4-Isothiocyanato-3-methylbut-1-ene

Details

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Internal ID 81c7da84-356d-4d08-a8c1-f2fc25ff5978
Taxonomy Organosulfur compounds > Isothiocyanates
IUPAC Name 4-isothiocyanato-3-methylbut-1-ene
SMILES (Canonical) CC(CN=C=S)C=C
SMILES (Isomeric) CC(CN=C=S)C=C
InChI InChI=1S/C6H9NS/c1-3-6(2)4-7-5-8/h3,6H,1,4H2,2H3
InChI Key ISVIEXMVIMLCSG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H9NS
Molecular Weight 127.21 g/mol
Exact Mass 127.04557046 g/mol
Topological Polar Surface Area (TPSA) 44.40 Ų
XlogP 3.00
Atomic LogP (AlogP) 1.91
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Isothiocyanato-3-methylbut-1-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9635 96.35%
Caco-2 + 0.5279 52.79%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.5799 57.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9482 94.82%
OATP1B3 inhibitior + 0.9484 94.84%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9367 93.67%
P-glycoprotein inhibitior - 0.9767 97.67%
P-glycoprotein substrate - 0.9536 95.36%
CYP3A4 substrate - 0.7071 70.71%
CYP2C9 substrate - 0.7656 76.56%
CYP2D6 substrate - 0.7754 77.54%
CYP3A4 inhibition - 0.8060 80.60%
CYP2C9 inhibition - 0.8747 87.47%
CYP2C19 inhibition - 0.7864 78.64%
CYP2D6 inhibition - 0.8625 86.25%
CYP1A2 inhibition - 0.5110 51.10%
CYP2C8 inhibition - 0.9718 97.18%
CYP inhibitory promiscuity - 0.6674 66.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.5196 51.96%
Eye corrosion + 0.9532 95.32%
Eye irritation + 0.9896 98.96%
Skin irritation + 0.8139 81.39%
Skin corrosion + 0.8953 89.53%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7195 71.95%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.7463 74.63%
skin sensitisation + 0.6502 65.02%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.5821 58.21%
Acute Oral Toxicity (c) II 0.4873 48.73%
Estrogen receptor binding - 0.8378 83.78%
Androgen receptor binding - 0.9060 90.60%
Thyroid receptor binding - 0.7673 76.73%
Glucocorticoid receptor binding - 0.6403 64.03%
Aromatase binding - 0.8519 85.19%
PPAR gamma - 0.8425 84.25%
Honey bee toxicity - 0.6724 67.24%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8552 85.52%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.11% 89.34%
CHEMBL2885 P07451 Carbonic anhydrase III 88.91% 87.45%
CHEMBL3837 P07711 Cathepsin L 87.78% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.93% 96.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 84.84% 95.58%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.75% 96.00%
CHEMBL2581 P07339 Cathepsin D 81.70% 98.95%

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.
Diplotaxis harra

Cross-Links

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PubChem 91751214
LOTUS LTS0177981
wikiData Q104667212