Coriandrin

Details

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Internal ID 9f28ff1b-5241-4797-ba6e-926826b9a684
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 4-methoxy-7-methylfuro[2,3-g]isochromen-5-one
SMILES (Canonical) CC1=CC2=CC3=C(C=CO3)C(=C2C(=O)O1)OC
SMILES (Isomeric) CC1=CC2=CC3=C(C=CO3)C(=C2C(=O)O1)OC
InChI InChI=1S/C13H10O4/c1-7-5-8-6-10-9(3-4-16-10)12(15-2)11(8)13(14)17-7/h3-6H,1-2H3
InChI Key BUZQIMYNOWPYHH-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10O4
Molecular Weight 230.22 g/mol
Exact Mass 230.05790880 g/mol
Topological Polar Surface Area (TPSA) 48.70 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.86
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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116408-80-1
4-methoxy-7-methylfuro[2,3-g]isochromen-5-one
4-Methoxy-7-methyl-5H-furo(2,3-g)benzopyran-5-one
CCRIS 8086
CARIANDRIN
DTXSID00151389
CHEBI:174178
AKOS040736239
4-methoxy-7-methyluro[2,3-g]isochromen-5-one
Q1132748
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Coriandrin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 + 0.8346 83.46%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6443 64.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9592 95.92%
OATP1B3 inhibitior - 0.2310 23.10%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7913 79.13%
P-glycoprotein inhibitior - 0.8085 80.85%
P-glycoprotein substrate - 0.8980 89.80%
CYP3A4 substrate - 0.5123 51.23%
CYP2C9 substrate - 0.6417 64.17%
CYP2D6 substrate - 0.8725 87.25%
CYP3A4 inhibition + 0.7999 79.99%
CYP2C9 inhibition + 0.6615 66.15%
CYP2C19 inhibition + 0.8845 88.45%
CYP2D6 inhibition + 0.9005 90.05%
CYP1A2 inhibition + 0.9546 95.46%
CYP2C8 inhibition - 0.7884 78.84%
CYP inhibitory promiscuity + 0.7613 76.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.3692 36.92%
Eye corrosion - 0.8997 89.97%
Eye irritation + 0.7106 71.06%
Skin irritation - 0.6777 67.77%
Skin corrosion - 0.9843 98.43%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3848 38.48%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8585 85.85%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.8244 82.44%
Acute Oral Toxicity (c) III 0.6520 65.20%
Estrogen receptor binding + 0.7834 78.34%
Androgen receptor binding + 0.7902 79.02%
Thyroid receptor binding - 0.5149 51.49%
Glucocorticoid receptor binding + 0.6135 61.35%
Aromatase binding + 0.8452 84.52%
PPAR gamma + 0.7311 73.11%
Honey bee toxicity - 0.8687 86.87%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9002 90.02%

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
CHEMBL1951 P21397 Monoamine oxidase A 94.38% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.08% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.14% 94.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 92.37% 93.65%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.29% 95.56%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 92.18% 94.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.79% 86.33%
CHEMBL2581 P07339 Cathepsin D 85.59% 98.95%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.40% 96.67%
CHEMBL3401 O75469 Pregnane X receptor 85.22% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.97% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.52% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.47% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.18% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.37% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.18% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.79% 99.17%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.39% 94.42%
CHEMBL2535 P11166 Glucose transporter 80.30% 98.75%

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.
Coriandrum sativum

Cross-Links

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PubChem 119586
LOTUS LTS0109904
wikiData Q1132748