Iberin

Details

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Internal ID fa40c474-cdfa-48af-9b7f-b48ef5908b1c
Taxonomy Organosulfur compounds > Sulfoxides
IUPAC Name 1-isothiocyanato-3-methylsulfinylpropane
SMILES (Canonical) CS(=O)CCCN=C=S
SMILES (Isomeric) CS(=O)CCCN=C=S
InChI InChI=1S/C5H9NOS2/c1-9(7)4-2-3-6-5-8/h2-4H2,1H3
InChI Key LELAOEBVZLPXAZ-UHFFFAOYSA-N
Popularity 44 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9NOS2
Molecular Weight 163.30 g/mol
Exact Mass 163.01255626 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.86
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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505-44-2
3-Methylsulfinylpropyl isothiocyanate
1-Isothiocyanato-3-(methylsulfinyl)propane
1-isothiocyanato-3-methylsulfinylpropane
3-Methylsulphinylpropylisothiocyanate
NSC 321801
3-isothiocyanatopropyl methyl sulfoxide
METHYLSULFINYLPROPYLISOTHIOCYANATE
1-isothiocyanato-3-methanesulfinylpropane
ISOTHIOCYANIC ACID, 3-(METHYLSULFINYL)PROPYL ESTER
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Iberin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9015 90.15%
Caco-2 + 0.8296 82.96%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Lysosomes 0.6521 65.21%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior + 0.9486 94.86%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9088 90.88%
P-glycoprotein inhibitior - 0.9813 98.13%
P-glycoprotein substrate - 0.9089 90.89%
CYP3A4 substrate - 0.5992 59.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7505 75.05%
CYP3A4 inhibition - 0.9681 96.81%
CYP2C9 inhibition - 0.8419 84.19%
CYP2C19 inhibition - 0.7731 77.31%
CYP2D6 inhibition - 0.8943 89.43%
CYP1A2 inhibition - 0.6664 66.64%
CYP2C8 inhibition - 0.9184 91.84%
CYP inhibitory promiscuity - 0.9385 93.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5478 54.78%
Carcinogenicity (trinary) Non-required 0.6596 65.96%
Eye corrosion - 0.6273 62.73%
Eye irritation + 0.8623 86.23%
Skin irritation - 0.5899 58.99%
Skin corrosion - 0.5648 56.48%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7703 77.03%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.5053 50.53%
skin sensitisation - 0.7481 74.81%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6771 67.71%
Acute Oral Toxicity (c) III 0.4555 45.55%
Estrogen receptor binding - 0.7472 74.72%
Androgen receptor binding - 0.9361 93.61%
Thyroid receptor binding - 0.7171 71.71%
Glucocorticoid receptor binding - 0.8563 85.63%
Aromatase binding - 0.7996 79.96%
PPAR gamma - 0.8921 89.21%
Honey bee toxicity - 0.7637 76.37%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity - 0.9245 92.45%

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 89.05% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.04% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.94% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.28% 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.
Arabidopsis thaliana
Brassica oleracea
Lepidium draba

Cross-Links

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PubChem 10455
NPASS NPC305935
LOTUS LTS0079501
wikiData Q27161686