(2Z)-Farnesylamine

Details

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Internal ID 9930f8ef-295e-4a61-97d0-6344b1ceca7c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2Z)-3,7,11-trimethyldodeca-2,6,10-trien-1-amine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H27N/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11H,5-6,8,10,12,16H2,1-4H3/b14-9?,15-11-
InChI Key BDKQVCHNTAJNJR-ONUHYBHYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H27N
Molecular Weight 221.38 g/mol
Exact Mass 221.214349865 g/mol
Topological Polar Surface Area (TPSA) 26.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.36
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2Z)-Farnesylamine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9743 97.43%
Caco-2 + 0.9379 93.79%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.7666 76.66%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.9592 95.92%
OATP1B3 inhibitior + 0.9472 94.72%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.7315 73.15%
P-glycoprotein inhibitior - 0.9463 94.63%
P-glycoprotein substrate - 0.9571 95.71%
CYP3A4 substrate - 0.6794 67.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4589 45.89%
CYP3A4 inhibition - 0.9210 92.10%
CYP2C9 inhibition - 0.8498 84.98%
CYP2C19 inhibition - 0.8600 86.00%
CYP2D6 inhibition - 0.7946 79.46%
CYP1A2 inhibition - 0.5964 59.64%
CYP2C8 inhibition - 0.9689 96.89%
CYP inhibitory promiscuity - 0.7423 74.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.5344 53.44%
Eye corrosion + 0.7546 75.46%
Eye irritation + 0.6361 63.61%
Skin irritation + 0.8014 80.14%
Skin corrosion + 0.8248 82.48%
Ames mutagenesis - 0.8483 84.83%
Human Ether-a-go-go-Related Gene inhibition - 0.4006 40.06%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation + 0.7667 76.67%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.5268 52.68%
Acute Oral Toxicity (c) III 0.6694 66.94%
Estrogen receptor binding - 0.8962 89.62%
Androgen receptor binding - 0.8143 81.43%
Thyroid receptor binding - 0.7639 76.39%
Glucocorticoid receptor binding + 0.5390 53.90%
Aromatase binding - 0.6947 69.47%
PPAR gamma + 0.7096 70.96%
Honey bee toxicity - 0.8949 89.49%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9477 94.77%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.38% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.15% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.23% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 83.41% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.28% 96.95%
CHEMBL221 P23219 Cyclooxygenase-1 81.70% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.87% 99.17%

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 129653587
LOTUS LTS0226018
wikiData Q105100565