(11-Hydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl acetate

Details

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Internal ID b4ec6693-843d-4180-b574-e37638a5d208
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name (11-hydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl acetate
SMILES (Canonical) CC(=O)OCC1(CCCC2(C1CCC34C2C(CC(C3)C(=C)C4=O)O)C)C
SMILES (Isomeric) CC(=O)OCC1(CCCC2(C1CCC34C2C(CC(C3)C(=C)C4=O)O)C)C
InChI InChI=1S/C22H32O4/c1-13-15-10-16(24)18-21(4)8-5-7-20(3,12-26-14(2)23)17(21)6-9-22(18,11-15)19(13)25/h15-18,24H,1,5-12H2,2-4H3
InChI Key BNDIEBQEHNGNLK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H32O4
Molecular Weight 360.50 g/mol
Exact Mass 360.23005950 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (11-Hydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.6166 61.66%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7841 78.41%
OATP2B1 inhibitior - 0.8669 86.69%
OATP1B1 inhibitior + 0.8159 81.59%
OATP1B3 inhibitior + 0.9356 93.56%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5021 50.21%
BSEP inhibitior - 0.4718 47.18%
P-glycoprotein inhibitior - 0.6892 68.92%
P-glycoprotein substrate - 0.7269 72.69%
CYP3A4 substrate + 0.6853 68.53%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8731 87.31%
CYP3A4 inhibition - 0.7545 75.45%
CYP2C9 inhibition - 0.8293 82.93%
CYP2C19 inhibition - 0.9086 90.86%
CYP2D6 inhibition - 0.9257 92.57%
CYP1A2 inhibition - 0.8445 84.45%
CYP2C8 inhibition - 0.6321 63.21%
CYP inhibitory promiscuity - 0.8837 88.37%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6921 69.21%
Eye corrosion - 0.9932 99.32%
Eye irritation - 0.8846 88.46%
Skin irritation + 0.6709 67.09%
Skin corrosion - 0.9608 96.08%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4600 46.00%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.6573 65.73%
skin sensitisation - 0.8482 84.82%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5615 56.15%
Acute Oral Toxicity (c) III 0.8055 80.55%
Estrogen receptor binding + 0.8055 80.55%
Androgen receptor binding + 0.6658 66.58%
Thyroid receptor binding + 0.5783 57.83%
Glucocorticoid receptor binding + 0.8519 85.19%
Aromatase binding + 0.6322 63.22%
PPAR gamma + 0.5242 52.42%
Honey bee toxicity - 0.7486 74.86%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5200 52.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.49% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.18% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 95.03% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.64% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.81% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 90.45% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.33% 97.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 89.82% 96.38%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.62% 94.45%
CHEMBL1902 P62942 FK506-binding protein 1A 87.70% 97.05%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.76% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 84.52% 91.19%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.75% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.33% 86.33%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.03% 95.50%
CHEMBL259 P32245 Melanocortin receptor 4 82.27% 95.38%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.07% 90.08%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.05% 100.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.58% 94.33%
CHEMBL1937 Q92769 Histone deacetylase 2 81.53% 94.75%
CHEMBL5255 O00206 Toll-like receptor 4 81.24% 92.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.66% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.45% 93.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.41% 93.04%

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.
Croton kongensis

Cross-Links

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PubChem 72781632
LOTUS LTS0129551
wikiData Q104938733