[(1S,2S,4S,5R,6R,7S,8R,9R,12R)-4,5-dibenzoyloxy-2,8-dihydroxy-2,6,10,10-tetramethyl-7-(2-methylbutanoyloxy)-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl] furan-3-carboxylate

Details

Top
Internal ID b32a6b00-449a-4f33-a9fe-1b6ea7c65e21
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Agarofurans
IUPAC Name [(1S,2S,4S,5R,6R,7S,8R,9R,12R)-4,5-dibenzoyloxy-2,8-dihydroxy-2,6,10,10-tetramethyl-7-(2-methylbutanoyloxy)-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl] furan-3-carboxylate
SMILES (Canonical) CCC(C)C(=O)OC1C(C2C(C3(C1(C(C(CC3(C)O)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C)OC2(C)C)OC(=O)C6=COC=C6)O
SMILES (Isomeric) CCC(C)C(=O)O[C@@H]1[C@@H]([C@@H]2[C@H]([C@]3([C@]1([C@H]([C@H](C[C@]3(C)O)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C)OC2(C)C)OC(=O)C6=COC=C6)O
InChI InChI=1S/C39H44O12/c1-7-22(2)32(41)50-31-28(40)27-30(49-35(44)25-18-19-46-21-25)39(51-36(27,3)4)37(5,45)20-26(47-33(42)23-14-10-8-11-15-23)29(38(31,39)6)48-34(43)24-16-12-9-13-17-24/h8-19,21-22,26-31,40,45H,7,20H2,1-6H3/t22?,26-,27+,28+,29-,30+,31+,37-,38-,39-/m0/s1
InChI Key XHIFLJAPZSCIEQ-DMFUPTNHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C39H44O12
Molecular Weight 704.80 g/mol
Exact Mass 704.28327683 g/mol
Topological Polar Surface Area (TPSA) 168.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.91
H-Bond Acceptor 12
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [(1S,2S,4S,5R,6R,7S,8R,9R,12R)-4,5-dibenzoyloxy-2,8-dihydroxy-2,6,10,10-tetramethyl-7-(2-methylbutanoyloxy)-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl] furan-3-carboxylate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9749 97.49%
Caco-2 - 0.8088 80.88%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5838 58.38%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.8004 80.04%
OATP1B3 inhibitior - 0.2253 22.53%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9800 98.00%
P-glycoprotein inhibitior + 0.8950 89.50%
P-glycoprotein substrate + 0.5332 53.32%
CYP3A4 substrate + 0.6803 68.03%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8547 85.47%
CYP3A4 inhibition - 0.6316 63.16%
CYP2C9 inhibition - 0.7648 76.48%
CYP2C19 inhibition - 0.8110 81.10%
CYP2D6 inhibition - 0.9399 93.99%
CYP1A2 inhibition - 0.8830 88.30%
CYP2C8 inhibition + 0.7350 73.50%
CYP inhibitory promiscuity - 0.8334 83.34%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4028 40.28%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.9038 90.38%
Skin irritation - 0.7705 77.05%
Skin corrosion - 0.9302 93.02%
Ames mutagenesis - 0.5337 53.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7798 77.98%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.7862 78.62%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7937 79.37%
Acute Oral Toxicity (c) III 0.5575 55.75%
Estrogen receptor binding + 0.7837 78.37%
Androgen receptor binding + 0.7293 72.93%
Thyroid receptor binding + 0.6352 63.52%
Glucocorticoid receptor binding + 0.7489 74.89%
Aromatase binding + 0.6103 61.03%
PPAR gamma + 0.7474 74.74%
Honey bee toxicity - 0.8325 83.25%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5155 51.55%
Fish aquatic toxicity + 0.9820 98.20%

Targets

Top

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
CHEMBL221 P23219 Cyclooxygenase-1 99.58% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.57% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.98% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.01% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.55% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 92.24% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.70% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.07% 99.23%
CHEMBL2535 P11166 Glucose transporter 87.58% 98.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.44% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.05% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.71% 89.00%
CHEMBL5028 O14672 ADAM10 82.63% 97.50%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 81.28% 83.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.25% 96.47%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.87% 97.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.56% 95.50%

Plants that contains it

Top
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.
Celastrus glaucophyllus

Cross-Links

Top
PubChem 101624013
LOTUS LTS0081897
wikiData Q105328118