1-(Chloromethyl)-5-methylideneazocane

Details

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Internal ID ff4869f7-034a-45eb-b108-d104c0ec785a
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Amines > Tertiary amines > Trialkylamines
IUPAC Name 1-(chloromethyl)-5-methylideneazocane
SMILES (Canonical) C=C1CCCN(CCC1)CCl
SMILES (Isomeric) C=C1CCCN(CCC1)CCl
InChI InChI=1S/C9H16ClN/c1-9-4-2-6-11(8-10)7-3-5-9/h1-8H2
InChI Key WWOKLCSYRUIMIE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16ClN
Molecular Weight 173.68 g/mol
Exact Mass 173.0971272 g/mol
Topological Polar Surface Area (TPSA) 3.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(Chloromethyl)-5-methylideneazocane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9546 95.46%
Caco-2 + 0.6639 66.39%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Lysosomes 0.4996 49.96%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.9688 96.88%
OATP1B3 inhibitior + 0.9477 94.77%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior + 0.6250 62.50%
BSEP inhibitior - 0.8609 86.09%
P-glycoprotein inhibitior - 0.9794 97.94%
P-glycoprotein substrate - 0.9590 95.90%
CYP3A4 substrate - 0.7075 70.75%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate + 0.4421 44.21%
CYP3A4 inhibition - 0.8747 87.47%
CYP2C9 inhibition - 0.8759 87.59%
CYP2C19 inhibition - 0.6596 65.96%
CYP2D6 inhibition - 0.7663 76.63%
CYP1A2 inhibition - 0.5483 54.83%
CYP2C8 inhibition - 0.9923 99.23%
CYP inhibitory promiscuity - 0.5789 57.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7213 72.13%
Carcinogenicity (trinary) Non-required 0.3698 36.98%
Eye corrosion - 0.7424 74.24%
Eye irritation + 0.9670 96.70%
Skin irritation + 0.5740 57.40%
Skin corrosion + 0.6155 61.55%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5208 52.08%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7810 78.10%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.5786 57.86%
Acute Oral Toxicity (c) III 0.4811 48.11%
Estrogen receptor binding - 0.9581 95.81%
Androgen receptor binding - 0.9361 93.61%
Thyroid receptor binding - 0.8118 81.18%
Glucocorticoid receptor binding - 0.6829 68.29%
Aromatase binding - 0.7533 75.33%
PPAR gamma - 0.8733 87.33%
Honey bee toxicity - 0.9497 94.97%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.6804 68.04%

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
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.54% 93.40%
CHEMBL2581 P07339 Cathepsin D 88.13% 98.95%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 87.89% 95.34%
CHEMBL1978 P11511 Cytochrome P450 19A1 87.77% 91.76%
CHEMBL2885 P07451 Carbonic anhydrase III 80.32% 87.45%

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.
Lotononis oxyptera

Cross-Links

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PubChem 101625140
LOTUS LTS0027084
wikiData Q104400228