Cis-Dihydrohomoanatoxin-A

Details

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Internal ID b4eba263-3d45-4868-b241-73378dcccb5b
Taxonomy Organoheterocyclic compounds > Azepanes
IUPAC Name 1-[(1R,2S,6R)-9-azabicyclo[4.2.1]nonan-2-yl]propan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H19NO/c1-2-11(13)9-5-3-4-8-6-7-10(9)12-8/h8-10,12H,2-7H2,1H3/t8-,9+,10-/m1/s1
InChI Key MVXJVRNMGNXROR-KXUCPTDWSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H19NO
Molecular Weight 181.27 g/mol
Exact Mass 181.146664230 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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DTXSID801046665

2D Structure

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2D Structure of Cis-Dihydrohomoanatoxin-A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6965 69.65%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.6444 64.44%
OATP2B1 inhibitior - 0.8347 83.47%
OATP1B1 inhibitior + 0.9400 94.00%
OATP1B3 inhibitior + 0.9487 94.87%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.8493 84.93%
P-glycoprotein inhibitior - 0.9686 96.86%
P-glycoprotein substrate - 0.8179 81.79%
CYP3A4 substrate - 0.5794 57.94%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate + 0.3802 38.02%
CYP3A4 inhibition - 0.9643 96.43%
CYP2C9 inhibition - 0.8778 87.78%
CYP2C19 inhibition - 0.8189 81.89%
CYP2D6 inhibition - 0.8688 86.88%
CYP1A2 inhibition - 0.6320 63.20%
CYP2C8 inhibition - 0.8830 88.30%
CYP inhibitory promiscuity - 0.7375 73.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6805 68.05%
Eye corrosion - 0.8871 88.71%
Eye irritation + 0.7253 72.53%
Skin irritation - 0.6679 66.79%
Skin corrosion - 0.7552 75.52%
Ames mutagenesis - 0.5270 52.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5274 52.74%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.6053 60.53%
skin sensitisation - 0.8256 82.56%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.7493 74.93%
Acute Oral Toxicity (c) III 0.7130 71.30%
Estrogen receptor binding - 0.8566 85.66%
Androgen receptor binding - 0.6521 65.21%
Thyroid receptor binding - 0.8387 83.87%
Glucocorticoid receptor binding - 0.8470 84.70%
Aromatase binding - 0.6684 66.84%
PPAR gamma - 0.8129 81.29%
Honey bee toxicity - 0.9733 97.33%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.8556 85.56%

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 97.14% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.61% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.92% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.04% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 83.62% 95.93%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 83.55% 96.38%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.60% 93.03%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.51% 94.45%

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.
There are no matching plants.

Cross-Links

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PubChem 101942170
LOTUS LTS0160909
wikiData Q105173418