(+)-(5S,6S,10R)-12-hydroxy-7-oxo-abieta-8,11,13-trien-20-oic acid6,20-lactone

Details

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Internal ID bdc25ca5-0072-482d-8d90-79df4dad95fb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name (1R,9S,10S)-4-hydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-triene-8,15-dione
SMILES (Canonical) CC(C)C1=C(C=C2C(=C1)C(=O)C3C4C2(CCCC4(C)C)C(=O)O3)O
SMILES (Isomeric) CC(C)C1=C(C=C2C(=C1)C(=O)[C@@H]3[C@@H]4[C@@]2(CCCC4(C)C)C(=O)O3)O
InChI InChI=1S/C20H24O4/c1-10(2)11-8-12-13(9-14(11)21)20-7-5-6-19(3,4)17(20)16(15(12)22)24-18(20)23/h8-10,16-17,21H,5-7H2,1-4H3/t16-,17+,20+/m1/s1
InChI Key VUAJCLNFGUYDIL-UWVAXJGDSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H24O4
Molecular Weight 328.40 g/mol
Exact Mass 328.16745924 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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(+)-(5S,6S,10R)-12-hydroxy-7-oxo-abieta-8,11,13-trien-20-oic acid6,20-lactone
CHEMBL1651065
Q27138889
(6alpha)-12-hydroxy-6,20-epoxyabieta-8,11,13-triene-7,20-dione

2D Structure

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2D Structure of (+)-(5S,6S,10R)-12-hydroxy-7-oxo-abieta-8,11,13-trien-20-oic acid6,20-lactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9867 98.67%
Caco-2 + 0.7249 72.49%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7556 75.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8596 85.96%
OATP1B3 inhibitior + 0.8990 89.90%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9020 90.20%
P-glycoprotein inhibitior - 0.7983 79.83%
P-glycoprotein substrate - 0.7815 78.15%
CYP3A4 substrate + 0.6167 61.67%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8334 83.34%
CYP3A4 inhibition - 0.8007 80.07%
CYP2C9 inhibition - 0.6454 64.54%
CYP2C19 inhibition - 0.7568 75.68%
CYP2D6 inhibition - 0.9045 90.45%
CYP1A2 inhibition + 0.6230 62.30%
CYP2C8 inhibition - 0.8156 81.56%
CYP inhibitory promiscuity - 0.9256 92.56%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5741 57.41%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.8400 84.00%
Skin irritation - 0.6381 63.81%
Skin corrosion - 0.8529 85.29%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8445 84.45%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5553 55.53%
skin sensitisation - 0.8266 82.66%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.5926 59.26%
Acute Oral Toxicity (c) III 0.6044 60.44%
Estrogen receptor binding + 0.8305 83.05%
Androgen receptor binding + 0.6005 60.05%
Thyroid receptor binding + 0.6291 62.91%
Glucocorticoid receptor binding + 0.8393 83.93%
Aromatase binding + 0.7568 75.68%
PPAR gamma + 0.7824 78.24%
Honey bee toxicity - 0.9019 90.19%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9966 99.66%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.44% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.54% 99.15%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.26% 96.77%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 92.83% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.60% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.04% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 90.49% 94.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.95% 96.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.62% 90.71%
CHEMBL3286 P00749 Urokinase-type plasminogen activator 87.34% 97.88%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.56% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.81% 82.69%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.46% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.86% 86.33%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.21% 93.04%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.46% 93.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.28% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.21% 95.89%
CHEMBL2535 P11166 Glucose transporter 82.97% 98.75%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.74% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.05% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.39% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.34% 95.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.06% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.05% 93.03%
CHEMBL3401 O75469 Pregnane X receptor 80.34% 94.73%

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 50900507
LOTUS LTS0256814
wikiData Q27138889