Cyclohexylamine

Details

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Internal ID a239379d-efed-4b62-b0a8-4d9379b20400
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Cyclohexylamines
IUPAC Name cyclohexanamine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H13N/c7-6-4-2-1-3-5-6/h6H,1-5,7H2
InChI Key PAFZNILMFXTMIY-UHFFFAOYSA-N
Popularity 4,384 references in papers

Physical and Chemical Properties

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Molecular Formula C6H13N
Molecular Weight 99.17 g/mol
Exact Mass 99.104799419 g/mol
Topological Polar Surface Area (TPSA) 26.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.28
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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Cyclohexanamine
108-91-8
Aminocyclohexane
Hexahydroaniline
Hexahydrobenzenamine
Aminohexahydrobenzene
1-Cyclohexylamine
Cyclohexyl amine
1-Aminocyclohexane
Aniline, hexahydro-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclohexylamine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.7390 73.90%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.8975 89.75%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9840 98.40%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.9545 95.45%
P-glycoprotein inhibitior - 0.9876 98.76%
P-glycoprotein substrate - 0.9876 98.76%
CYP3A4 substrate - 0.7931 79.31%
CYP2C9 substrate - 0.8281 82.81%
CYP2D6 substrate + 0.4796 47.96%
CYP3A4 inhibition - 0.9864 98.64%
CYP2C9 inhibition - 0.9707 97.07%
CYP2C19 inhibition - 0.8814 88.14%
CYP2D6 inhibition - 0.9171 91.71%
CYP1A2 inhibition - 0.5770 57.70%
CYP2C8 inhibition - 0.9572 95.72%
CYP inhibitory promiscuity - 0.8866 88.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.7213 72.13%
Eye corrosion + 0.9958 99.58%
Eye irritation + 0.9679 96.79%
Skin irritation + 0.8606 86.06%
Skin corrosion + 0.9883 98.83%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6360 63.60%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6657 66.57%
skin sensitisation - 0.8964 89.64%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.5761 57.61%
Acute Oral Toxicity (c) I 0.7818 78.18%
Estrogen receptor binding - 0.9053 90.53%
Androgen receptor binding - 0.9041 90.41%
Thyroid receptor binding - 0.8319 83.19%
Glucocorticoid receptor binding - 0.8138 81.38%
Aromatase binding - 0.8486 84.86%
PPAR gamma - 0.9154 91.54%
Honey bee toxicity - 0.8391 83.91%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity - 0.4317 43.17%

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 96.20% 97.09%
CHEMBL3012 Q13946 Phosphodiesterase 7A 89.28% 99.29%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.09% 92.94%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.39% 99.18%
CHEMBL1968 P07099 Epoxide hydrolase 1 82.75% 98.57%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.74% 96.09%
CHEMBL2147 P11309 Serine/threonine-protein kinase PIM1 81.90% 97.95%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.88% 95.50%
CHEMBL3384 Q16512 Protein kinase N1 80.90% 80.71%

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.
Zanthoxylum asiaticum

Cross-Links

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PubChem 7965
LOTUS LTS0253345
wikiData Q1147539