8-(6-Hydroxypentadecyl)-1,13-dimethyl-1,5,9,13-tetrazacycloheptadecan-6-one

Details

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Internal ID a87e132f-c2a6-47f5-8ad3-87ea99544cb9
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name 8-(6-hydroxypentadecyl)-1,13-dimethyl-1,5,9,13-tetrazacycloheptadecan-6-one
SMILES (Canonical) CCCCCCCCCC(CCCCCC1CC(=O)NCCCN(CCCCN(CCCN1)C)C)O
SMILES (Isomeric) CCCCCCCCCC(CCCCCC1CC(=O)NCCCN(CCCCN(CCCN1)C)C)O
InChI InChI=1S/C30H62N4O2/c1-4-5-6-7-8-9-12-19-29(35)20-13-10-11-18-28-27-30(36)32-22-17-26-34(3)24-15-14-23-33(2)25-16-21-31-28/h28-29,31,35H,4-27H2,1-3H3,(H,32,36)
InChI Key PNURFNPZVHXXPD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H62N4O2
Molecular Weight 510.80 g/mol
Exact Mass 510.48727723 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.34
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-(6-Hydroxypentadecyl)-1,13-dimethyl-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 + 0.8904 89.04%
Caco-2 - 0.7792 77.92%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.5294 52.94%
OATP2B1 inhibitior + 0.5723 57.23%
OATP1B1 inhibitior + 0.9384 93.84%
OATP1B3 inhibitior + 0.9174 91.74%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6037 60.37%
P-glycoprotein inhibitior - 0.5397 53.97%
P-glycoprotein substrate + 0.7323 73.23%
CYP3A4 substrate + 0.5827 58.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3962 39.62%
CYP3A4 inhibition - 0.9657 96.57%
CYP2C9 inhibition - 0.9291 92.91%
CYP2C19 inhibition - 0.9368 93.68%
CYP2D6 inhibition - 0.7835 78.35%
CYP1A2 inhibition - 0.9077 90.77%
CYP2C8 inhibition - 0.9356 93.56%
CYP inhibitory promiscuity - 0.9943 99.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.6015 60.15%
Eye corrosion - 0.9724 97.24%
Eye irritation - 0.8444 84.44%
Skin irritation - 0.7530 75.30%
Skin corrosion - 0.7092 70.92%
Ames mutagenesis - 0.7854 78.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7436 74.36%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.5909 59.09%
skin sensitisation - 0.8861 88.61%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.7487 74.87%
Acute Oral Toxicity (c) III 0.6892 68.92%
Estrogen receptor binding + 0.5522 55.22%
Androgen receptor binding - 0.5648 56.48%
Thyroid receptor binding + 0.5925 59.25%
Glucocorticoid receptor binding - 0.4759 47.59%
Aromatase binding + 0.6297 62.97%
PPAR gamma + 0.6091 60.91%
Honey bee toxicity - 0.9555 95.55%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5148 51.48%
Fish aquatic toxicity - 0.9438 94.38%

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 99.74% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.21% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.13% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.32% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 93.05% 91.81%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.96% 90.71%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 90.93% 100.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.51% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.07% 85.14%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 87.59% 91.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.36% 97.09%
CHEMBL5103 Q969S8 Histone deacetylase 10 87.10% 90.08%
CHEMBL255 P29275 Adenosine A2b receptor 86.48% 98.59%
CHEMBL4227 P25090 Lipoxin A4 receptor 85.91% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.87% 94.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.87% 97.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.69% 93.56%
CHEMBL4040 P28482 MAP kinase ERK2 85.64% 83.82%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.61% 95.89%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 85.13% 90.24%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.89% 93.03%
CHEMBL217 P14416 Dopamine D2 receptor 83.73% 95.62%
CHEMBL230 P35354 Cyclooxygenase-2 83.42% 89.63%
CHEMBL299 P17252 Protein kinase C alpha 83.34% 98.03%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.03% 89.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.28% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.87% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.25% 99.23%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.42% 93.00%

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 gummifera
Albizia schimperiana

Cross-Links

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PubChem 44566832
LOTUS LTS0266275
wikiData Q105212215