[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-pent-2-enoate

Details

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Internal ID 3313a0fc-0e45-4859-a37a-eae2be2cd198
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Rhamnofolane and daphnane diterpenoids
IUPAC Name [(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-pent-2-enoate
SMILES (Canonical) CCC=CC(=O)OC1C(C23C4C=C(C(=O)C4(C(C5(C(C2C6C1(OC(O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C
SMILES (Isomeric) CC/C=C/C(=O)O[C@@H]1[C@H]([C@]23[C@@H]4C=C(C(=O)[C@]4([C@@H]([C@@]5([C@H]([C@H]2[C@@H]6[C@]1(O[C@@](O6)(O3)C7=CC=CC=C7)C(=C)C)O5)CO)O)O)C)C
InChI InChI=1S/C32H36O10/c1-6-7-13-21(34)38-24-18(5)31-20-14-17(4)23(35)29(20,37)27(36)28(15-33)25(39-28)22(31)26-30(24,16(2)3)41-32(40-26,42-31)19-11-9-8-10-12-19/h7-14,18,20,22,24-27,33,36-37H,2,6,15H2,1,3-5H3/b13-7+/t18-,20-,22+,24-,25+,26-,27-,28+,29-,30+,31+,32-/m1/s1
InChI Key GMGZRLUWSNMNKB-NEGGUVPJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H36O10
Molecular Weight 580.60 g/mol
Exact Mass 580.23084734 g/mol
Topological Polar Surface Area (TPSA) 144.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.82
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,2R,6S,7S,8R,10S,11S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-14-phenyl-16-prop-1-en-2-yl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] (E)-pent-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8638 86.38%
Caco-2 - 0.8094 80.94%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6847 68.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8212 82.12%
OATP1B3 inhibitior + 0.9158 91.58%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9535 95.35%
P-glycoprotein inhibitior + 0.7587 75.87%
P-glycoprotein substrate + 0.5557 55.57%
CYP3A4 substrate + 0.6869 68.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8773 87.73%
CYP3A4 inhibition - 0.5134 51.34%
CYP2C9 inhibition - 0.7538 75.38%
CYP2C19 inhibition - 0.7488 74.88%
CYP2D6 inhibition - 0.9135 91.35%
CYP1A2 inhibition - 0.8096 80.96%
CYP2C8 inhibition + 0.7083 70.83%
CYP inhibitory promiscuity - 0.5706 57.06%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6194 61.94%
Eye corrosion - 0.9825 98.25%
Eye irritation - 0.8978 89.78%
Skin irritation - 0.7380 73.80%
Skin corrosion - 0.9279 92.79%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3745 37.45%
Micronuclear - 0.5041 50.41%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8113 81.13%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5894 58.94%
Acute Oral Toxicity (c) III 0.4866 48.66%
Estrogen receptor binding + 0.7612 76.12%
Androgen receptor binding + 0.7286 72.86%
Thyroid receptor binding + 0.6458 64.58%
Glucocorticoid receptor binding + 0.6932 69.32%
Aromatase binding + 0.6652 66.52%
PPAR gamma + 0.6658 66.58%
Honey bee toxicity - 0.7805 78.05%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9755 97.55%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.31% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.60% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.91% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.12% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.65% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 94.13% 94.62%
CHEMBL2581 P07339 Cathepsin D 93.89% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.62% 95.56%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.83% 94.08%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.89% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 85.56% 90.17%
CHEMBL5028 O14672 ADAM10 81.49% 97.50%
CHEMBL3401 O75469 Pregnane X receptor 81.31% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.70% 89.00%

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.
Thymelaea hirsuta

Cross-Links

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PubChem 163012668
LOTUS LTS0143170
wikiData Q105011814