Exserolide D

Details

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Internal ID 9e53a056-19ac-4f17-b30e-6afcf9303019
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives
IUPAC Name (2S,3aR,9bR)-6,8-dihydroxy-7-methoxy-2-propyl-2,3,3a,9b-tetrahydrofuro[3,2-c]isochromen-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H18O6/c1-3-4-7-5-10-13(20-7)8-6-9(16)14(19-2)12(17)11(8)15(18)21-10/h6-7,10,13,16-17H,3-5H2,1-2H3/t7-,10+,13+/m0/s1
InChI Key ZXWQOPCWRZRWHP-JVQVWZCXSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O6
Molecular Weight 294.30 g/mol
Exact Mass 294.11033829 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Exserolide D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9025 90.25%
Caco-2 + 0.7048 70.48%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6954 69.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8532 85.32%
OATP1B3 inhibitior + 0.8432 84.32%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9400 94.00%
P-glycoprotein inhibitior - 0.8287 82.87%
P-glycoprotein substrate - 0.7957 79.57%
CYP3A4 substrate + 0.5511 55.11%
CYP2C9 substrate + 0.6290 62.90%
CYP2D6 substrate - 0.8305 83.05%
CYP3A4 inhibition - 0.6028 60.28%
CYP2C9 inhibition - 0.6718 67.18%
CYP2C19 inhibition - 0.5183 51.83%
CYP2D6 inhibition - 0.7425 74.25%
CYP1A2 inhibition + 0.5138 51.38%
CYP2C8 inhibition - 0.6027 60.27%
CYP inhibitory promiscuity + 0.6124 61.24%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5276 52.76%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.7987 79.87%
Skin irritation - 0.7816 78.16%
Skin corrosion - 0.9339 93.39%
Ames mutagenesis - 0.5824 58.24%
Human Ether-a-go-go-Related Gene inhibition - 0.4673 46.73%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.5838 58.38%
skin sensitisation - 0.7806 78.06%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.4739 47.39%
Acute Oral Toxicity (c) III 0.4534 45.34%
Estrogen receptor binding + 0.7531 75.31%
Androgen receptor binding - 0.5115 51.15%
Thyroid receptor binding + 0.6298 62.98%
Glucocorticoid receptor binding + 0.8302 83.02%
Aromatase binding - 0.6556 65.56%
PPAR gamma + 0.5473 54.73%
Honey bee toxicity - 0.9156 91.56%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5232 52.32%
Fish aquatic toxicity + 0.9228 92.28%

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 99.24% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.03% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.82% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.05% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.76% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.20% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.56% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.57% 92.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.52% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.24% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.60% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 85.09% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.75% 95.56%
CHEMBL4208 P20618 Proteasome component C5 82.91% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.18% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.11% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.52% 89.00%

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 101904856
LOTUS LTS0110536
wikiData Q75067424