(3R,9R)-3,9-Diamino-1,7-diazacyclododecane-2,8-dione

Details

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Internal ID 1a0df592-dea3-4124-a4d1-4cab1d582435
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name (3R,9R)-3,9-diamino-1,7-diazacyclododecane-2,8-dione
SMILES (Canonical) C1CC(C(=O)NCCCC(C(=O)NC1)N)N
SMILES (Isomeric) C1C[C@H](C(=O)NCCC[C@H](C(=O)NC1)N)N
InChI InChI=1S/C10H20N4O2/c11-7-3-1-5-13-10(16)8(12)4-2-6-14-9(7)15/h7-8H,1-6,11-12H2,(H,13,16)(H,14,15)/t7-,8-/m1/s1
InChI Key NWDFWCXKIDTJBA-HTQZYQBOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20N4O2
Molecular Weight 228.29 g/mol
Exact Mass 228.15862589 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP -1.70
Atomic LogP (AlogP) -1.55
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,9R)-3,9-Diamino-1,7-diazacyclododecane-2,8-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9527 95.27%
Caco-2 - 0.7132 71.32%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Nucleus 0.4033 40.33%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.9824 98.24%
OATP1B3 inhibitior + 0.9494 94.94%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8306 83.06%
P-glycoprotein inhibitior - 0.8945 89.45%
P-glycoprotein substrate - 0.9041 90.41%
CYP3A4 substrate - 0.7181 71.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7285 72.85%
CYP3A4 inhibition - 0.9646 96.46%
CYP2C9 inhibition - 0.9338 93.38%
CYP2C19 inhibition - 0.9017 90.17%
CYP2D6 inhibition - 0.9479 94.79%
CYP1A2 inhibition - 0.8899 88.99%
CYP2C8 inhibition - 0.9887 98.87%
CYP inhibitory promiscuity - 0.9895 98.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.6412 64.12%
Eye corrosion - 0.9360 93.60%
Eye irritation - 0.9253 92.53%
Skin irritation - 0.7263 72.63%
Skin corrosion - 0.8883 88.83%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6492 64.92%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.9067 90.67%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.5629 56.29%
Acute Oral Toxicity (c) III 0.5914 59.14%
Estrogen receptor binding - 0.5444 54.44%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5791 57.91%
Glucocorticoid receptor binding - 0.7322 73.22%
Aromatase binding - 0.7117 71.17%
PPAR gamma - 0.6939 69.39%
Honey bee toxicity - 0.9058 90.58%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.9759 97.59%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 97.56% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.92% 91.11%
CHEMBL3384 Q16512 Protein kinase N1 89.80% 80.71%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.59% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.81% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.80% 92.94%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 83.02% 97.64%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.14% 93.04%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.94% 90.08%
CHEMBL4979 P13866 Sodium/glucose cotransporter 1 81.28% 98.24%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.14% 93.03%
CHEMBL2581 P07339 Cathepsin D 80.41% 98.95%

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.
Dacrycarpus imbricatus

Cross-Links

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PubChem 101477400
NPASS NPC240889
LOTUS LTS0041799
wikiData Q105186541