Columbianetin acetate

Details

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Internal ID 92188702-60e6-4377-a3ca-e167de0ec820
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Furanocoumarins > Angular furanocoumarins
IUPAC Name 2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl acetate
SMILES (Canonical) CC(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3
SMILES (Isomeric) CC(=O)OC(C)(C)[C@@H]1CC2=C(O1)C=CC3=C2OC(=O)C=C3
InChI InChI=1S/C16H16O5/c1-9(17)21-16(2,3)13-8-11-12(19-13)6-4-10-5-7-14(18)20-15(10)11/h4-7,13H,8H2,1-3H3/t13-/m0/s1
InChI Key IQTTZQQJJBEAIM-ZDUSSCGKSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O5
Molecular Weight 288.29 g/mol
Exact Mass 288.09977361 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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23180-65-6
O-Acetylcolumbianetin
(+)-Columbianetin acetate
2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl acetate
(S)-Columbianetin acetate
Acetyl columbianetin
(8S)-columbianetin acetate
(8S)-O-acetylcolumbianetin
SCHEMBL12247775
HY-N0363A
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 acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 - 0.9372 93.72%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7038 70.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9579 95.79%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6076 60.76%
P-glycoprotein inhibitior - 0.5826 58.26%
P-glycoprotein substrate - 0.9016 90.16%
CYP3A4 substrate - 0.5211 52.11%
CYP2C9 substrate - 0.8149 81.49%
CYP2D6 substrate - 0.8380 83.80%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.8291 82.91%
CYP2C19 inhibition - 0.6258 62.58%
CYP2D6 inhibition - 0.8338 83.38%
CYP1A2 inhibition - 0.6663 66.63%
CYP2C8 inhibition - 0.8601 86.01%
CYP inhibitory promiscuity - 0.7472 74.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4547 45.47%
Eye corrosion - 0.9845 98.45%
Eye irritation - 0.9388 93.88%
Skin irritation - 0.8024 80.24%
Skin corrosion - 0.9341 93.41%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8357 83.57%
Micronuclear - 0.5341 53.41%
Hepatotoxicity + 0.5408 54.08%
skin sensitisation - 0.7553 75.53%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.4739 47.39%
Acute Oral Toxicity (c) III 0.6428 64.28%
Estrogen receptor binding + 0.8682 86.82%
Androgen receptor binding + 0.6466 64.66%
Thyroid receptor binding - 0.6312 63.12%
Glucocorticoid receptor binding + 0.5370 53.70%
Aromatase binding + 0.7700 77.00%
PPAR gamma - 0.5823 58.23%
Honey bee toxicity - 0.9209 92.09%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9757 97.57%

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
CHEMBL2581 P07339 Cathepsin D 92.26% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.70% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.64% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.41% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.39% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.17% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.72% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 81.13% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.26% 86.33%

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.
Angelica pubescens
Aralia continentalis
Cnidium monnieri
Hansenia forbesii
Hansenia weberbaueriana
Murraya koenigii
Seseli schrenkianum
Tordylium apulum
Torilis japonica

Cross-Links

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PubChem 161409
NPASS NPC296115
LOTUS LTS0021879
wikiData Q72461280