1-Isothiocyanato-3-methylbutane

Details

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Internal ID bd707f0f-341b-41ef-b5b0-2644c1f0d209
Taxonomy Organosulfur compounds > Isothiocyanates
IUPAC Name 1-isothiocyanato-3-methylbutane
SMILES (Canonical) CC(C)CCN=C=S
SMILES (Isomeric) CC(C)CCN=C=S
InChI InChI=1S/C6H11NS/c1-6(2)3-4-7-5-8/h6H,3-4H2,1-2H3
InChI Key JATNWMBUDXLMEO-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NS
Molecular Weight 129.23 g/mol
Exact Mass 129.06122053 g/mol
Topological Polar Surface Area (TPSA) 44.40 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.14
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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1-Isothiocyanato-3-methylbutane
628-03-5
isoamyl isothiocyanate
Butane, 1-isothiocyanato-3-methyl-
UNII-HLP916O2C9
HLP916O2C9
3-methylbutylisothiocyanate
Isoamylisothiocyanat
ISOPENTYL ISOTHIOCYANATE
SCHEMBL1679686
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Isothiocyanato-3-methylbutane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9737 97.37%
Caco-2 + 0.7369 73.69%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.6663 66.63%
OATP2B1 inhibitior - 0.8629 86.29%
OATP1B1 inhibitior + 0.9578 95.78%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9698 96.98%
P-glycoprotein inhibitior - 0.9862 98.62%
P-glycoprotein substrate - 0.9221 92.21%
CYP3A4 substrate - 0.6921 69.21%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7167 71.67%
CYP3A4 inhibition - 0.9667 96.67%
CYP2C9 inhibition - 0.8979 89.79%
CYP2C19 inhibition - 0.8166 81.66%
CYP2D6 inhibition - 0.8493 84.93%
CYP1A2 inhibition - 0.5520 55.20%
CYP2C8 inhibition - 0.9892 98.92%
CYP inhibitory promiscuity - 0.8925 89.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6994 69.94%
Eye corrosion + 0.9625 96.25%
Eye irritation + 0.9912 99.12%
Skin irritation + 0.7602 76.02%
Skin corrosion + 0.8553 85.53%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7598 75.98%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6713 67.13%
skin sensitisation + 0.5736 57.36%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.5385 53.85%
Acute Oral Toxicity (c) III 0.4736 47.36%
Estrogen receptor binding - 0.8597 85.97%
Androgen receptor binding - 0.9158 91.58%
Thyroid receptor binding - 0.6536 65.36%
Glucocorticoid receptor binding - 0.9051 90.51%
Aromatase binding - 0.7962 79.62%
PPAR gamma - 0.8907 89.07%
Honey bee toxicity - 0.8210 82.10%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity - 0.4143 41.43%

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
CHEMBL2581 P07339 Cathepsin D 88.02% 98.95%
CHEMBL3837 P07711 Cathepsin L 87.38% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.74% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.60% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 86.55% 93.31%
CHEMBL2885 P07451 Carbonic anhydrase III 86.27% 87.45%
CHEMBL230 P35354 Cyclooxygenase-2 80.68% 89.63%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.67% 96.61%

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.
Brassica juncea
Sinapis alba

Cross-Links

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PubChem 79086
NPASS NPC173003