Spirodalesol

Details

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Internal ID c84451d5-1bf1-48f9-9814-ef8d752fddd6
Taxonomy Lignans, neolignans and related compounds > Aryltetralin lignans
IUPAC Name methyl 5,7',15'-trihydroxy-4,9',17'-trioxospiro[naphthalene-1,11'-pentacyclo[10.7.1.02,10.03,8.016,20]icosa-1,3(8),4,6,12(20),13,15,18-octaene]-10'-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H18O8/c1-39-29(38)31-27(14-4-2-6-18(32)24(14)28(31)37)15-8-10-20(34)26-21(35)11-9-17(23(15)26)30(31)13-12-22(36)25-16(30)5-3-7-19(25)33/h2-13,32-33,35H,1H3
InChI Key MGLQXZJRIOSKCO-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C31H18O8
Molecular Weight 518.50 g/mol
Exact Mass 518.10016753 g/mol
Topological Polar Surface Area (TPSA) 138.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 3.87
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Spirodalesol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 - 0.6520 65.20%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8665 86.65%
OATP2B1 inhibitior - 0.7105 71.05%
OATP1B1 inhibitior + 0.9084 90.84%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7844 78.44%
P-glycoprotein inhibitior - 0.5405 54.05%
P-glycoprotein substrate + 0.5534 55.34%
CYP3A4 substrate + 0.6668 66.68%
CYP2C9 substrate - 0.8070 80.70%
CYP2D6 substrate - 0.8770 87.70%
CYP3A4 inhibition - 0.8766 87.66%
CYP2C9 inhibition + 0.7557 75.57%
CYP2C19 inhibition - 0.5839 58.39%
CYP2D6 inhibition - 0.8738 87.38%
CYP1A2 inhibition + 0.6524 65.24%
CYP2C8 inhibition + 0.6082 60.82%
CYP inhibitory promiscuity + 0.5439 54.39%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8287 82.87%
Carcinogenicity (trinary) Danger 0.4241 42.41%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.5095 50.95%
Skin irritation - 0.6225 62.25%
Skin corrosion - 0.9470 94.70%
Ames mutagenesis + 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7082 70.82%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8127 81.27%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.7518 75.18%
Acute Oral Toxicity (c) III 0.4028 40.28%
Estrogen receptor binding + 0.7547 75.47%
Androgen receptor binding + 0.6606 66.06%
Thyroid receptor binding - 0.5850 58.50%
Glucocorticoid receptor binding + 0.6728 67.28%
Aromatase binding - 0.5977 59.77%
PPAR gamma + 0.7634 76.34%
Honey bee toxicity - 0.8968 89.68%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9973 99.73%

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 98.65% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.00% 91.49%
CHEMBL2581 P07339 Cathepsin D 96.36% 98.95%
CHEMBL4208 P20618 Proteasome component C5 93.75% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.39% 95.56%
CHEMBL3492 P49721 Proteasome Macropain subunit 90.71% 90.24%
CHEMBL2535 P11166 Glucose transporter 90.41% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.13% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.89% 96.09%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.28% 96.67%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.17% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.87% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.42% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.63% 95.50%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.43% 92.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.91% 99.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.61% 82.69%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.35% 93.03%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.35% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.25% 89.00%

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.
There are no matching plants.

Cross-Links

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PubChem 132584550
LOTUS LTS0269098
wikiData Q105163420