Isothiocyanatocyclopropane

Details

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Internal ID 2521c1d9-2e56-4bfd-b247-21834b9ad773
Taxonomy Organosulfur compounds > Isothiocyanates
IUPAC Name isothiocyanatocyclopropane
SMILES (Canonical) C1CC1N=C=S
SMILES (Isomeric) C1CC1N=C=S
InChI InChI=1S/C4H5NS/c6-3-5-4-1-2-4/h4H,1-2H2
InChI Key JGFBQFKZKSSODQ-UHFFFAOYSA-N
Popularity 13 references in papers

Physical and Chemical Properties

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Molecular Formula C4H5NS
Molecular Weight 99.16 g/mol
Exact Mass 99.01427034 g/mol
Topological Polar Surface Area (TPSA) 44.40 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.25
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Isothiocyanatocyclopropane
56601-42-4
Cyclopropane, isothiocyanato-
isothiocyanato-cyclopropane
EINECS 260-278-6
MFCD00040874
Methylbutyrate
cyclopropyl iso-thiocyanate
Isothiocyanatocyclopropane #
CHEBI:88382
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isothiocyanatocyclopropane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9746 97.46%
Caco-2 + 0.6393 63.93%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.6992 69.92%
OATP2B1 inhibitior - 0.8658 86.58%
OATP1B1 inhibitior + 0.9786 97.86%
OATP1B3 inhibitior + 0.9510 95.10%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9495 94.95%
P-glycoprotein inhibitior - 0.9832 98.32%
P-glycoprotein substrate - 0.9847 98.47%
CYP3A4 substrate - 0.7050 70.50%
CYP2C9 substrate - 0.8132 81.32%
CYP2D6 substrate - 0.6679 66.79%
CYP3A4 inhibition - 0.9531 95.31%
CYP2C9 inhibition - 0.9239 92.39%
CYP2C19 inhibition - 0.6481 64.81%
CYP2D6 inhibition - 0.9183 91.83%
CYP1A2 inhibition + 0.5794 57.94%
CYP2C8 inhibition - 0.9540 95.40%
CYP inhibitory promiscuity - 0.7361 73.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6203 62.03%
Eye corrosion + 0.9568 95.68%
Eye irritation + 0.9498 94.98%
Skin irritation + 0.8024 80.24%
Skin corrosion + 0.8873 88.73%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7052 70.52%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation + 0.5232 52.32%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.6018 60.18%
Acute Oral Toxicity (c) II 0.8327 83.27%
Estrogen receptor binding - 0.7565 75.65%
Androgen receptor binding - 0.9494 94.94%
Thyroid receptor binding - 0.7646 76.46%
Glucocorticoid receptor binding - 0.9186 91.86%
Aromatase binding - 0.8716 87.16%
PPAR gamma - 0.8401 84.01%
Honey bee toxicity + 0.5451 54.51%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity - 0.6917 69.17%

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
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 90.39% 95.58%
CHEMBL3837 P07711 Cathepsin L 87.87% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.88% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.46% 99.18%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.51% 91.11%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 80.01% 83.57%

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 92463
NPASS NPC64663