[(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)-but-2-enoate

Details

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Internal ID cc92fd1d-0f63-4552-814b-0361a14ba59f
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)-but-2-enoate
SMILES (Canonical) CC=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) C/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/C31H34O10/c1-6-10-20(33)37-23-17(5)30-19-13-16(4)22(34)28(19,36)26(35)27(14-32)24(38-27)21(30)25-29(23,15(2)3)40-31(39-25,41-30)18-11-8-7-9-12-18/h6-13,17,19,21,23-26,32,35-36H,2,14H2,1,3-5H3/b10-6+/t17-,19-,21+,23-,24+,25-,26-,27+,28-,29+,30+,31-/m1/s1
InChI Key SQTMWSJWSHZHCH-FCOWGZHTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H34O10
Molecular Weight 566.60 g/mol
Exact Mass 566.21519728 g/mol
Topological Polar Surface Area (TPSA) 144.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.43
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 5

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)-but-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 + 0.7983 79.83%
Caco-2 - 0.7911 79.11%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7105 71.05%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.8256 82.56%
OATP1B3 inhibitior + 0.9225 92.25%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9269 92.69%
P-glycoprotein inhibitior + 0.7474 74.74%
P-glycoprotein substrate + 0.5291 52.91%
CYP3A4 substrate + 0.6874 68.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8804 88.04%
CYP3A4 inhibition - 0.5848 58.48%
CYP2C9 inhibition - 0.7863 78.63%
CYP2C19 inhibition - 0.7722 77.22%
CYP2D6 inhibition - 0.9128 91.28%
CYP1A2 inhibition - 0.8338 83.38%
CYP2C8 inhibition + 0.6927 69.27%
CYP inhibitory promiscuity - 0.6317 63.17%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6235 62.35%
Eye corrosion - 0.9827 98.27%
Eye irritation - 0.8847 88.47%
Skin irritation - 0.7424 74.24%
Skin corrosion - 0.9297 92.97%
Ames mutagenesis - 0.7778 77.78%
Human Ether-a-go-go-Related Gene inhibition + 0.6992 69.92%
Micronuclear + 0.5059 50.59%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8099 80.99%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.7268 72.68%
Acute Oral Toxicity (c) III 0.4113 41.13%
Estrogen receptor binding + 0.7404 74.04%
Androgen receptor binding + 0.7275 72.75%
Thyroid receptor binding + 0.6464 64.64%
Glucocorticoid receptor binding + 0.6410 64.10%
Aromatase binding + 0.6345 63.45%
PPAR gamma + 0.6220 62.20%
Honey bee toxicity - 0.7645 76.45%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9680 96.80%

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 99.74% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.73% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 95.63% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.58% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.30% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.03% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.93% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.27% 98.95%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.46% 94.08%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.46% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 86.39% 94.73%
CHEMBL5028 O14672 ADAM10 82.68% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.75% 89.00%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 81.38% 94.23%

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 163191332
LOTUS LTS0272864
wikiData Q105258562