(3S,9S,14aR)-9-benzyl-6,6-dimethyl-3-(6-oxooctyl)decahydro-pyrrolo(1,2-a)(1,4,7,10)tetraazacyclododecine-1,4,7,10-tetraone

Details

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Internal ID 2eff95b1-c2f9-4c9d-b9f4-41a4388e6612
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name (3S,9S,12R)-3-benzyl-6,6-dimethyl-9-(6-oxooctyl)-1,4,7,10-tetrazabicyclo[10.3.0]pentadecane-2,5,8,11-tetrone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H40N4O5/c1-4-20(33)14-9-6-10-15-21-24(34)31-28(2,3)27(37)30-22(18-19-12-7-5-8-13-19)26(36)32-17-11-16-23(32)25(35)29-21/h5,7-8,12-13,21-23H,4,6,9-11,14-18H2,1-3H3,(H,29,35)(H,30,37)(H,31,34)/t21-,22-,23+/m0/s1
InChI Key HNGIDTWZBOOVGG-RJGXRXQPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H40N4O5
Molecular Weight 512.60 g/mol
Exact Mass 512.29987039 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.03
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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(3S,9S,14aR)-9-benzyl-6,6-dimethyl-3-(6-oxooctyl)decahydro-pyrrolo[1,2-a][1,4,7,10]tetraazacyclododecine-1,4,7,10-tetraone

2D Structure

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2D Structure of (3S,9S,14aR)-9-benzyl-6,6-dimethyl-3-(6-oxooctyl)decahydro-pyrrolo(1,2-a)(1,4,7,10)tetraazacyclododecine-1,4,7,10-tetraone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9570 95.70%
Caco-2 - 0.8292 82.92%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5960 59.60%
OATP2B1 inhibitior - 0.7181 71.81%
OATP1B1 inhibitior + 0.8540 85.40%
OATP1B3 inhibitior + 0.9313 93.13%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7181 71.81%
P-glycoprotein inhibitior + 0.8247 82.47%
P-glycoprotein substrate + 0.7697 76.97%
CYP3A4 substrate + 0.6569 65.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7938 79.38%
CYP3A4 inhibition - 0.6559 65.59%
CYP2C9 inhibition - 0.7616 76.16%
CYP2C19 inhibition - 0.7271 72.71%
CYP2D6 inhibition - 0.8476 84.76%
CYP1A2 inhibition - 0.9359 93.59%
CYP2C8 inhibition + 0.6516 65.16%
CYP inhibitory promiscuity - 0.8435 84.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6801 68.01%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.9665 96.65%
Skin irritation - 0.7939 79.39%
Skin corrosion - 0.8939 89.39%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7771 77.71%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.5392 53.92%
skin sensitisation - 0.8806 88.06%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.6324 63.24%
Acute Oral Toxicity (c) III 0.6606 66.06%
Estrogen receptor binding + 0.6481 64.81%
Androgen receptor binding + 0.5391 53.91%
Thyroid receptor binding - 0.5837 58.37%
Glucocorticoid receptor binding + 0.5849 58.49%
Aromatase binding - 0.5627 56.27%
PPAR gamma + 0.5637 56.37%
Honey bee toxicity - 0.8680 86.80%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.8532 85.32%

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 99.51% 98.95%
CHEMBL3524 P56524 Histone deacetylase 4 99.20% 92.97%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.19% 96.09%
CHEMBL325 Q13547 Histone deacetylase 1 96.88% 95.92%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.25% 91.11%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 94.98% 97.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.99% 95.56%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 93.83% 82.38%
CHEMBL221 P23219 Cyclooxygenase-1 93.54% 90.17%
CHEMBL1902 P62942 FK506-binding protein 1A 93.34% 97.05%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.77% 82.69%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 91.53% 93.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.45% 95.89%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 89.21% 93.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.07% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.55% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.41% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.38% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.20% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.41% 99.23%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.10% 90.08%
CHEMBL4040 P28482 MAP kinase ERK2 82.85% 83.82%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 82.73% 97.50%
CHEMBL3202 P48147 Prolyl endopeptidase 82.73% 90.65%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.56% 92.67%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.22% 100.00%

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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Cross-Links

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PubChem 71663569
LOTUS LTS0089968
wikiData Q75069484