(3R,6S,12Z)-12-benzylidene-1,6,7-trimethyl-3-(2-methylpropyl)-1,4,7,10-tetrazacyclododecane-2,5,8,11-tetrone

Details

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Internal ID 961166d5-d2d7-453c-9a27-3089d645e470
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name (3R,6S,12Z)-12-benzylidene-1,6,7-trimethyl-3-(2-methylpropyl)-1,4,7,10-tetrazacyclododecane-2,5,8,11-tetrone
SMILES (Canonical) CC1C(=O)NC(C(=O)N(C(=CC2=CC=CC=C2)C(=O)NCC(=O)N1C)C)CC(C)C
SMILES (Isomeric) C[C@H]1C(=O)N[C@@H](C(=O)N(/C(=C\C2=CC=CC=C2)/C(=O)NCC(=O)N1C)C)CC(C)C
InChI InChI=1S/C22H30N4O4/c1-14(2)11-17-22(30)26(5)18(12-16-9-7-6-8-10-16)21(29)23-13-19(27)25(4)15(3)20(28)24-17/h6-10,12,14-15,17H,11,13H2,1-5H3,(H,23,29)(H,24,28)/b18-12-/t15-,17+/m0/s1
InChI Key SIIRBDOFKDACOK-OVGQPCSFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H30N4O4
Molecular Weight 414.50 g/mol
Exact Mass 414.22670545 g/mol
Topological Polar Surface Area (TPSA) 98.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 0.99
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,6S,12Z)-12-benzylidene-1,6,7-trimethyl-3-(2-methylpropyl)-1,4,7,10-tetrazacyclododecane-2,5,8,11-tetrone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9698 96.98%
Caco-2 + 0.7122 71.22%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4939 49.39%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.8894 88.94%
OATP1B3 inhibitior + 0.9205 92.05%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8350 83.50%
P-glycoprotein inhibitior + 0.6375 63.75%
P-glycoprotein substrate + 0.9344 93.44%
CYP3A4 substrate + 0.5635 56.35%
CYP2C9 substrate + 0.5905 59.05%
CYP2D6 substrate - 0.8727 87.27%
CYP3A4 inhibition - 0.6726 67.26%
CYP2C9 inhibition - 0.8538 85.38%
CYP2C19 inhibition - 0.7171 71.71%
CYP2D6 inhibition - 0.9304 93.04%
CYP1A2 inhibition - 0.7870 78.70%
CYP2C8 inhibition - 0.7605 76.05%
CYP inhibitory promiscuity - 0.9317 93.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8323 83.23%
Carcinogenicity (trinary) Non-required 0.6069 60.69%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.9944 99.44%
Skin irritation - 0.7435 74.35%
Skin corrosion - 0.9120 91.20%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6806 68.06%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.5541 55.41%
skin sensitisation - 0.8562 85.62%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.7221 72.21%
Acute Oral Toxicity (c) III 0.6645 66.45%
Estrogen receptor binding - 0.6312 63.12%
Androgen receptor binding + 0.7971 79.71%
Thyroid receptor binding - 0.5450 54.50%
Glucocorticoid receptor binding + 0.5762 57.62%
Aromatase binding - 0.5994 59.94%
PPAR gamma + 0.6629 66.29%
Honey bee toxicity - 0.8641 86.41%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity - 0.3690 36.90%

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 99.36% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.67% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.97% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.56% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.66% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.02% 91.11%
CHEMBL321 P14780 Matrix metalloproteinase 9 89.37% 92.12%
CHEMBL333 P08253 Matrix metalloproteinase-2 88.45% 96.31%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.85% 93.00%
CHEMBL1937 Q92769 Histone deacetylase 2 87.39% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.63% 93.99%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 85.97% 89.67%
CHEMBL221 P23219 Cyclooxygenase-1 85.08% 90.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.86% 89.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.96% 90.08%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.93% 96.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.23% 96.47%
CHEMBL3524 P56524 Histone deacetylase 4 81.07% 92.97%

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.
Micromeles japonica

Cross-Links

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PubChem 163186995
LOTUS LTS0013998
wikiData Q105253774