMILES (Canonical) CC1CC23CC1CCC2C45COC6C4C(CCC5OC3=O)(CO6)C
SMILES (Isomeric) C[C@@H]1C[C@]23C[C@H]1CC[C@H]2[C@@]45CO[C@H]6[C@@H]4[C@@](CC[C@@H]5OC3=O)(CO6)C
InChI InChI=1S/C20H28O4/c1-11-7-19-8-12(11)3-4-13(19)20-10-23-16-15(20)18(2,9-22-16)6-5-14(20)24-17(19)21/h11-16H,3-10H2,1-2H3/t11-,12-,13-,14+,15-,16+,18+,19+,20-/m1/s1
InChI Key KNPACDIMHORWGX-UUCILADCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O4
Molecular Weight 332.40 g/mol
Exact Mass 332.19875937 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,2S,5R,6R,8S,11S,14R,17S,20R)-6,14-dimethyl-10,16,18-trioxahexacyclo[12.5.1.15,8.01,11.02,8.017,20]henicosan-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9752 97.52%
Caco-2 + 0.7067 70.67%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6173 61.73%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9169 91.69%
OATP1B3 inhibitior + 0.9651 96.51%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.7064 70.64%
P-glycoprotein inhibitior - 0.7431 74.31%
P-glycoprotein substrate - 0.6976 69.76%
CYP3A4 substrate + 0.6373 63.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8195 81.95%
CYP3A4 inhibition - 0.9291 92.91%
CYP2C9 inhibition - 0.8941 89.41%
CYP2C19 inhibition - 0.8077 80.77%
CYP2D6 inhibition - 0.9078 90.78%
CYP1A2 inhibition - 0.8370 83.70%
CYP2C8 inhibition - 0.7075 70.75%
CYP inhibitory promiscuity - 0.9643 96.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6270 62.70%
Eye corrosion - 0.9771 97.71%
Eye irritation - 0.9593 95.93%
Skin irritation - 0.8104 81.04%
Skin corrosion - 0.9173 91.73%
Ames mutagenesis + 0.5036 50.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5765 57.65%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.5069 50.69%
skin sensitisation - 0.9055 90.55%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5689 56.89%
Estrogen receptor binding + 0.8498 84.98%
Androgen receptor binding + 0.5823 58.23%
Thyroid receptor binding + 0.6191 61.91%
Glucocorticoid receptor binding + 0.6206 62.06%
Aromatase binding + 0.6354 63.54%
PPAR gamma + 0.6153 61.53%
Honey bee toxicity - 0.7467 74.67%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.8100 81.00%
Fish aquatic toxicity + 0.9103 91.03%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.96% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.73% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.27% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 88.65% 94.75%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.56% 92.94%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.48% 96.61%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.59% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.41% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.26% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.91% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 84.70% 95.71%
CHEMBL325 Q13547 Histone deacetylase 1 84.70% 95.92%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.33% 97.14%
CHEMBL221 P23219 Cyclooxygenase-1 83.70% 90.17%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.59% 96.77%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 83.47% 94.78%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.36% 93.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.48% 93.04%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.17% 89.00%
CHEMBL4072 P07858 Cathepsin B 80.98% 93.67%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.75% 94.45%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.72% 96.38%

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 rubescens

Cross-Links

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PubChem 101235551
LOTUS LTS0129764
wikiData Q105143502