[(1R,2R,3R,4S,6R,7S,9R,10S,11S,13S)-2-acetyloxy-3,6,11-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-7-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate

Details

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Internal ID ec076aee-f1b1-4c81-afbe-b9a7fdd349da
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name [(1R,2R,3R,4S,6R,7S,9R,10S,11S,13S)-2-acetyloxy-3,6,11-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-7-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate
SMILES (Canonical) CC(=O)OC1CC2(C3C(CC4CC3(C(C(C2C(C1O)(C)C)O)OC(=O)C)C(=O)C4=C)O)C
SMILES (Isomeric) CC(=O)O[C@H]1C[C@@]2([C@@H]3[C@H](C[C@@H]4C[C@@]3([C@H]([C@@H]([C@@H]2C([C@H]1O)(C)C)O)OC(=O)C)C(=O)C4=C)O)C
InChI InChI=1S/C24H34O8/c1-10-13-7-14(27)17-23(6)9-15(31-11(2)25)20(30)22(4,5)18(23)16(28)21(32-12(3)26)24(17,8-13)19(10)29/h13-18,20-21,27-28,30H,1,7-9H2,2-6H3/t13-,14+,15+,16-,17+,18-,20+,21+,23-,24+/m1/s1
InChI Key HPJIOIQEFOBADG-SQHUPIIUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H34O8
Molecular Weight 450.50 g/mol
Exact Mass 450.22536804 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.15
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,2R,3R,4S,6R,7S,9R,10S,11S,13S)-2-acetyloxy-3,6,11-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-7-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9848 98.48%
Caco-2 - 0.7461 74.61%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7245 72.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8746 87.46%
OATP1B3 inhibitior - 0.2433 24.33%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6930 69.30%
P-glycoprotein inhibitior - 0.5645 56.45%
P-glycoprotein substrate - 0.7708 77.08%
CYP3A4 substrate + 0.6628 66.28%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8731 87.31%
CYP3A4 inhibition - 0.7091 70.91%
CYP2C9 inhibition - 0.7814 78.14%
CYP2C19 inhibition - 0.7566 75.66%
CYP2D6 inhibition - 0.9480 94.80%
CYP1A2 inhibition - 0.8515 85.15%
CYP2C8 inhibition - 0.7323 73.23%
CYP inhibitory promiscuity - 0.9143 91.43%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5646 56.46%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9179 91.79%
Skin irritation - 0.5651 56.51%
Skin corrosion - 0.9367 93.67%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6266 62.66%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.5542 55.42%
skin sensitisation - 0.6433 64.33%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.8065 80.65%
Acute Oral Toxicity (c) I 0.4350 43.50%
Estrogen receptor binding + 0.7533 75.33%
Androgen receptor binding + 0.6123 61.23%
Thyroid receptor binding - 0.5472 54.72%
Glucocorticoid receptor binding + 0.7097 70.97%
Aromatase binding + 0.6156 61.56%
PPAR gamma + 0.5770 57.70%
Honey bee toxicity - 0.6256 62.56%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9955 99.55%

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 95.65% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.01% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.76% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.98% 85.14%
CHEMBL221 P23219 Cyclooxygenase-1 92.36% 90.17%
CHEMBL2581 P07339 Cathepsin D 89.24% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 88.75% 91.19%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.23% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.66% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.69% 96.77%
CHEMBL259 P32245 Melanocortin receptor 4 86.66% 95.38%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.62% 93.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.61% 97.25%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.70% 91.07%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.96% 95.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.59% 100.00%
CHEMBL1951 P21397 Monoamine oxidase A 82.65% 91.49%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.77% 94.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.68% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.67% 95.56%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 80.05% 91.24%

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 angustifolius

Cross-Links

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PubChem 162890038
LOTUS LTS0153477
wikiData Q105031726