Norpenicyrone

Details

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Internal ID 7d0daa76-faa0-4806-b3d3-73861cabc714
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 6-[(2S,3E,6E)-2,5-dihydroxy-4,6-dimethyl-7-[(1S,2S,4R,5R)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]hepta-3,6-dien-2-yl]-4-methoxy-5-methylpyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H32O7/c1-12(10-21(5,26)19-14(3)16(27-8)9-17(24)28-19)18(25)13(2)11-22(6)20-23(7,30-20)15(4)29-22/h9-11,15,18,20,25-26H,1-8H3/b12-10+,13-11+/t15-,18?,20+,21+,22+,23-/m1/s1
InChI Key LCCPPRXJAQXPDH-JATQDRHESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H32O7
Molecular Weight 420.50 g/mol
Exact Mass 420.21480336 g/mol
Topological Polar Surface Area (TPSA) 97.80 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.75
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Norpenicyrone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9672 96.72%
Caco-2 - 0.5958 59.58%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7171 71.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8959 89.59%
OATP1B3 inhibitior + 0.9096 90.96%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7480 74.80%
P-glycoprotein inhibitior + 0.6011 60.11%
P-glycoprotein substrate - 0.5520 55.20%
CYP3A4 substrate + 0.6482 64.82%
CYP2C9 substrate - 0.6358 63.58%
CYP2D6 substrate - 0.8443 84.43%
CYP3A4 inhibition - 0.5193 51.93%
CYP2C9 inhibition - 0.7655 76.55%
CYP2C19 inhibition + 0.7208 72.08%
CYP2D6 inhibition - 0.8403 84.03%
CYP1A2 inhibition - 0.7586 75.86%
CYP2C8 inhibition + 0.4914 49.14%
CYP inhibitory promiscuity + 0.6933 69.33%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Danger 0.6256 62.56%
Eye corrosion - 0.9831 98.31%
Eye irritation - 0.8861 88.61%
Skin irritation - 0.7028 70.28%
Skin corrosion - 0.9494 94.94%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4842 48.42%
Micronuclear + 0.7000 70.00%
Hepatotoxicity - 0.5333 53.33%
skin sensitisation - 0.7358 73.58%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.6412 64.12%
Acute Oral Toxicity (c) III 0.3838 38.38%
Estrogen receptor binding + 0.8037 80.37%
Androgen receptor binding + 0.6751 67.51%
Thyroid receptor binding + 0.6410 64.10%
Glucocorticoid receptor binding + 0.7523 75.23%
Aromatase binding + 0.7110 71.10%
PPAR gamma + 0.8266 82.66%
Honey bee toxicity - 0.6108 61.08%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9566 95.66%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.40% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.75% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.74% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.13% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.36% 94.45%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 90.71% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.54% 89.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 87.05% 89.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.87% 86.33%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 86.85% 92.88%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.29% 91.07%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.97% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.81% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.70% 94.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.07% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.76% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 84.23% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.12% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 83.56% 94.73%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.64% 97.28%
CHEMBL4040 P28482 MAP kinase ERK2 82.45% 83.82%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.28% 96.21%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.24% 92.94%
CHEMBL2535 P11166 Glucose transporter 81.17% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.61% 97.09%

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 146684049
LOTUS LTS0198742
wikiData Q105149769