4,25,25-Trimethyl-26,27-dioxa-8-azaheptacyclo[22.2.1.01,21.04,20.05,17.07,15.09,14]heptacosa-5,7(15),9,11,13,16,21-heptaen-23-one

Details

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Internal ID 53c71f6e-85df-4442-95b0-b397584ddfee
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name 4,25,25-trimethyl-26,27-dioxa-8-azaheptacyclo[22.2.1.01,21.04,20.05,17.07,15.09,14]heptacosa-5,7(15),9,11,13,16,21-heptaen-23-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H27NO3/c1-25(2)24-23(29)14-20-18-9-8-15-12-17-16-6-4-5-7-21(16)28-22(17)13-19(15)26(18,3)10-11-27(20,30-24)31-25/h4-7,12-14,18,24,28H,8-11H2,1-3H3
InChI Key LXVZDJWVNOXLAL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H27NO3
Molecular Weight 413.50 g/mol
Exact Mass 413.19909372 g/mol
Topological Polar Surface Area (TPSA) 51.30 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.33
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,25,25-Trimethyl-26,27-dioxa-8-azaheptacyclo[22.2.1.01,21.04,20.05,17.07,15.09,14]heptacosa-5,7(15),9,11,13,16,21-heptaen-23-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 - 0.6083 60.83%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6310 63.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7926 79.26%
OATP1B3 inhibitior + 0.9502 95.02%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.9870 98.70%
P-glycoprotein inhibitior + 0.8656 86.56%
P-glycoprotein substrate + 0.5152 51.52%
CYP3A4 substrate + 0.7126 71.26%
CYP2C9 substrate - 0.8081 80.81%
CYP2D6 substrate - 0.8596 85.96%
CYP3A4 inhibition - 0.8534 85.34%
CYP2C9 inhibition - 0.7794 77.94%
CYP2C19 inhibition - 0.6557 65.57%
CYP2D6 inhibition - 0.8084 80.84%
CYP1A2 inhibition + 0.6636 66.36%
CYP2C8 inhibition + 0.6789 67.89%
CYP inhibitory promiscuity - 0.5573 55.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5621 56.21%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9722 97.22%
Skin irritation - 0.7454 74.54%
Skin corrosion - 0.9281 92.81%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8709 87.09%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5290 52.90%
skin sensitisation - 0.7665 76.65%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.7070 70.70%
Acute Oral Toxicity (c) III 0.5429 54.29%
Estrogen receptor binding + 0.8613 86.13%
Androgen receptor binding + 0.7433 74.33%
Thyroid receptor binding + 0.8176 81.76%
Glucocorticoid receptor binding + 0.8597 85.97%
Aromatase binding + 0.6673 66.73%
PPAR gamma + 0.7199 71.99%
Honey bee toxicity - 0.7553 75.53%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9865 98.65%

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 99.57% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.35% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.10% 95.56%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 95.25% 94.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.96% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 93.93% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.05% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.95% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.57% 99.23%
CHEMBL2581 P07339 Cathepsin D 88.94% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.07% 89.00%
CHEMBL4040 P28482 MAP kinase ERK2 86.69% 83.82%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.95% 94.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.32% 95.89%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 84.68% 94.08%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.62% 93.40%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 84.44% 96.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.83% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.13% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.98% 92.62%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.53% 92.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.31% 94.00%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 81.20% 90.71%
CHEMBL2803 P43403 Tyrosine-protein kinase ZAP-70 80.99% 82.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.23% 85.14%

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 162814230
LOTUS LTS0262366
wikiData Q105159102