(Z)-5-[(1R,4aS,5R,8aS)-5-(acetyloxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-(acetyloxymethyl)pent-2-enoic acid

Details

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Internal ID bfcf178d-4ebf-4e0e-806a-026f0e15e8c4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (Z)-5-[(1R,4aS,5R,8aS)-5-(acetyloxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-(acetyloxymethyl)pent-2-enoic acid
SMILES (Canonical) CC(=O)OCC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)COC(=O)C)C
SMILES (Isomeric) CC(=O)OC/C(=C\C(=O)O)/CC[C@@H]1C(=C)CC[C@H]2[C@]1(CCC[C@@]2(C)COC(=O)C)C
InChI InChI=1S/C24H36O6/c1-16-7-10-21-23(4,15-30-18(3)26)11-6-12-24(21,5)20(16)9-8-19(13-22(27)28)14-29-17(2)25/h13,20-21H,1,6-12,14-15H2,2-5H3,(H,27,28)/b19-13-/t20-,21-,23+,24+/m1/s1
InChI Key UIKODHRRIJEZLZ-QHIXUVDYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H36O6
Molecular Weight 420.50 g/mol
Exact Mass 420.25118886 g/mol
Topological Polar Surface Area (TPSA) 89.90 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.68
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-5-[(1R,4aS,5R,8aS)-5-(acetyloxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-(acetyloxymethyl)pent-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9607 96.07%
Caco-2 - 0.5748 57.48%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7463 74.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8280 82.80%
OATP1B3 inhibitior + 0.8431 84.31%
MATE1 inhibitior - 0.6400 64.00%
OCT2 inhibitior - 0.6271 62.71%
BSEP inhibitior + 0.8945 89.45%
P-glycoprotein inhibitior + 0.6585 65.85%
P-glycoprotein substrate - 0.7133 71.33%
CYP3A4 substrate + 0.6545 65.45%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.9167 91.67%
CYP3A4 inhibition - 0.6703 67.03%
CYP2C9 inhibition - 0.7406 74.06%
CYP2C19 inhibition - 0.7395 73.95%
CYP2D6 inhibition - 0.8990 89.90%
CYP1A2 inhibition - 0.7571 75.71%
CYP2C8 inhibition + 0.5739 57.39%
CYP inhibitory promiscuity - 0.7301 73.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6279 62.79%
Eye corrosion - 0.9783 97.83%
Eye irritation - 0.8143 81.43%
Skin irritation - 0.5891 58.91%
Skin corrosion - 0.9791 97.91%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3703 37.03%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.5857 58.57%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.8237 82.37%
Acute Oral Toxicity (c) III 0.7292 72.92%
Estrogen receptor binding + 0.7793 77.93%
Androgen receptor binding + 0.6910 69.10%
Thyroid receptor binding - 0.4944 49.44%
Glucocorticoid receptor binding + 0.8045 80.45%
Aromatase binding + 0.7162 71.62%
PPAR gamma + 0.7012 70.12%
Honey bee toxicity - 0.7847 78.47%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6755 67.55%
Fish aquatic toxicity + 1.0000 100.00%

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 96.14% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.55% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.40% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 88.20% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.08% 95.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.53% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.28% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 87.22% 91.19%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.90% 95.50%
CHEMBL5028 O14672 ADAM10 85.21% 97.50%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 84.54% 96.38%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.39% 86.33%
CHEMBL2061 P19793 Retinoid X receptor alpha 83.28% 91.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.96% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.90% 95.89%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.88% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.66% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.32% 82.69%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.37% 99.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.35% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.00% 97.09%

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.
Leiocarpa semicalva

Cross-Links

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PubChem 162912796
LOTUS LTS0005071
wikiData Q105273419