(2R)-2-isothiocyanatobutane

Details

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Internal ID 7e6a83ef-ee7f-4af4-b29f-2f6321ffb50a
Taxonomy Organosulfur compounds > Isothiocyanates
IUPAC Name (2R)-2-isothiocyanatobutane
SMILES (Canonical) CCC(C)N=C=S
SMILES (Isomeric) CC[C@@H](C)N=C=S
InChI InChI=1S/C5H9NS/c1-3-5(2)6-4-7/h5H,3H2,1-2H3/t5-/m1/s1
InChI Key TUFJIDJGIQOYFY-RXMQYKEDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9NS
Molecular Weight 115.20 g/mol
Exact Mass 115.04557046 g/mol
Topological Polar Surface Area (TPSA) 44.40 Ų
XlogP 2.80
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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D-2-Butylisothiocyanate
[R,(?)]-2-Isothiocyanatobutane
A826523

2D Structure

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2D Structure of (2R)-2-isothiocyanatobutane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.6648 66.48%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Lysosomes 0.7178 71.78%
OATP2B1 inhibitior - 0.8640 86.40%
OATP1B1 inhibitior + 0.9275 92.75%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9015 90.15%
P-glycoprotein inhibitior - 0.9754 97.54%
P-glycoprotein substrate - 0.9413 94.13%
CYP3A4 substrate - 0.7603 76.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7128 71.28%
CYP3A4 inhibition - 0.9222 92.22%
CYP2C9 inhibition - 0.8986 89.86%
CYP2C19 inhibition - 0.7884 78.84%
CYP2D6 inhibition - 0.7930 79.30%
CYP1A2 inhibition - 0.6136 61.36%
CYP2C8 inhibition - 0.9784 97.84%
CYP inhibitory promiscuity - 0.7715 77.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.5808 58.08%
Eye corrosion + 0.8980 89.80%
Eye irritation + 0.9457 94.57%
Skin irritation + 0.7308 73.08%
Skin corrosion + 0.7528 75.28%
Ames mutagenesis - 0.7124 71.24%
Human Ether-a-go-go-Related Gene inhibition - 0.7456 74.56%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.7838 78.38%
skin sensitisation + 0.6697 66.97%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.6275 62.75%
Acute Oral Toxicity (c) II 0.4941 49.41%
Estrogen receptor binding - 0.8250 82.50%
Androgen receptor binding - 0.9099 90.99%
Thyroid receptor binding - 0.7772 77.72%
Glucocorticoid receptor binding - 0.9460 94.60%
Aromatase binding - 0.8717 87.17%
PPAR gamma - 0.8333 83.33%
Honey bee toxicity - 0.8390 83.90%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity - 0.4523 45.23%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL6007 O75762 Transient receptor potential cation channel subfamily A member 1 680 nM
EC50
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3837 P07711 Cathepsin L 92.29% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.35% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.31% 98.95%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 88.08% 95.58%
CHEMBL2885 P07451 Carbonic anhydrase III 86.42% 87.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.28% 89.34%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.21% 97.25%

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.
Angelica acutiloba
Angelica sinensis
Brassica juncea
Conioselinum anthriscoides
Ligusticum officinale

Cross-Links

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PubChem 5399110
NPASS NPC264111