1-(2-Acetoxyethyl)-3,6-diazahomoadamantan-9-one oxime

Details

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Internal ID 3bc9c812-767f-481e-9479-731361610284
Taxonomy Organoheterocyclic compounds > Diazepanes > 1,4-diazepanes
IUPAC Name 2-(9-hydroxyimino-3,6-diazatricyclo[4.3.1.13,8]undecan-1-yl)ethyl acetate
SMILES (Canonical) CC(=O)OCCC12CN3CCN(C1)CC(C3)C2=NO
SMILES (Isomeric) CC(=O)OCCC12CN3CCN(C1)CC(C3)C2=NO
InChI InChI=1S/C13H21N3O3/c1-10(17)19-5-2-13-8-15-3-4-16(9-13)7-11(6-15)12(13)14-18/h11,18H,2-9H2,1H3
InChI Key AJPFDLSTNHSVQG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H21N3O3
Molecular Weight 267.32 g/mol
Exact Mass 267.15829154 g/mol
Topological Polar Surface Area (TPSA) 65.40 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.02
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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AJPFDLSTNHSVQG-OWBHPGMISA-N

2D Structure

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2D Structure of 1-(2-Acetoxyethyl)-3,6-diazahomoadamantan-9-one oxime

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6715 67.15%
Caco-2 + 0.4930 49.30%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5453 54.53%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.9528 95.28%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.6766 67.66%
P-glycoprotein inhibitior - 0.9404 94.04%
P-glycoprotein substrate - 0.7606 76.06%
CYP3A4 substrate + 0.5809 58.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7381 73.81%
CYP3A4 inhibition - 0.7887 78.87%
CYP2C9 inhibition - 0.8089 80.89%
CYP2C19 inhibition - 0.7973 79.73%
CYP2D6 inhibition - 0.7532 75.32%
CYP1A2 inhibition - 0.7912 79.12%
CYP2C8 inhibition - 0.9308 93.08%
CYP inhibitory promiscuity - 0.9053 90.53%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5734 57.34%
Eye corrosion - 0.9747 97.47%
Eye irritation - 0.8846 88.46%
Skin irritation - 0.7407 74.07%
Skin corrosion - 0.9168 91.68%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5590 55.90%
Micronuclear + 0.6600 66.00%
Hepatotoxicity - 0.5396 53.96%
skin sensitisation - 0.8105 81.05%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.6297 62.97%
Acute Oral Toxicity (c) III 0.6099 60.99%
Estrogen receptor binding - 0.7727 77.27%
Androgen receptor binding - 0.6015 60.15%
Thyroid receptor binding - 0.6587 65.87%
Glucocorticoid receptor binding - 0.6131 61.31%
Aromatase binding - 0.6195 61.95%
PPAR gamma - 0.6328 63.28%
Honey bee toxicity - 0.8588 85.88%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6750 67.50%
Fish aquatic toxicity + 0.7785 77.85%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.80% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.38% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.63% 98.95%
CHEMBL255 P29275 Adenosine A2b receptor 86.87% 98.59%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.51% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.71% 91.11%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.96% 93.10%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.71% 85.14%

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.
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 551906
NPASS NPC158228