3,13,17,27-Tetramethyl-1,15-diazacyclooctacosa-3,5,7,9,11,17,19,21,23,25-decaene-2,16-dione

Details

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Internal ID 7e005c04-2e63-47bb-9fcf-9e1825a48500
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name 3,13,17,27-tetramethyl-1,15-diazacyclooctacosa-3,5,7,9,11,17,19,21,23,25-decaene-2,16-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H38N2O2/c1-25-19-15-11-7-5-9-13-18-22-28(4)30(34)32-24-26(2)20-16-12-8-6-10-14-17-21-27(3)29(33)31-23-25/h5-22,25-26H,23-24H2,1-4H3,(H,31,33)(H,32,34)
InChI Key AOPCXXMLGSMDPM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H38N2O2
Molecular Weight 458.60 g/mol
Exact Mass 458.293328459 g/mol
Topological Polar Surface Area (TPSA) 58.20 Ų
XlogP 7.90
Atomic LogP (AlogP) 5.85
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,13,17,27-Tetramethyl-1,15-diazacyclooctacosa-3,5,7,9,11,17,19,21,23,25-decaene-2,16-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9827 98.27%
Caco-2 + 0.5114 51.14%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.4992 49.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9340 93.40%
OATP1B3 inhibitior + 0.9417 94.17%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9729 97.29%
P-glycoprotein inhibitior + 0.8311 83.11%
P-glycoprotein substrate - 0.8611 86.11%
CYP3A4 substrate - 0.5952 59.52%
CYP2C9 substrate - 0.6203 62.03%
CYP2D6 substrate - 0.9089 90.89%
CYP3A4 inhibition - 0.9604 96.04%
CYP2C9 inhibition - 0.7923 79.23%
CYP2C19 inhibition - 0.8135 81.35%
CYP2D6 inhibition - 0.9060 90.60%
CYP1A2 inhibition - 0.7877 78.77%
CYP2C8 inhibition - 0.9690 96.90%
CYP inhibitory promiscuity - 0.9688 96.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7253 72.53%
Carcinogenicity (trinary) Non-required 0.4157 41.57%
Eye corrosion - 0.9099 90.99%
Eye irritation - 0.9539 95.39%
Skin irritation - 0.7315 73.15%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9480 94.80%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8257 82.57%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6393 63.93%
Acute Oral Toxicity (c) III 0.5964 59.64%
Estrogen receptor binding + 0.5921 59.21%
Androgen receptor binding - 0.5990 59.90%
Thyroid receptor binding + 0.6155 61.55%
Glucocorticoid receptor binding - 0.6296 62.96%
Aromatase binding - 0.4917 49.17%
PPAR gamma + 0.6030 60.30%
Honey bee toxicity - 0.8896 88.96%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity - 0.7471 74.71%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.76% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.80% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.14% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 86.97% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.59% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.57% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.10% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.68% 94.80%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.73% 90.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.00% 91.11%

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 163077152
LOTUS LTS0039409
wikiData Q103816295