Thiiranepropanenitrile

Details

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Internal ID 9fcc6f56-c03b-4983-84ba-63d1a98d63d4
Taxonomy Organoheterocyclic compounds > Thiiranes
IUPAC Name 3-(thiiran-2-yl)propanenitrile
SMILES (Canonical) C1C(S1)CCC#N
SMILES (Isomeric) C1C(S1)CCC#N
InChI InChI=1S/C5H7NS/c6-3-1-2-5-4-7-5/h5H,1-2,4H2
InChI Key ZAGXORSINWAUSP-UHFFFAOYSA-N
Popularity 18 references in papers

Physical and Chemical Properties

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Molecular Formula C5H7NS
Molecular Weight 113.18 g/mol
Exact Mass 113.02992040 g/mol
Topological Polar Surface Area (TPSA) 49.10 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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3-(thiiran-2-yl)propanenitrile
1-Cyano-3,4-epithiobutane
4,5-Epithiovaleronitrile
CYANO-3,4-EPITHIOBUTANE
54096-45-6
Valeronitrile, 4,5-epithio-
NSC 322064
BRN 1362236
5-18-06-00016 (Beilstein Handbook Reference)
76786-81-7
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Thiiranepropanenitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9841 98.41%
Caco-2 + 0.6049 60.49%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.4262 42.62%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.9672 96.72%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9387 93.87%
P-glycoprotein inhibitior - 0.9886 98.86%
P-glycoprotein substrate - 0.9608 96.08%
CYP3A4 substrate - 0.6456 64.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7254 72.54%
CYP3A4 inhibition - 0.8584 85.84%
CYP2C9 inhibition - 0.6852 68.52%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.7951 79.51%
CYP1A2 inhibition + 0.5903 59.03%
CYP2C8 inhibition - 0.9551 95.51%
CYP inhibitory promiscuity + 0.5974 59.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.6118 61.18%
Eye corrosion + 0.8670 86.70%
Eye irritation + 0.9757 97.57%
Skin irritation + 0.7203 72.03%
Skin corrosion + 0.5643 56.43%
Ames mutagenesis - 0.7032 70.32%
Human Ether-a-go-go-Related Gene inhibition - 0.6474 64.74%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.7105 71.05%
skin sensitisation - 0.5464 54.64%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.7064 70.64%
Acute Oral Toxicity (c) II 0.4190 41.90%
Estrogen receptor binding - 0.8776 87.76%
Androgen receptor binding - 0.9152 91.52%
Thyroid receptor binding - 0.7708 77.08%
Glucocorticoid receptor binding - 0.7538 75.38%
Aromatase binding - 0.8421 84.21%
PPAR gamma - 0.8322 83.22%
Honey bee toxicity + 0.5897 58.97%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity - 0.4090 40.90%

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
CHEMBL3529 Q14164 Inhibitor of nuclear factor kappa B kinase epsilon subunit 91.38% 98.19%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.90% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.27% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 88.98% 95.93%
CHEMBL1871 P10275 Androgen Receptor 85.73% 96.43%
CHEMBL221 P23219 Cyclooxygenase-1 84.18% 90.17%
CHEMBL2835 P23458 Tyrosine-protein kinase JAK1 83.58% 98.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.64% 91.11%

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
Brassica napus
Brassica rapa

Cross-Links

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PubChem 100582
NPASS NPC291466
LOTUS LTS0198039
wikiData Q82990601