(3aR,5aS,8R,8aR,9aR)-5,8-dimethyl-1-methylidene-8-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-5a,6,7,8a,9,9a-hexahydro-3aH-azuleno[6,5-b]furan-2-one

Details

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Internal ID b5a0aa53-a29a-4238-abfa-3852f3f4adce
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Guaianolides and derivatives
IUPAC Name (3aR,5aS,8R,8aR,9aR)-5,8-dimethyl-1-methylidene-8-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-5a,6,7,8a,9,9a-hexahydro-3aH-azuleno[6,5-b]furan-2-one
SMILES (Canonical) CC1C(C(C(C(O1)OC2(CCC3C2CC4C(C=C3C)OC(=O)C4=C)C)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@]2(CC[C@H]3[C@H]2C[C@H]4[C@@H](C=C3C)OC(=O)C4=C)C)O)O)O
InChI InChI=1S/C21H30O7/c1-9-7-15-13(10(2)19(25)27-15)8-14-12(9)5-6-21(14,4)28-20-18(24)17(23)16(22)11(3)26-20/h7,11-18,20,22-24H,2,5-6,8H2,1,3-4H3/t11-,12+,13+,14+,15+,16-,17+,18+,20-,21+/m0/s1
InChI Key XUPDHFIEIOXDJS-SPCYKQKYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H30O7
Molecular Weight 394.50 g/mol
Exact Mass 394.19915329 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.06
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3aR,5aS,8R,8aR,9aR)-5,8-dimethyl-1-methylidene-8-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-5a,6,7,8a,9,9a-hexahydro-3aH-azuleno[6,5-b]furan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8830 88.30%
Caco-2 - 0.6579 65.79%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6339 63.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8259 82.59%
OATP1B3 inhibitior + 0.9043 90.43%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8310 83.10%
P-glycoprotein inhibitior - 0.7860 78.60%
P-glycoprotein substrate - 0.7886 78.86%
CYP3A4 substrate + 0.6749 67.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8740 87.40%
CYP3A4 inhibition - 0.8304 83.04%
CYP2C9 inhibition - 0.8653 86.53%
CYP2C19 inhibition - 0.8362 83.62%
CYP2D6 inhibition - 0.9392 93.92%
CYP1A2 inhibition - 0.5893 58.93%
CYP2C8 inhibition + 0.4873 48.73%
CYP inhibitory promiscuity - 0.9441 94.41%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5950 59.50%
Eye corrosion - 0.9865 98.65%
Eye irritation - 0.9689 96.89%
Skin irritation - 0.5182 51.82%
Skin corrosion - 0.9044 90.44%
Ames mutagenesis - 0.7354 73.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5273 52.73%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8004 80.04%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.8675 86.75%
Acute Oral Toxicity (c) III 0.3289 32.89%
Estrogen receptor binding + 0.7249 72.49%
Androgen receptor binding + 0.5884 58.84%
Thyroid receptor binding + 0.6995 69.95%
Glucocorticoid receptor binding + 0.6324 63.24%
Aromatase binding - 0.4846 48.46%
PPAR gamma + 0.5229 52.29%
Honey bee toxicity - 0.7031 70.31%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9804 98.04%

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
CHEMBL3714130 P46095 G-protein coupled receptor 6 95.44% 97.36%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.57% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.23% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.08% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.07% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.29% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.34% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 87.63% 94.75%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.54% 97.25%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 86.52% 97.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.30% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.64% 96.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.06% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.08% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.93% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.89% 93.03%
CHEMBL221 P23219 Cyclooxygenase-1 81.12% 90.17%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.04% 82.38%

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.
Helenium radiatum

Cross-Links

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PubChem 162925044
LOTUS LTS0241034
wikiData Q105342478