Asperiene A

Details

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Internal ID f46e5a7b-f4da-4b58-8077-6e298311b2ae
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name [(5R,5aS,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-1-oxo-3,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-5-yl] (6R,7R)-6,7-dihydroxyocta-2,4-dienoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H32O7/c1-14(24)16(25)8-5-6-9-18(26)30-17-12-15-13-29-20(27)23(15,28)22(4)11-7-10-21(2,3)19(17)22/h5-6,8-9,12,14,16-17,19,24-25,28H,7,10-11,13H2,1-4H3/t14-,16-,17-,19+,22+,23+/m1/s1
InChI Key AVBLSPPEZPLINV-AACNEDLZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H32O7
Molecular Weight 420.50 g/mol
Exact Mass 420.21480336 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.81
H-Bond Acceptor 7
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 Asperiene A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9771 97.71%
Caco-2 - 0.6699 66.99%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.8692 86.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8559 85.59%
OATP1B3 inhibitior + 0.8342 83.42%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6032 60.32%
BSEP inhibitior - 0.7421 74.21%
P-glycoprotein inhibitior - 0.5600 56.00%
P-glycoprotein substrate - 0.6377 63.77%
CYP3A4 substrate + 0.6654 66.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9037 90.37%
CYP3A4 inhibition - 0.8399 83.99%
CYP2C9 inhibition - 0.5206 52.06%
CYP2C19 inhibition - 0.8123 81.23%
CYP2D6 inhibition - 0.9072 90.72%
CYP1A2 inhibition - 0.5080 50.80%
CYP2C8 inhibition - 0.5811 58.11%
CYP inhibitory promiscuity - 0.8205 82.05%
UGT catelyzed - 0.6638 66.38%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5082 50.82%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.9656 96.56%
Skin irritation - 0.5317 53.17%
Skin corrosion - 0.9249 92.49%
Ames mutagenesis - 0.6154 61.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4922 49.22%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.6626 66.26%
skin sensitisation - 0.8256 82.56%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.6390 63.90%
Acute Oral Toxicity (c) III 0.5314 53.14%
Estrogen receptor binding + 0.6732 67.32%
Androgen receptor binding + 0.6495 64.95%
Thyroid receptor binding + 0.6330 63.30%
Glucocorticoid receptor binding + 0.6742 67.42%
Aromatase binding + 0.6420 64.20%
PPAR gamma - 0.6286 62.86%
Honey bee toxicity - 0.8093 80.93%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9957 99.57%

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 94.80% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.03% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.02% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.93% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.39% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.33% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.09% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.28% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.73% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 84.96% 94.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.88% 96.77%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.76% 95.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.17% 97.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.00% 97.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.80% 91.07%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.17% 100.00%

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 146683068
LOTUS LTS0244748
wikiData Q104919308