Solistatinol

Details

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Internal ID dd947b12-350e-410b-aa0b-1c15156c66f5
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name (4R,6R)-4-hydroxy-6-[2-(8-hydroxy-2-methylnaphthalen-1-yl)ethyl]oxan-2-one
SMILES (Canonical) CC1=C(C2=C(C=CC=C2O)C=C1)CCC3CC(CC(=O)O3)O
SMILES (Isomeric) CC1=C(C2=C(C=CC=C2O)C=C1)CC[C@@H]3C[C@H](CC(=O)O3)O
InChI InChI=1S/C18H20O4/c1-11-5-6-12-3-2-4-16(20)18(12)15(11)8-7-14-9-13(19)10-17(21)22-14/h2-6,13-14,19-20H,7-10H2,1H3/t13-,14-/m1/s1
InChI Key WPIRBMJVHYVQRJ-ZIAGYGMSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H20O4
Molecular Weight 300.30 g/mol
Exact Mass 300.13615911 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 4
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 Solistatinol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9484 94.84%
Caco-2 + 0.7091 70.91%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7226 72.26%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.8741 87.41%
OATP1B3 inhibitior + 0.9487 94.87%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7768 77.68%
P-glycoprotein inhibitior - 0.6906 69.06%
P-glycoprotein substrate - 0.6777 67.77%
CYP3A4 substrate + 0.5345 53.45%
CYP2C9 substrate - 0.7891 78.91%
CYP2D6 substrate - 0.7474 74.74%
CYP3A4 inhibition - 0.6134 61.34%
CYP2C9 inhibition - 0.8753 87.53%
CYP2C19 inhibition - 0.7701 77.01%
CYP2D6 inhibition - 0.8941 89.41%
CYP1A2 inhibition + 0.5132 51.32%
CYP2C8 inhibition + 0.5180 51.80%
CYP inhibitory promiscuity - 0.8600 86.00%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6897 68.97%
Eye corrosion - 0.9941 99.41%
Eye irritation - 0.8157 81.57%
Skin irritation - 0.6389 63.89%
Skin corrosion - 0.9314 93.14%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6443 64.43%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5639 56.39%
skin sensitisation - 0.8802 88.02%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.4513 45.13%
Acute Oral Toxicity (c) III 0.3584 35.84%
Estrogen receptor binding + 0.9110 91.10%
Androgen receptor binding + 0.6891 68.91%
Thyroid receptor binding - 0.5751 57.51%
Glucocorticoid receptor binding - 0.5141 51.41%
Aromatase binding + 0.5886 58.86%
PPAR gamma + 0.8047 80.47%
Honey bee toxicity - 0.9141 91.41%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9800 98.00%

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
CHEMBL230 P35354 Cyclooxygenase-2 95.96% 89.63%
CHEMBL2996 Q05655 Protein kinase C delta 95.65% 97.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.73% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.01% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.76% 97.09%
CHEMBL2581 P07339 Cathepsin D 92.68% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.69% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.64% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 89.51% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.13% 96.95%
CHEMBL240 Q12809 HERG 87.08% 89.76%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.19% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 85.40% 91.49%
CHEMBL220 P22303 Acetylcholinesterase 83.26% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.02% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 81.71% 93.31%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.41% 93.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.05% 93.03%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.76% 93.99%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 80.22% 96.39%

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 102154716
LOTUS LTS0019001
wikiData Q77502889