1,9,13-Trimethyl-8-nonyl-1,5,9,13-tetrazacycloheptadecan-6-one

Details

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Internal ID f55fb691-2070-480a-b142-672457eb7b9c
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name 1,9,13-trimethyl-8-nonyl-1,5,9,13-tetrazacycloheptadecan-6-one
SMILES (Canonical) CCCCCCCCCC1CC(=O)NCCCN(CCCCN(CCCN1C)C)C
SMILES (Isomeric) CCCCCCCCCC1CC(=O)NCCCN(CCCCN(CCCN1C)C)C
InChI InChI=1S/C25H52N4O/c1-5-6-7-8-9-10-11-16-24-23-25(30)26-17-14-20-27(2)18-12-13-19-28(3)21-15-22-29(24)4/h24H,5-23H2,1-4H3,(H,26,30)
InChI Key OAURMGVSLFVKFS-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H52N4O
Molecular Weight 424.70 g/mol
Exact Mass 424.41411229 g/mol
Topological Polar Surface Area (TPSA) 38.80 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.37
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,9,13-Trimethyl-8-nonyl-1,5,9,13-tetrazacycloheptadecan-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9695 96.95%
Caco-2 - 0.5464 54.64%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.6794 67.94%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9316 93.16%
OATP1B3 inhibitior + 0.9286 92.86%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.7294 72.94%
P-glycoprotein inhibitior - 0.6927 69.27%
P-glycoprotein substrate + 0.6112 61.12%
CYP3A4 substrate + 0.5475 54.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3591 35.91%
CYP3A4 inhibition - 0.9874 98.74%
CYP2C9 inhibition - 0.9491 94.91%
CYP2C19 inhibition - 0.9593 95.93%
CYP2D6 inhibition - 0.7594 75.94%
CYP1A2 inhibition - 0.9041 90.41%
CYP2C8 inhibition - 0.9639 96.39%
CYP inhibitory promiscuity - 0.9963 99.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.6540 65.40%
Eye corrosion - 0.9480 94.80%
Eye irritation - 0.7201 72.01%
Skin irritation - 0.7227 72.27%
Skin corrosion - 0.6268 62.68%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6124 61.24%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.5949 59.49%
skin sensitisation - 0.9018 90.18%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6715 67.15%
Acute Oral Toxicity (c) III 0.7495 74.95%
Estrogen receptor binding + 0.6150 61.50%
Androgen receptor binding - 0.7051 70.51%
Thyroid receptor binding + 0.5300 53.00%
Glucocorticoid receptor binding - 0.7189 71.89%
Aromatase binding + 0.6134 61.34%
PPAR gamma - 0.5628 56.28%
Honey bee toxicity - 0.9516 95.16%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6037 60.37%
Fish aquatic toxicity - 0.8234 82.34%

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
CHEMBL2581 P07339 Cathepsin D 99.39% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.93% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.81% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 95.63% 91.81%
CHEMBL220 P22303 Acetylcholinesterase 92.62% 94.45%
CHEMBL255 P29275 Adenosine A2b receptor 92.11% 98.59%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.13% 92.86%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 90.59% 100.00%
CHEMBL228 P31645 Serotonin transporter 89.18% 95.51%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 88.67% 91.03%
CHEMBL217 P14416 Dopamine D2 receptor 87.70% 95.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.45% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.43% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 87.04% 90.08%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.02% 93.99%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.55% 95.89%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.43% 93.00%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 85.19% 90.24%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.81% 95.50%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.80% 90.71%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.14% 82.38%
CHEMBL1978 P11511 Cytochrome P450 19A1 81.37% 91.76%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 81.28% 97.64%

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.
Albizia amara

Cross-Links

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PubChem 10455058
LOTUS LTS0168495
wikiData Q105188825