(-)-(4S,5S,8R,10R,20S)-8,18-dihydroxy-12-oxo-abieta-9(11),13-dien-20-aldehyde 8,18,20-acetal

Details

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Internal ID 592ea324-3fb2-4dd0-98ae-5896112ff7c8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1R,3S,6S,10R,18S)-6-methyl-14-propan-2-yl-2,4-dioxapentacyclo[8.5.3.01,11.03,10.06,18]octadeca-11,14-dien-13-one
SMILES (Canonical) CC(C)C1=CC23CCC4C5(CCCC4(C2=CC1=O)C(O3)OC5)C
SMILES (Isomeric) CC(C)C1=C[C@]23CC[C@H]4[C@@]5(CCC[C@@]4(C2=CC1=O)[C@H](O3)OC5)C
InChI InChI=1S/C20H26O3/c1-12(2)13-10-19-8-5-15-18(3)6-4-7-20(15,16(19)9-14(13)21)17(23-19)22-11-18/h9-10,12,15,17H,4-8,11H2,1-3H3/t15-,17-,18+,19+,20+/m0/s1
InChI Key OUHYDBUWCBLVQF-LFAQGZIKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H26O3
Molecular Weight 314.40 g/mol
Exact Mass 314.18819469 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.79
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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(-)-(4S,5S,8R,10R,20S)-8,18-dihydroxy-12-oxo-abieta-9(11),13-dien-20-aldehyde 8,18,20-acetal
CHEMBL1651060
Q27138883
(20S)-8,20:19,20-diepoxyabieta-9(11),13-dien-12-one

2D Structure

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2D Structure of (-)-(4S,5S,8R,10R,20S)-8,18-dihydroxy-12-oxo-abieta-9(11),13-dien-20-aldehyde 8,18,20-acetal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.8407 84.07%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8197 81.97%
OATP2B1 inhibitior - 0.8641 86.41%
OATP1B1 inhibitior + 0.8866 88.66%
OATP1B3 inhibitior + 0.9799 97.99%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior - 0.6103 61.03%
P-glycoprotein inhibitior - 0.7151 71.51%
P-glycoprotein substrate - 0.7416 74.16%
CYP3A4 substrate + 0.6412 64.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8602 86.02%
CYP3A4 inhibition - 0.8571 85.71%
CYP2C9 inhibition - 0.8738 87.38%
CYP2C19 inhibition - 0.7983 79.83%
CYP2D6 inhibition - 0.9001 90.01%
CYP1A2 inhibition - 0.6912 69.12%
CYP2C8 inhibition - 0.7033 70.33%
CYP inhibitory promiscuity - 0.8682 86.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5660 56.60%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9675 96.75%
Skin irritation - 0.6432 64.32%
Skin corrosion - 0.9365 93.65%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3793 37.93%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5232 52.32%
skin sensitisation - 0.6911 69.11%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.5996 59.96%
Acute Oral Toxicity (c) III 0.6173 61.73%
Estrogen receptor binding + 0.8054 80.54%
Androgen receptor binding + 0.7132 71.32%
Thyroid receptor binding + 0.6722 67.22%
Glucocorticoid receptor binding + 0.7577 75.77%
Aromatase binding + 0.7287 72.87%
PPAR gamma + 0.7322 73.22%
Honey bee toxicity - 0.8245 82.45%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9903 99.03%

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 96.29% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.78% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.35% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.42% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.28% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.28% 99.23%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.95% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.11% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.89% 100.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.70% 85.30%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.38% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 86.03% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.71% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.55% 97.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.43% 96.77%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.36% 93.04%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.03% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.84% 93.56%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.08% 95.71%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.50% 91.07%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.28% 92.62%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.12% 82.69%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.86% 90.08%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 81.21% 85.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.70% 90.71%

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.
Fraxinus sieboldiana

Cross-Links

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PubChem 50900414
LOTUS LTS0082781
wikiData Q27138883