(1R,3R,8R,18Z,20Z,24R,25S,26S)-17-(1-hydroxyethyl)-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,18,20-triene-26,2'-oxirane]-11,14,22-trione

Details

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Internal ID 8354bd46-7036-4de5-9819-08f4890d2e94
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Trichothecenes
IUPAC Name (1R,3R,8R,18Z,20Z,24R,25S,26S)-17-(1-hydroxyethyl)-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,18,20-triene-26,2'-oxirane]-11,14,22-trione
SMILES (Canonical) CC1CC(=O)OCC23CCC(=CC2OC4CC(C3(C45CO5)C)OC(=O)C=CC=CC(OCC1=O)C(C)O)C
SMILES (Isomeric) CC1CC(=O)OC[C@]23CCC(=C[C@H]2O[C@@H]4C[C@H]([C@]3([C@]45CO5)C)OC(=O)/C=C\C=C/C(OCC1=O)C(C)O)C
InChI InChI=1S/C29H38O9/c1-17-9-10-28-15-35-26(33)12-18(2)20(31)14-34-21(19(3)30)7-5-6-8-25(32)38-22-13-24(37-23(28)11-17)29(16-36-29)27(22,28)4/h5-8,11,18-19,21-24,30H,9-10,12-16H2,1-4H3/b7-5-,8-6-/t18?,19?,21?,22-,23-,24-,27-,28-,29+/m1/s1
InChI Key ARFRGJLJRXAOAX-AJNOSVGNSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C29H38O9
Molecular Weight 530.60 g/mol
Exact Mass 530.25158279 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,3R,8R,18Z,20Z,24R,25S,26S)-17-(1-hydroxyethyl)-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,18,20-triene-26,2'-oxirane]-11,14,22-trione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9193 91.93%
Caco-2 - 0.7369 73.69%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.7756 77.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8475 84.75%
OATP1B3 inhibitior + 0.9717 97.17%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6021 60.21%
BSEP inhibitior + 0.9759 97.59%
P-glycoprotein inhibitior + 0.8421 84.21%
P-glycoprotein substrate + 0.8655 86.55%
CYP3A4 substrate + 0.6901 69.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8942 89.42%
CYP3A4 inhibition - 0.9261 92.61%
CYP2C9 inhibition - 0.9063 90.63%
CYP2C19 inhibition - 0.9195 91.95%
CYP2D6 inhibition - 0.9497 94.97%
CYP1A2 inhibition - 0.7498 74.98%
CYP2C8 inhibition + 0.5172 51.72%
CYP inhibitory promiscuity - 0.9736 97.36%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5571 55.71%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9395 93.95%
Skin irritation - 0.5391 53.91%
Skin corrosion - 0.9217 92.17%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8126 81.26%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.6678 66.78%
skin sensitisation - 0.8508 85.08%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5614 56.14%
Acute Oral Toxicity (c) I 0.5627 56.27%
Estrogen receptor binding + 0.8674 86.74%
Androgen receptor binding + 0.7407 74.07%
Thyroid receptor binding + 0.5399 53.99%
Glucocorticoid receptor binding + 0.8609 86.09%
Aromatase binding + 0.7005 70.05%
PPAR gamma + 0.6123 61.23%
Honey bee toxicity - 0.5998 59.98%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9751 97.51%

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 97.40% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.45% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.36% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.11% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.00% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.71% 94.45%
CHEMBL2581 P07339 Cathepsin D 90.80% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.07% 100.00%
CHEMBL1951 P21397 Monoamine oxidase A 89.94% 91.49%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.76% 97.21%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.03% 99.23%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 87.71% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.46% 97.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.31% 96.47%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.12% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.67% 89.00%
CHEMBL4208 P20618 Proteasome component C5 84.68% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.70% 96.95%

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.
Baccharis megapotamica

Cross-Links

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PubChem 22524991
LOTUS LTS0116907
wikiData Q105099794