3-(1-Isothiocyanato-2-methylprop-2-enyl)-4,7a-dimethyl-1,2,3,3a,4,5,6,7-octahydroindene

Details

Top
Internal ID 3a086e5e-b5de-4b9a-ace1-1e70a0a5d831
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3-(1-isothiocyanato-2-methylprop-2-enyl)-4,7a-dimethyl-1,2,3,3a,4,5,6,7-octahydroindene
SMILES (Canonical) CC1CCCC2(C1C(CC2)C(C(=C)C)N=C=S)C
SMILES (Isomeric) CC1CCCC2(C1C(CC2)C(C(=C)C)N=C=S)C
InChI InChI=1S/C16H25NS/c1-11(2)15(17-10-18)13-7-9-16(4)8-5-6-12(3)14(13)16/h12-15H,1,5-9H2,2-4H3
InChI Key DYINHGJSKDCGLB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H25NS
Molecular Weight 263.40 g/mol
Exact Mass 263.17077098 g/mol
Topological Polar Surface Area (TPSA) 44.50 Ų
XlogP 7.10
Atomic LogP (AlogP) 4.89
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-(1-Isothiocyanato-2-methylprop-2-enyl)-4,7a-dimethyl-1,2,3,3a,4,5,6,7-octahydroindene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9865 98.65%
Caco-2 + 0.6274 62.74%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.7273 72.73%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.9331 93.31%
OATP1B3 inhibitior + 0.9346 93.46%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.6400 64.00%
P-glycoprotein inhibitior - 0.8697 86.97%
P-glycoprotein substrate - 0.8045 80.45%
CYP3A4 substrate + 0.5945 59.45%
CYP2C9 substrate - 0.7657 76.57%
CYP2D6 substrate - 0.7195 71.95%
CYP3A4 inhibition - 0.6452 64.52%
CYP2C9 inhibition - 0.7410 74.10%
CYP2C19 inhibition - 0.6099 60.99%
CYP2D6 inhibition - 0.8764 87.64%
CYP1A2 inhibition - 0.6287 62.87%
CYP2C8 inhibition - 0.6900 69.00%
CYP inhibitory promiscuity + 0.5528 55.28%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.5091 50.91%
Eye corrosion - 0.9274 92.74%
Eye irritation - 0.8191 81.91%
Skin irritation - 0.5606 56.06%
Skin corrosion - 0.8524 85.24%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5722 57.22%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.5057 50.57%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5106 51.06%
Acute Oral Toxicity (c) III 0.6537 65.37%
Estrogen receptor binding - 0.5223 52.23%
Androgen receptor binding + 0.6476 64.76%
Thyroid receptor binding + 0.5527 55.27%
Glucocorticoid receptor binding - 0.5201 52.01%
Aromatase binding - 0.6619 66.19%
PPAR gamma - 0.6230 62.30%
Honey bee toxicity - 0.6147 61.47%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9968 99.68%

Targets

Top

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 95.95% 95.58%
CHEMBL1951 P21397 Monoamine oxidase A 95.58% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.20% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.33% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.26% 97.25%
CHEMBL3837 P07711 Cathepsin L 89.20% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.21% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.97% 82.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.76% 92.94%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 84.19% 91.03%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.15% 100.00%
CHEMBL2581 P07339 Cathepsin D 83.64% 98.95%
CHEMBL1871 P10275 Androgen Receptor 82.55% 96.43%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.48% 99.18%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 81.92% 97.31%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 81.91% 96.38%
CHEMBL259 P32245 Melanocortin receptor 4 81.85% 95.38%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.66% 93.04%
CHEMBL5600 P27448 Serine/threonine-protein kinase c-TAK1 81.62% 88.81%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.46% 95.89%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 73836236
LOTUS LTS0174141
wikiData Q104991379