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(1S,3S,9R,11S)-7-(3,4-dihydroxybenzoyl)-11-[(2S)-2,3-dihydroxy-3-methylbutyl]-4,4,10,10-tetramethyl-3,9-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione

Table of Contents

Details
Physical and Chemical Properties
Synonyms
2D Structure
3D Structure
ADMET Properties
Targets (proven and/or predicted)
Plants that contains it
Cross-Links

Details

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Internal ID f306f46a-1957-45a9-9edc-6129662a904e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name (1S,3S,9R,11S)-7-(3,4-dihydroxybenzoyl)-11-[(2S)-2,3-dihydroxy-3-methylbutyl]-4,4,10,10-tetramethyl-3,9-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione
SMILES (Canonical) CC(=CCC1CC23CC(C(C(C2=O)(C(=O)C(=C3OC1(C)C)C(=O)C4=CC(=C(C=C4)O)O)CC=C(C)C)(C)C)CC(C(C)(C)O)O)C
SMILES (Isomeric) CC(=CC[C@H]1C[C@]23C[C@H](C([C@](C2=O)(C(=O)C(=C3OC1(C)C)C(=O)C4=CC(=C(C=C4)O)O)CC=C(C)C)(C)C)C[C@@H](C(C)(C)O)O)C
InChI InChI=1S/C38H52O8/c1-21(2)11-13-24-19-37-20-25(18-28(41)35(7,8)45)34(5,6)38(33(37)44,16-15-22(3)4)31(43)29(32(37)46-36(24,9)10)30(42)23-12-14-26(39)27(40)17-23/h11-12,14-15,17,24-25,28,39-41,45H,13,16,18-20H2,1-10H3/t24-,25+,28-,37+,38-/m0/s1
InChI Key LSEYPIXFPUCVGX-MPBJXSSYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C38H52O8
Molecular Weight 636.80 g/mol
Exact Mass 636.36621861 g/mol
Topological Polar Surface Area (TPSA) 141.00 Ų
XlogP 6.60
Atomic LogP (AlogP) 6.75
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,3S,9R,11S)-7-(3,4-dihydroxybenzoyl)-11-[(2S)-2,3-dihydroxy-3-methylbutyl]-4,4,10,10-tetramethyl-3,9-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9863 98.63%
Caco-2 - 0.7886 78.86%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7351 73.51%
OATP2B1 inhibitior - 0.5671 56.71%
OATP1B1 inhibitior + 0.8734 87.34%
OATP1B3 inhibitior + 0.9476 94.76%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9826 98.26%
P-glycoprotein inhibitior + 0.7362 73.62%
P-glycoprotein substrate + 0.6437 64.37%
CYP3A4 substrate + 0.6789 67.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8257 82.57%
CYP3A4 inhibition - 0.8939 89.39%
CYP2C9 inhibition + 0.5124 51.24%
CYP2C19 inhibition + 0.5616 56.16%
CYP2D6 inhibition - 0.7822 78.22%
CYP1A2 inhibition - 0.5549 55.49%
CYP2C8 inhibition + 0.6953 69.53%
CYP inhibitory promiscuity - 0.8020 80.20%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6628 66.28%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.8958 89.58%
Skin irritation - 0.6620 66.20%
Skin corrosion - 0.9067 90.67%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3601 36.01%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.5248 52.48%
skin sensitisation - 0.7196 71.96%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.4638 46.38%
Acute Oral Toxicity (c) III 0.4316 43.16%
Estrogen receptor binding + 0.7643 76.43%
Androgen receptor binding + 0.7608 76.08%
Thyroid receptor binding + 0.6390 63.90%
Glucocorticoid receptor binding + 0.8088 80.88%
Aromatase binding + 0.7504 75.04%
PPAR gamma + 0.6961 69.61%
Honey bee toxicity - 0.7959 79.59%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9864 98.64%

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 99.39% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.04% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.34% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.80% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 93.56% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 93.01% 94.73%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 92.07% 93.40%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.81% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 89.55% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.77% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.12% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.74% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.85% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.76% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.23% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.67% 90.71%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.60% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.43% 99.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.16% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.15% 89.34%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.07% 97.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.01% 97.09%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.60% 96.90%

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.
Moronobea coccinea

Cross-Links

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PubChem 102283883
LOTUS LTS0168678
wikiData Q104400391