(9,14-Dihydroxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-18-yl) acetate

Details

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Internal ID c2288e29-9506-49dd-9c67-7041d7ca3703
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name (9,14-dihydroxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-18-yl) acetate
SMILES (Canonical) CC(=O)OC1C(=C)C2CC(C3C1(C2)C(=O)OC4C35COC(C5C(CC4)(C)C)O)O
SMILES (Isomeric) CC(=O)OC1C(=C)C2CC(C3C1(C2)C(=O)OC4C35COC(C5C(CC4)(C)C)O)O
InChI InChI=1S/C22H30O7/c1-10-12-7-13(24)15-21(8-12,17(10)28-11(2)23)19(26)29-14-5-6-20(3,4)16-18(25)27-9-22(14,15)16/h12-18,24-25H,1,5-9H2,2-4H3
InChI Key JUJKSMRAYVDOKO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H30O7
Molecular Weight 406.50 g/mol
Exact Mass 406.19915329 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.56
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (9,14-Dihydroxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-18-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9750 97.50%
Caco-2 - 0.5973 59.73%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8330 83.30%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8425 84.25%
OATP1B3 inhibitior + 0.8678 86.78%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7146 71.46%
BSEP inhibitior - 0.6700 67.00%
P-glycoprotein inhibitior - 0.6358 63.58%
P-glycoprotein substrate + 0.5178 51.78%
CYP3A4 substrate + 0.7201 72.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8665 86.65%
CYP3A4 inhibition - 0.6933 69.33%
CYP2C9 inhibition - 0.7069 70.69%
CYP2C19 inhibition - 0.8770 87.70%
CYP2D6 inhibition - 0.9426 94.26%
CYP1A2 inhibition - 0.7982 79.82%
CYP2C8 inhibition - 0.5969 59.69%
CYP inhibitory promiscuity - 0.9309 93.09%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5633 56.33%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9211 92.11%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9275 92.75%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5778 57.78%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.5700 57.00%
skin sensitisation - 0.8361 83.61%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.8343 83.43%
Acute Oral Toxicity (c) I 0.4907 49.07%
Estrogen receptor binding + 0.8127 81.27%
Androgen receptor binding + 0.6600 66.00%
Thyroid receptor binding + 0.5832 58.32%
Glucocorticoid receptor binding + 0.7566 75.66%
Aromatase binding + 0.6520 65.20%
PPAR gamma + 0.5702 57.02%
Honey bee toxicity - 0.6648 66.48%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9950 99.50%

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 95.58% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.91% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 91.81% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.42% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.13% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 90.31% 91.19%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.96% 97.14%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 89.84% 96.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.55% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.47% 99.23%
CHEMBL2581 P07339 Cathepsin D 87.32% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.13% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.47% 89.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.14% 97.25%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.35% 91.07%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 83.10% 95.71%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.71% 93.03%
CHEMBL1871 P10275 Androgen Receptor 82.13% 96.43%
CHEMBL259 P32245 Melanocortin receptor 4 81.86% 95.38%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.65% 98.75%
CHEMBL2803 P43403 Tyrosine-protein kinase ZAP-70 81.28% 82.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.12% 95.56%

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 henryi

Cross-Links

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PubChem 78385461
LOTUS LTS0236372
wikiData Q105135268