(-)-Columbianetin

Details

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Internal ID 6d4cb858-aac5-4134-8812-339378732620
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Furanocoumarins > Angular furanocoumarins
IUPAC Name (8R)-8-(2-hydroxypropan-2-yl)-8,9-dihydrofuro[2,3-h]chromen-2-one
SMILES (Canonical) CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O
SMILES (Isomeric) CC(C)([C@H]1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O
InChI InChI=1S/C14H14O4/c1-14(2,16)11-7-9-10(17-11)5-3-8-4-6-12(15)18-13(8)9/h3-6,11,16H,7H2,1-2H3/t11-/m1/s1
InChI Key YRAQEMCYCSSHJG-LLVKDONJSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O4
Molecular Weight 246.26 g/mol
Exact Mass 246.08920892 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.87
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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(-)-columbianetin
52842-47-4
Columbianetin
(8R)-8-(2-hydroxypropan-2-yl)-8,9-dihydro-2H-furo[2,3-h]chromen-2-one
(8R)-8,9-dihydro-8-(1-hydroxy-1-methylethyl)-2H-furo[2,3-h]1-benzopyran-2-one
CHEBI:3828
SCHEMBL21527679
DTXSID30331738
C09210
Q27106206
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (-)-Columbianetin

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 - 0.7329 73.29%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7949 79.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9450 94.50%
OATP1B3 inhibitior + 0.8861 88.61%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7866 78.66%
P-glycoprotein inhibitior - 0.8901 89.01%
P-glycoprotein substrate - 0.9329 93.29%
CYP3A4 substrate - 0.5782 57.82%
CYP2C9 substrate - 0.6506 65.06%
CYP2D6 substrate - 0.8062 80.62%
CYP3A4 inhibition - 0.8285 82.85%
CYP2C9 inhibition - 0.7486 74.86%
CYP2C19 inhibition - 0.7313 73.13%
CYP2D6 inhibition - 0.8270 82.70%
CYP1A2 inhibition - 0.6717 67.17%
CYP2C8 inhibition - 0.8625 86.25%
CYP inhibitory promiscuity - 0.9103 91.03%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5086 50.86%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.7424 74.24%
Skin irritation - 0.6980 69.80%
Skin corrosion - 0.9226 92.26%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6129 61.29%
Micronuclear + 0.5259 52.59%
Hepatotoxicity + 0.6533 65.33%
skin sensitisation - 0.7374 73.74%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.4610 46.10%
Acute Oral Toxicity (c) III 0.5836 58.36%
Estrogen receptor binding + 0.7093 70.93%
Androgen receptor binding + 0.5586 55.86%
Thyroid receptor binding - 0.6064 60.64%
Glucocorticoid receptor binding - 0.5670 56.70%
Aromatase binding + 0.6193 61.93%
PPAR gamma + 0.7668 76.68%
Honey bee toxicity - 0.9474 94.74%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9463 94.63%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.11% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.52% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.08% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.42% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.66% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 86.64% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.84% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.06% 94.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.81% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.41% 85.14%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.54% 93.04%

Cross-Links

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PubChem 442104
NPASS NPC201581
LOTUS LTS0097915
wikiData Q27106206