Isoguamarol

Details

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Internal ID a63e1741-df42-4db0-90ce-cc91adff1313
Taxonomy Lignans, neolignans and related compounds > Furanoid lignans > Tetrahydrofuran lignans > 9,9-epoxylignans > Dibenzylbutyrolactone lignans
IUPAC Name (3Z,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3-hydroxy-4-methoxyphenyl)methylidene]oxolan-2-one
SMILES (Canonical) COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)O
SMILES (Isomeric) COC1=C(C=C(C=C1)/C=C\2/[C@H](COC2=O)CC3=CC4=C(C=C3)OCO4)O
InChI InChI=1S/C20H18O6/c1-23-17-4-2-13(8-16(17)21)7-15-14(10-24-20(15)22)6-12-3-5-18-19(9-12)26-11-25-18/h2-5,7-9,14,21H,6,10-11H2,1H3/b15-7-/t14-/m0/s1
InChI Key RDQYZETVAPDYFY-FQNPWXFGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O6
Molecular Weight 354.40 g/mol
Exact Mass 354.11033829 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.93
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Isoguamarol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.6739 67.39%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8093 80.93%
OATP2B1 inhibitior - 0.8618 86.18%
OATP1B1 inhibitior + 0.9208 92.08%
OATP1B3 inhibitior + 0.9673 96.73%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9219 92.19%
P-glycoprotein inhibitior + 0.7819 78.19%
P-glycoprotein substrate - 0.7589 75.89%
CYP3A4 substrate + 0.5814 58.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7969 79.69%
CYP3A4 inhibition + 0.8876 88.76%
CYP2C9 inhibition + 0.9332 93.32%
CYP2C19 inhibition + 0.9362 93.62%
CYP2D6 inhibition + 0.7075 70.75%
CYP1A2 inhibition + 0.6034 60.34%
CYP2C8 inhibition + 0.5256 52.56%
CYP inhibitory promiscuity + 0.9431 94.31%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Danger 0.4060 40.60%
Eye corrosion - 0.9838 98.38%
Eye irritation - 0.7523 75.23%
Skin irritation - 0.7362 73.62%
Skin corrosion - 0.9485 94.85%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6554 65.54%
Micronuclear + 0.7474 74.74%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.5616 56.16%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6370 63.70%
Acute Oral Toxicity (c) III 0.5996 59.96%
Estrogen receptor binding + 0.9094 90.94%
Androgen receptor binding + 0.6412 64.12%
Thyroid receptor binding + 0.5899 58.99%
Glucocorticoid receptor binding + 0.6975 69.75%
Aromatase binding + 0.6076 60.76%
PPAR gamma + 0.7959 79.59%
Honey bee toxicity - 0.8234 82.34%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9821 98.21%

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 98.29% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.78% 94.45%
CHEMBL2581 P07339 Cathepsin D 96.88% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.02% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 95.44% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.98% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 93.84% 92.62%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.37% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.11% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.32% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.93% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.08% 95.50%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.76% 96.77%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.64% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.61% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.57% 99.17%
CHEMBL2535 P11166 Glucose transporter 87.40% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.69% 96.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.16% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.50% 94.00%

Cross-Links

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PubChem 101630409
NPASS NPC94966
LOTUS LTS0049318
wikiData Q104402323