5-Hexenyl isothiocyanate

Details

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Internal ID 5f620dbf-d4ab-499e-b844-d77cd4319794
Taxonomy Organosulfur compounds > Isothiocyanates
IUPAC Name 6-isothiocyanatohex-1-ene
SMILES (Canonical) C=CCCCCN=C=S
SMILES (Isomeric) C=CCCCCN=C=S
InChI InChI=1S/C7H11NS/c1-2-3-4-5-6-8-7-9/h2H,1,3-6H2
InChI Key WRFHVMFZOJHYGN-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C7H11NS
Molecular Weight 141.24 g/mol
Exact Mass 141.06122053 g/mol
Topological Polar Surface Area (TPSA) 44.40 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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6-isothiocyanatohex-1-ene
49776-81-0
5-HEXEN-1-YL ISOTHIOCYANATE
6-Isothiocyanato-1-hexene
1-Hexene, 6-isothiocyanato-
FEMA No. 4421
G1Q3G6DQPO
CHEMBL3593944
UNII-G1Q3G6DQPO
5-Hexenyl isothiocyanate [FIFH]
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-Hexenyl isothiocyanate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9422 94.22%
Caco-2 + 0.8624 86.24%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.4815 48.15%
OATP2B1 inhibitior - 0.8648 86.48%
OATP1B1 inhibitior + 0.9379 93.79%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9521 95.21%
P-glycoprotein inhibitior - 0.9828 98.28%
P-glycoprotein substrate - 0.9499 94.99%
CYP3A4 substrate - 0.6446 64.46%
CYP2C9 substrate - 0.8142 81.42%
CYP2D6 substrate - 0.6874 68.74%
CYP3A4 inhibition - 0.8519 85.19%
CYP2C9 inhibition - 0.8501 85.01%
CYP2C19 inhibition - 0.7110 71.10%
CYP2D6 inhibition - 0.8676 86.76%
CYP1A2 inhibition + 0.6183 61.83%
CYP2C8 inhibition - 0.8763 87.63%
CYP inhibitory promiscuity - 0.5098 50.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.4667 46.67%
Eye corrosion + 0.9196 91.96%
Eye irritation + 0.9466 94.66%
Skin irritation + 0.7745 77.45%
Skin corrosion + 0.8188 81.88%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6530 65.30%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.5463 54.63%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.6006 60.06%
Acute Oral Toxicity (c) II 0.5134 51.34%
Estrogen receptor binding - 0.7894 78.94%
Androgen receptor binding - 0.9492 94.92%
Thyroid receptor binding - 0.7805 78.05%
Glucocorticoid receptor binding - 0.7931 79.31%
Aromatase binding - 0.7785 77.85%
PPAR gamma - 0.7658 76.58%
Honey bee toxicity - 0.5114 51.14%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.7236 72.36%

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
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 93.24% 83.57%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.72% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.18% 96.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.27% 89.34%

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.
Eutrema japonicum

Cross-Links

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PubChem 184852
LOTUS LTS0036716
wikiData Q27278609