Farnesyl isothiocyanate

Details

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Internal ID 7626aa0d-877f-4512-9336-dcbc998e8f6c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-isothiocyanato-3,7,11-trimethyldodeca-2,6,10-triene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H25NS/c1-14(2)7-5-8-15(3)9-6-10-16(4)11-12-17-13-18/h7,9,11H,5-6,8,10,12H2,1-4H3
InChI Key CVMJPEWSWVIBKI-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H25NS
Molecular Weight 263.40 g/mol
Exact Mass 263.17077098 g/mol
Topological Polar Surface Area (TPSA) 44.50 Ų
XlogP 7.00
Atomic LogP (AlogP) 5.51
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Farnesyl isothiocyanate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9651 96.51%
Caco-2 + 0.8489 84.89%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4772 47.72%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.9253 92.53%
OATP1B3 inhibitior + 0.9417 94.17%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.5329 53.29%
P-glycoprotein inhibitior - 0.8914 89.14%
P-glycoprotein substrate - 0.9476 94.76%
CYP3A4 substrate - 0.5704 57.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7276 72.76%
CYP3A4 inhibition - 0.8983 89.83%
CYP2C9 inhibition - 0.8214 82.14%
CYP2C19 inhibition - 0.7699 76.99%
CYP2D6 inhibition - 0.8399 83.99%
CYP1A2 inhibition - 0.5422 54.22%
CYP2C8 inhibition - 0.9402 94.02%
CYP inhibitory promiscuity - 0.5854 58.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.5147 51.47%
Eye corrosion + 0.5000 50.00%
Eye irritation - 0.7227 72.27%
Skin irritation + 0.6764 67.64%
Skin corrosion + 0.5420 54.20%
Ames mutagenesis - 0.6378 63.78%
Human Ether-a-go-go-Related Gene inhibition + 0.7176 71.76%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation + 0.5929 59.29%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5635 56.35%
Acute Oral Toxicity (c) III 0.6771 67.71%
Estrogen receptor binding - 0.8161 81.61%
Androgen receptor binding - 0.8668 86.68%
Thyroid receptor binding - 0.5297 52.97%
Glucocorticoid receptor binding - 0.5357 53.57%
Aromatase binding - 0.6586 65.86%
PPAR gamma + 0.6676 66.76%
Honey bee toxicity - 0.6975 69.75%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9825 98.25%

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 95.37% 92.08%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 93.48% 83.57%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 88.91% 95.58%
CHEMBL2581 P07339 Cathepsin D 88.82% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.95% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 85.68% 90.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.48% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 83.43% 94.73%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.58% 93.10%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85642696
LOTUS LTS0197693
wikiData Q104970876