Citrusarin A

Details

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Internal ID 690c0e9c-c5db-43d9-8e4d-067cc2a3e416
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Pyranocoumarins > Angular pyranocoumarins
IUPAC Name 4,5,5,15,15-pentamethyl-3,8,14-trioxatetracyclo[11.4.0.02,6.07,12]heptadeca-1(13),2(6),7(12),10,16-pentaen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H20O4/c1-10-19(4,5)14-16(21-10)12-8-9-18(2,3)23-15(12)11-6-7-13(20)22-17(11)14/h6-10H,1-5H3
InChI Key AOIFNIMKVOPLGP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O4
Molecular Weight 312.40 g/mol
Exact Mass 312.13615911 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.04
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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139726-52-6
AKOS040735890
4,5,5,15,15-pentamethyl-3,8,14-trioxatetracyclo[11.4.0.02,6.07,12]heptadeca-1(13),2(6),7(12),10,16-pentaen-9-one

2D Structure

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2D Structure of Citrusarin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.6367 63.67%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7124 71.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9042 90.42%
OATP1B3 inhibitior + 0.9741 97.41%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6191 61.91%
P-glycoprotein inhibitior - 0.5092 50.92%
P-glycoprotein substrate - 0.6071 60.71%
CYP3A4 substrate + 0.5544 55.44%
CYP2C9 substrate - 0.6696 66.96%
CYP2D6 substrate - 0.8440 84.40%
CYP3A4 inhibition + 0.6080 60.80%
CYP2C9 inhibition + 0.5666 56.66%
CYP2C19 inhibition + 0.6628 66.28%
CYP2D6 inhibition - 0.8474 84.74%
CYP1A2 inhibition + 0.7174 71.74%
CYP2C8 inhibition - 0.8009 80.09%
CYP inhibitory promiscuity + 0.6918 69.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.5314 53.14%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.6262 62.62%
Skin irritation - 0.6720 67.20%
Skin corrosion - 0.9478 94.78%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4532 45.32%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.7198 71.98%
skin sensitisation - 0.6778 67.78%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.4712 47.12%
Acute Oral Toxicity (c) III 0.4113 41.13%
Estrogen receptor binding + 0.9318 93.18%
Androgen receptor binding + 0.6326 63.26%
Thyroid receptor binding + 0.5936 59.36%
Glucocorticoid receptor binding + 0.7440 74.40%
Aromatase binding + 0.8572 85.72%
PPAR gamma + 0.8808 88.08%
Honey bee toxicity - 0.8342 83.42%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9936 99.36%

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 93.41% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.49% 99.23%
CHEMBL2581 P07339 Cathepsin D 92.04% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.86% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.15% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.66% 94.45%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.85% 95.71%

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.
Citrus medica

Cross-Links

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PubChem 15108309
LOTUS LTS0186542
wikiData Q104915687