3-Butenyl isothiocyanate

Details

Top
Internal ID 9531a76a-d7d8-40ba-a4db-4d3dac4f558c
Taxonomy Organosulfur compounds > Isothiocyanates
IUPAC Name 4-isothiocyanatobut-1-ene
SMILES (Canonical) C=CCCN=C=S
SMILES (Isomeric) C=CCCN=C=S
InChI InChI=1S/C5H7NS/c1-2-3-4-6-5-7/h2H,1,3-4H2
InChI Key SKIHGKNFJKJXPX-UHFFFAOYSA-N
Popularity 113 references in papers

Physical and Chemical Properties

Top
Molecular Formula C5H7NS
Molecular Weight 113.18 g/mol
Exact Mass 113.02992040 g/mol
Topological Polar Surface Area (TPSA) 44.40 Ų
XlogP 2.70
Atomic LogP (AlogP) 1.67
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
3386-97-8
4-isothiocyanatobut-1-ene
Isothiocyanic Acid 3-Buten-1-yl Ester
1-Butene, 4-isothiocyanato-
3-Buten-1-yl Isothiocyanate
Isothiocyanic acid, 3-butenyl ester
4-Isothiocyanato-1-butene
But-3-enyl isothiocyanate
UNII-13O98H1EW1
CHEMBL3593942
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 3-Butenyl isothiocyanate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9525 95.25%
Caco-2 + 0.7199 71.99%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.5203 52.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9446 94.46%
OATP1B3 inhibitior + 0.9477 94.77%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9558 95.58%
P-glycoprotein inhibitior - 0.9819 98.19%
P-glycoprotein substrate - 0.9775 97.75%
CYP3A4 substrate - 0.6921 69.21%
CYP2C9 substrate - 0.8142 81.42%
CYP2D6 substrate - 0.6874 68.74%
CYP3A4 inhibition - 0.8856 88.56%
CYP2C9 inhibition - 0.8596 85.96%
CYP2C19 inhibition - 0.7437 74.37%
CYP2D6 inhibition - 0.8764 87.64%
CYP1A2 inhibition + 0.5881 58.81%
CYP2C8 inhibition - 0.9477 94.77%
CYP inhibitory promiscuity - 0.5846 58.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.4747 47.47%
Eye corrosion + 0.9487 94.87%
Eye irritation + 0.9828 98.28%
Skin irritation + 0.7882 78.82%
Skin corrosion + 0.8552 85.52%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6587 65.87%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.5394 53.94%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.7159 71.59%
Acute Oral Toxicity (c) II 0.6332 63.32%
Estrogen receptor binding - 0.8119 81.19%
Androgen receptor binding - 0.9468 94.68%
Thyroid receptor binding - 0.7563 75.63%
Glucocorticoid receptor binding - 0.7201 72.01%
Aromatase binding - 0.7887 78.87%
PPAR gamma - 0.8183 81.83%
Honey bee toxicity + 0.5595 55.95%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity - 0.5120 51.20%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL6007 O75762 Transient receptor potential cation channel subfamily A member 1 360 nM
360 nM
EC50
EC50
PMID: 26263397
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 95.77% 83.57%
CHEMBL240 Q12809 HERG 86.50% 89.76%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.47% 89.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.54% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.54% 96.00%

Plants that contains it

Top
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.
Alyssum desertorum
Brassica juncea
Brassica napus
Brassica oleracea
Brassica rapa
Diplotaxis harra
Eutrema japonicum
Sinapis alba

Cross-Links

Top
PubChem 76922
NPASS NPC27723
ChEMBL CHEMBL3593942
LOTUS LTS0097937
wikiData Q27251535