1-[(E)-2-isothiocyanatoethenyl]-4-methoxybenzene

Details

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Internal ID 6e575be5-60c5-47b0-8fea-309ff3f85bb3
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 1-[(E)-2-isothiocyanatoethenyl]-4-methoxybenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H9NOS/c1-12-10-4-2-9(3-5-10)6-7-11-8-13/h2-7H,1H3/b7-6+
InChI Key IDGIEHXHIVWSHF-VOTSOKGWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H9NOS
Molecular Weight 191.25 g/mol
Exact Mass 191.04048508 g/mol
Topological Polar Surface Area (TPSA) 53.70 Ų
XlogP 3.80
Atomic LogP (AlogP) 2.77
H-Bond Acceptor 3
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 1-[(E)-2-isothiocyanatoethenyl]-4-methoxybenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.8376 83.76%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.5776 57.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9359 93.59%
OATP1B3 inhibitior + 0.9651 96.51%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7802 78.02%
P-glycoprotein inhibitior - 0.9666 96.66%
P-glycoprotein substrate - 0.9619 96.19%
CYP3A4 substrate - 0.5999 59.99%
CYP2C9 substrate + 0.5878 58.78%
CYP2D6 substrate - 0.6666 66.66%
CYP3A4 inhibition - 0.6053 60.53%
CYP2C9 inhibition - 0.8404 84.04%
CYP2C19 inhibition - 0.5642 56.42%
CYP2D6 inhibition - 0.9054 90.54%
CYP1A2 inhibition + 0.7961 79.61%
CYP2C8 inhibition - 0.7323 73.23%
CYP inhibitory promiscuity + 0.8037 80.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5820 58.20%
Carcinogenicity (trinary) Non-required 0.5818 58.18%
Eye corrosion - 0.6229 62.29%
Eye irritation + 0.9272 92.72%
Skin irritation + 0.5129 51.29%
Skin corrosion - 0.7112 71.12%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5588 55.88%
Micronuclear - 0.6219 62.19%
Hepatotoxicity - 0.5217 52.17%
skin sensitisation + 0.5453 54.53%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.5994 59.94%
Acute Oral Toxicity (c) III 0.6413 64.13%
Estrogen receptor binding + 0.5310 53.10%
Androgen receptor binding + 0.5776 57.76%
Thyroid receptor binding - 0.7319 73.19%
Glucocorticoid receptor binding - 0.6408 64.08%
Aromatase binding - 0.5641 56.41%
PPAR gamma - 0.7622 76.22%
Honey bee toxicity - 0.8676 86.76%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.8800 88.00%
Fish aquatic toxicity + 0.7320 73.20%

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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 97.13% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.56% 91.11%
CHEMBL4208 P20618 Proteasome component C5 90.53% 90.00%
CHEMBL2487 P05067 Beta amyloid A4 protein 89.27% 96.74%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.10% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.46% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 84.69% 93.31%
CHEMBL2039 P27338 Monoamine oxidase B 84.26% 92.51%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.18% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.83% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.09% 93.99%
CHEMBL1907599 P05556 Integrin alpha-4/beta-1 82.01% 92.86%
CHEMBL1951 P21397 Monoamine oxidase A 80.77% 91.49%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.49% 90.24%

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.
Corsinia coriandrina

Cross-Links

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PubChem 11298450
LOTUS LTS0082074
wikiData Q105111332