Isoasteltoxin

Details

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Internal ID c0c88a76-6cbd-4882-96be-91d2ca7ec5e4
Taxonomy Organoheterocyclic compounds > Furofurans
IUPAC Name 6-[(1Z,3Z,5E)-6-[(2R,3R,3aR,4R,5R,6aS)-2-ethyl-3,4-dihydroxy-3,3a-dimethyl-2,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl]hexa-1,3,5-trienyl]-4-methoxy-5-methylpyran-2-one
SMILES (Canonical) CCC1C(C2(C(C(OC2O1)C=CC=CC=CC3=C(C(=CC(=O)O3)OC)C)O)C)(C)O
SMILES (Isomeric) CC[C@@H]1[C@]([C@]2([C@H]([C@H](O[C@H]2O1)/C=C/C=C\C=C/C3=C(C(=CC(=O)O3)OC)C)O)C)(C)O
InChI InChI=1S/C23H30O7/c1-6-18-23(4,26)22(3)20(25)16(29-21(22)30-18)12-10-8-7-9-11-15-14(2)17(27-5)13-19(24)28-15/h7-13,16,18,20-21,25-26H,6H2,1-5H3/b8-7-,11-9-,12-10+/t16-,18-,20+,21+,22+,23+/m1/s1
InChI Key GPXPJKFETRLRAS-USSSIYHESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H30O7
Molecular Weight 418.50 g/mol
Exact Mass 418.19915329 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Isoasteltoxin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9685 96.85%
Caco-2 - 0.6368 63.68%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5586 55.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8579 85.79%
OATP1B3 inhibitior + 0.8038 80.38%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8618 86.18%
P-glycoprotein inhibitior + 0.6456 64.56%
P-glycoprotein substrate - 0.5190 51.90%
CYP3A4 substrate + 0.6272 62.72%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8580 85.80%
CYP3A4 inhibition - 0.8122 81.22%
CYP2C9 inhibition - 0.8456 84.56%
CYP2C19 inhibition - 0.7672 76.72%
CYP2D6 inhibition - 0.9168 91.68%
CYP1A2 inhibition - 0.7468 74.68%
CYP2C8 inhibition + 0.5934 59.34%
CYP inhibitory promiscuity - 0.6524 65.24%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4784 47.84%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.9791 97.91%
Skin irritation - 0.7263 72.63%
Skin corrosion - 0.9164 91.64%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8127 81.27%
Micronuclear - 0.5541 55.41%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7601 76.01%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.6333 63.33%
Acute Oral Toxicity (c) III 0.4045 40.45%
Estrogen receptor binding + 0.8507 85.07%
Androgen receptor binding + 0.6751 67.51%
Thyroid receptor binding + 0.7186 71.86%
Glucocorticoid receptor binding + 0.6452 64.52%
Aromatase binding + 0.7601 76.01%
PPAR gamma + 0.7303 73.03%
Honey bee toxicity - 0.8018 80.18%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5234 52.34%
Fish aquatic toxicity + 0.9036 90.36%

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 97.96% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.66% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.85% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.86% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 89.84% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.50% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.91% 94.00%
CHEMBL2581 P07339 Cathepsin D 85.36% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 85.26% 94.73%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.18% 92.94%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.44% 97.36%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.29% 91.71%
CHEMBL4208 P20618 Proteasome component C5 80.74% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.68% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.67% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.10% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139589588
LOTUS LTS0011178
wikiData Q105015230