(8R)-1,9,13-trimethyl-8-(9-oxotridecyl)-1,5,9,13-tetrazacycloheptadecan-6-one

Details

Top
Internal ID 03022328-e1cb-4714-9693-8e17ed9a7531
Taxonomy Organic acids and derivatives > Carboximidic acids and derivatives > Carboximidic acids > Cyclic carboximidic acids
IUPAC Name (8R)-1,9,13-trimethyl-8-(9-oxotridecyl)-1,5,9,13-tetrazacycloheptadecan-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H58N4O2/c1-5-6-18-28(34)19-12-10-8-7-9-11-17-27-26-29(35)30-20-15-23-31(2)21-13-14-22-32(3)24-16-25-33(27)4/h27H,5-26H2,1-4H3,(H,30,35)/t27-/m1/s1
InChI Key JZYOIEIVFSLACH-HHHXNRCGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C29H58N4O2
Molecular Weight 494.80 g/mol
Exact Mass 494.45597711 g/mol
Topological Polar Surface Area (TPSA) 55.90 Ų
XlogP 5.10
Atomic LogP (AlogP) 5.11
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (8R)-1,9,13-trimethyl-8-(9-oxotridecyl)-1,5,9,13-tetrazacycloheptadecan-6-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9621 96.21%
Caco-2 - 0.6815 68.15%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.4841 48.41%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9111 91.11%
OATP1B3 inhibitior + 0.9204 92.04%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.8629 86.29%
P-glycoprotein inhibitior - 0.4903 49.03%
P-glycoprotein substrate + 0.6504 65.04%
CYP3A4 substrate + 0.5784 57.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6564 65.64%
CYP3A4 inhibition - 0.9583 95.83%
CYP2C9 inhibition - 0.9550 95.50%
CYP2C19 inhibition - 0.9403 94.03%
CYP2D6 inhibition - 0.8457 84.57%
CYP1A2 inhibition - 0.9212 92.12%
CYP2C8 inhibition - 0.9235 92.35%
CYP inhibitory promiscuity - 0.9958 99.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.6108 61.08%
Eye corrosion - 0.9762 97.62%
Eye irritation - 0.7349 73.49%
Skin irritation - 0.7694 76.94%
Skin corrosion - 0.7334 73.34%
Ames mutagenesis - 0.8032 80.32%
Human Ether-a-go-go-Related Gene inhibition - 0.7463 74.63%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.6449 64.49%
skin sensitisation - 0.9102 91.02%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.8029 80.29%
Acute Oral Toxicity (c) III 0.7067 70.67%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.7182 71.82%
Thyroid receptor binding + 0.5588 55.88%
Glucocorticoid receptor binding - 0.6185 61.85%
Aromatase binding - 0.4856 48.56%
PPAR gamma - 0.5397 53.97%
Honey bee toxicity - 0.9502 95.02%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6224 62.24%
Fish aquatic toxicity - 0.8705 87.05%

Targets

Top

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.46% 96.09%
CHEMBL2581 P07339 Cathepsin D 99.41% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.33% 97.25%
CHEMBL220 P22303 Acetylcholinesterase 97.80% 94.45%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 92.96% 91.81%
CHEMBL217 P14416 Dopamine D2 receptor 91.65% 95.62%
CHEMBL255 P29275 Adenosine A2b receptor 91.45% 98.59%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.86% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 88.85% 93.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.02% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.39% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.08% 99.23%
CHEMBL325 Q13547 Histone deacetylase 1 86.64% 95.92%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 86.45% 91.03%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.25% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.89% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.33% 90.71%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.04% 95.50%
CHEMBL4208 P20618 Proteasome component C5 84.41% 90.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.23% 90.08%
CHEMBL299 P17252 Protein kinase C alpha 82.74% 98.03%
CHEMBL5255 O00206 Toll-like receptor 4 82.31% 92.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.23% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.15% 100.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.51% 82.38%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.10% 93.99%

Plants that contains it

Top
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

Top
PubChem 163191066
LOTUS LTS0230428
wikiData Q105137721