Erucin

Details

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Internal ID 84b253af-ebae-4536-a2fd-be5737333cab
Taxonomy Organosulfur compounds > Isothiocyanates
IUPAC Name 1-isothiocyanato-4-methylsulfanylbutane
SMILES (Canonical) CSCCCCN=C=S
SMILES (Isomeric) CSCCCCN=C=S
InChI InChI=1S/C6H11NS2/c1-9-5-3-2-4-7-6-8/h2-5H2,1H3
InChI Key IHQDGXUYTSZGOG-UHFFFAOYSA-N
Popularity 104 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NS2
Molecular Weight 161.30 g/mol
Exact Mass 161.03329170 g/mol
Topological Polar Surface Area (TPSA) 69.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.23
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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4430-36-8
4-methylthiobutyl isothiocyanate
4-(Methylthio)butyl isothiocyanate
CCRIS 9056
(4-isothiocyanatobutyl)(methyl)sulfane
1-isothiocyanato-4-methylsulfanylbutane
4-(METHYLTHIOL)-1-(ISOTHIOCYANATO)BUTANE
CTE370DL3U
1-isothiocyanato-4-(methylsulfanyl)butane
Butane, 1-isothiocyanato-4-(methylthio)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Erucin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9135 91.35%
Caco-2 + 0.8921 89.21%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.7622 76.22%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.9383 93.83%
OATP1B3 inhibitior + 0.9463 94.63%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.9717 97.17%
P-glycoprotein inhibitior - 0.9844 98.44%
P-glycoprotein substrate - 0.8568 85.68%
CYP3A4 substrate - 0.6250 62.50%
CYP2C9 substrate - 0.8092 80.92%
CYP2D6 substrate - 0.7252 72.52%
CYP3A4 inhibition - 0.9622 96.22%
CYP2C9 inhibition - 0.8905 89.05%
CYP2C19 inhibition - 0.8056 80.56%
CYP2D6 inhibition - 0.8659 86.59%
CYP1A2 inhibition - 0.5540 55.40%
CYP2C8 inhibition - 0.9035 90.35%
CYP inhibitory promiscuity - 0.9179 91.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5721 57.21%
Eye corrosion + 0.8127 81.27%
Eye irritation + 0.8382 83.82%
Skin irritation + 0.7069 70.69%
Skin corrosion + 0.8294 82.94%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6337 63.37%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.5801 58.01%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.8257 82.57%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.7184 71.84%
Acute Oral Toxicity (c) III 0.4493 44.93%
Estrogen receptor binding - 0.6956 69.56%
Androgen receptor binding - 0.9443 94.43%
Thyroid receptor binding - 0.5984 59.84%
Glucocorticoid receptor binding - 0.8588 85.88%
Aromatase binding - 0.8223 82.23%
PPAR gamma - 0.8409 84.09%
Honey bee toxicity - 0.7867 78.67%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.5664 56.64%

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 1 420 nM
EC50
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 91.04% 83.57%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.70% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.68% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.09% 98.95%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 82.52% 87.16%
CHEMBL2885 P07451 Carbonic anhydrase III 82.27% 87.45%

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 napus
Brassica oleracea
Cleome chrysantha

Cross-Links

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PubChem 78160
LOTUS LTS0016500
wikiData Q27275769