Norneolambertellin

Details

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Internal ID 6fbf0c07-4e5d-4716-a6ab-792a97b794c2
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Coumarino-alpha-pyrones
IUPAC Name 7-hydroxy-3-methylpyrano[3,2-c]chromene-2,5-dione
SMILES (Canonical) CC1=CC2=C(C3=C(C(=CC=C3)O)OC2=O)OC1=O
SMILES (Isomeric) CC1=CC2=C(C3=C(C(=CC=C3)O)OC2=O)OC1=O
InChI InChI=1S/C13H8O5/c1-6-5-8-10(17-12(6)15)7-3-2-4-9(14)11(7)18-13(8)16/h2-5,14H,1H3
InChI Key NZPWDOVJYOANMS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8O5
Molecular Weight 244.20 g/mol
Exact Mass 244.03717335 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.91
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEMBL452941

2D Structure

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2D Structure of Norneolambertellin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9546 95.46%
Caco-2 - 0.5769 57.69%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.7559 75.59%
OATP2B1 inhibitior - 0.7267 72.67%
OATP1B1 inhibitior + 0.9570 95.70%
OATP1B3 inhibitior + 0.9768 97.68%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8876 88.76%
P-glycoprotein inhibitior - 0.8832 88.32%
P-glycoprotein substrate - 0.9323 93.23%
CYP3A4 substrate - 0.5300 53.00%
CYP2C9 substrate - 0.6220 62.20%
CYP2D6 substrate - 0.8619 86.19%
CYP3A4 inhibition - 0.9049 90.49%
CYP2C9 inhibition - 0.7773 77.73%
CYP2C19 inhibition - 0.9514 95.14%
CYP2D6 inhibition - 0.9727 97.27%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.7856 78.56%
CYP inhibitory promiscuity - 0.9331 93.31%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5959 59.59%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.7765 77.65%
Skin irritation + 0.5680 56.80%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8166 81.66%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.5802 58.02%
skin sensitisation - 0.8748 87.48%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7692 76.92%
Acute Oral Toxicity (c) II 0.4827 48.27%
Estrogen receptor binding + 0.5907 59.07%
Androgen receptor binding + 0.6054 60.54%
Thyroid receptor binding - 0.5634 56.34%
Glucocorticoid receptor binding + 0.8371 83.71%
Aromatase binding + 0.5884 58.84%
PPAR gamma + 0.7714 77.14%
Honey bee toxicity - 0.9576 95.76%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9443 94.43%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.77% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.96% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 94.93% 94.73%
CHEMBL2581 P07339 Cathepsin D 93.87% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.86% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.04% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.95% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.95% 99.15%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.36% 93.65%
CHEMBL1951 P21397 Monoamine oxidase A 86.09% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.88% 86.33%
CHEMBL2535 P11166 Glucose transporter 84.30% 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.
There are no matching plants.

Cross-Links

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PubChem 44587673
LOTUS LTS0050894
wikiData Q77502794