Isopropyl Isothiocyanate

Details

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Internal ID 10e197bd-cfd6-43f4-b5ff-7c10ec8f235e
Taxonomy Organosulfur compounds > Isothiocyanates
IUPAC Name 2-isothiocyanatopropane
SMILES (Canonical) CC(C)N=C=S
SMILES (Isomeric) CC(C)N=C=S
InChI InChI=1S/C4H7NS/c1-4(2)5-3-6/h4H,1-2H3
InChI Key VHBFEIBMZHEWSX-UHFFFAOYSA-N
Popularity 91 references in papers

Physical and Chemical Properties

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Molecular Formula C4H7NS
Molecular Weight 101.17 g/mol
Exact Mass 101.02992040 g/mol
Topological Polar Surface Area (TPSA) 44.40 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.50
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2253-73-8
2-Isothiocyanatopropane
isopropylisothiocyanate
Isothiocyanic Acid Isopropyl Ester
Propane, 2-isothiocyanato-
Putranjivine
Isothiocyanic acid, isopropyl ester
UNII-46561PKP9T
46561PKP9T
EINECS 218-851-3
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isopropyl Isothiocyanate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 - 0.5357 53.57%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.7081 70.81%
OATP2B1 inhibitior - 0.8700 87.00%
OATP1B1 inhibitior + 0.9690 96.90%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9346 93.46%
P-glycoprotein inhibitior - 0.9735 97.35%
P-glycoprotein substrate - 0.9741 97.41%
CYP3A4 substrate - 0.7620 76.20%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7630 76.30%
CYP3A4 inhibition - 0.9509 95.09%
CYP2C9 inhibition - 0.9278 92.78%
CYP2C19 inhibition - 0.8042 80.42%
CYP2D6 inhibition - 0.8712 87.12%
CYP1A2 inhibition - 0.7750 77.50%
CYP2C8 inhibition - 0.9932 99.32%
CYP inhibitory promiscuity - 0.8659 86.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.5770 57.70%
Eye corrosion + 0.9729 97.29%
Eye irritation + 0.9573 95.73%
Skin irritation + 0.8218 82.18%
Skin corrosion + 0.9196 91.96%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7397 73.97%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.8677 86.77%
skin sensitisation + 0.6438 64.38%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.6752 67.52%
Acute Oral Toxicity (c) II 0.5257 52.57%
Estrogen receptor binding - 0.9395 93.95%
Androgen receptor binding - 0.9401 94.01%
Thyroid receptor binding - 0.8403 84.03%
Glucocorticoid receptor binding - 0.9398 93.98%
Aromatase binding - 0.8927 89.27%
PPAR gamma - 0.9082 90.82%
Honey bee toxicity - 0.7088 70.88%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity - 0.5430 54.30%

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 1 530 nM
530 nM
EC50
EC50
PMID: 26263397
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 90.50% 83.57%
CHEMBL3837 P07711 Cathepsin L 87.21% 96.61%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 82.50% 95.58%
CHEMBL2885 P07451 Carbonic anhydrase III 81.95% 87.45%
CHEMBL2581 P07339 Cathepsin D 81.07% 98.95%

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
Erucaria microcarpa

Cross-Links

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PubChem 75263
NPASS NPC266347
ChEMBL CHEMBL2208211
LOTUS LTS0191234
wikiData Q27258900