Flupyranochromene

Details

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Internal ID c2c92eb6-aa3f-4ad0-a7ab-8afea4f7e0a0
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 1,7,8-trihydroxy-3-methyl-10-oxo-1H-pyrano[4,3-b]chromene-9-carboxylic acid
SMILES (Canonical) CC1=CC2=C(C(O1)O)C(=O)C3=C(O2)C=C(C(=C3C(=O)O)O)O
SMILES (Isomeric) CC1=CC2=C(C(O1)O)C(=O)C3=C(O2)C=C(C(=C3C(=O)O)O)O
InChI InChI=1S/C14H10O8/c1-4-2-6-9(14(20)21-4)12(17)8-7(22-6)3-5(15)11(16)10(8)13(18)19/h2-3,14-16,20H,1H3,(H,18,19)
InChI Key FUFBBQLNHINKIH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H10O8
Molecular Weight 306.22 g/mol
Exact Mass 306.03756727 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.28
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Flupyranochromene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8608 86.08%
Caco-2 + 0.5338 53.38%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.5999 59.99%
OATP2B1 inhibitior - 0.6913 69.13%
OATP1B1 inhibitior + 0.8842 88.42%
OATP1B3 inhibitior + 0.9834 98.34%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8675 86.75%
P-glycoprotein inhibitior - 0.8623 86.23%
P-glycoprotein substrate - 0.7760 77.60%
CYP3A4 substrate - 0.5095 50.95%
CYP2C9 substrate + 0.5861 58.61%
CYP2D6 substrate - 0.8964 89.64%
CYP3A4 inhibition - 0.7784 77.84%
CYP2C9 inhibition - 0.6208 62.08%
CYP2C19 inhibition - 0.7638 76.38%
CYP2D6 inhibition - 0.9552 95.52%
CYP1A2 inhibition - 0.7619 76.19%
CYP2C8 inhibition - 0.6152 61.52%
CYP inhibitory promiscuity - 0.7118 71.18%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5102 51.02%
Eye corrosion - 0.9904 99.04%
Eye irritation + 0.5744 57.44%
Skin irritation - 0.5443 54.43%
Skin corrosion - 0.8898 88.98%
Ames mutagenesis + 0.5486 54.86%
Human Ether-a-go-go-Related Gene inhibition - 0.7871 78.71%
Micronuclear + 0.8900 89.00%
Hepatotoxicity - 0.5289 52.89%
skin sensitisation - 0.7159 71.59%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7689 76.89%
Acute Oral Toxicity (c) II 0.3737 37.37%
Estrogen receptor binding + 0.6529 65.29%
Androgen receptor binding + 0.6407 64.07%
Thyroid receptor binding - 0.6644 66.44%
Glucocorticoid receptor binding + 0.7940 79.40%
Aromatase binding + 0.6087 60.87%
PPAR gamma + 0.6623 66.23%
Honey bee toxicity - 0.9260 92.60%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9823 98.23%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.94% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.79% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.48% 89.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 92.63% 94.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.00% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.62% 99.23%
CHEMBL3194 P02766 Transthyretin 89.08% 90.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.36% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.58% 99.15%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.72% 81.11%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 82.66% 90.93%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.53% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.35% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 81.82% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.73% 86.33%
CHEMBL2581 P07339 Cathepsin D 80.21% 98.95%

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 145720686
LOTUS LTS0042777
wikiData Q105338850