Norviburtinal

Details

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Internal ID d2212697-ac73-4823-8586-117dc9a5501b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Aryl-aldehydes
IUPAC Name cyclopenta[c]pyran-7-carbaldehyde
SMILES (Canonical) C1=COC=C2C1=CC=C2C=O
SMILES (Isomeric) C1=COC=C2C1=CC=C2C=O
InChI InChI=1S/C9H6O2/c10-5-8-2-1-7-3-4-11-6-9(7)8/h1-6H
InChI Key VRMFZTBAWYVGGB-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C9H6O2
Molecular Weight 146.14 g/mol
Exact Mass 146.036779430 g/mol
Topological Polar Surface Area (TPSA) 30.20 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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85051-41-8
cyclopenta[c]pyran-7-carbaldehyde
Cyclopenta[c]pyran-7-carboxaldehyde
SCHEMBL96526
CHEMBL1996335
DTXSID20327807
NSC688276
AKOS030591612
NSC-688276
NCI60_031868

2D Structure

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2D Structure of Norviburtinal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.9557 95.57%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.4235 42.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7995 79.95%
OATP1B3 inhibitior + 0.9780 97.80%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8973 89.73%
P-glycoprotein inhibitior - 0.9759 97.59%
P-glycoprotein substrate - 0.9757 97.57%
CYP3A4 substrate - 0.6338 63.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7572 75.72%
CYP3A4 inhibition - 0.8092 80.92%
CYP2C9 inhibition - 0.8205 82.05%
CYP2C19 inhibition - 0.5115 51.15%
CYP2D6 inhibition - 0.8680 86.80%
CYP1A2 inhibition + 0.8232 82.32%
CYP2C8 inhibition - 0.6845 68.45%
CYP inhibitory promiscuity - 0.8540 85.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7432 74.32%
Carcinogenicity (trinary) Non-required 0.6378 63.78%
Eye corrosion + 0.8374 83.74%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9145 91.45%
Skin corrosion - 0.7721 77.21%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7305 73.05%
Micronuclear + 0.5282 52.82%
Hepatotoxicity + 0.6203 62.03%
skin sensitisation + 0.8310 83.10%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5917 59.17%
Acute Oral Toxicity (c) III 0.8412 84.12%
Estrogen receptor binding - 0.9104 91.04%
Androgen receptor binding - 0.4831 48.31%
Thyroid receptor binding - 0.7521 75.21%
Glucocorticoid receptor binding - 0.8788 87.88%
Aromatase binding - 0.6680 66.80%
PPAR gamma - 0.7279 72.79%
Honey bee toxicity - 0.9016 90.16%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity - 0.5353 53.53%

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
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 92.75% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.86% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.38% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 85.38% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.92% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.27% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.64% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 80.72% 94.73%

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.
Kigelia africana subsp. africana
Rehmannia glutinosa
Stereospermum acuminatissimum

Cross-Links

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PubChem 390664
NPASS NPC115859
LOTUS LTS0241806
wikiData Q72496900