Benzastatin G

Details

Top
Internal ID 87f61ea4-60ca-4e1e-b09d-ba471a6eeaf3
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolines
IUPAC Name (2R)-2-(2-hydroxy-6-methylhept-5-en-2-yl)-2,3-dihydro-1H-indole-5-carboxamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H24N2O2/c1-11(2)5-4-8-17(3,21)15-10-13-9-12(16(18)20)6-7-14(13)19-15/h5-7,9,15,19,21H,4,8,10H2,1-3H3,(H2,18,20)/t15-,17?/m1/s1
InChI Key ODYCYXKNGGGAMF-LDCVWXEPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C17H24N2O2
Molecular Weight 288.40 g/mol
Exact Mass 288.183778013 g/mol
Topological Polar Surface Area (TPSA) 75.40 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.62
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

Top
(2R)-2-(2-hydroxy-6-methylhept-5-en-2-yl)-2,3-dihydro-1H-indole-5-carboxamide
RefChem:117178
SCHEMBL29885793
CHEBI:198398

2D Structure

Top
2D Structure of Benzastatin G

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 - 0.6214 62.14%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5327 53.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9241 92.41%
OATP1B3 inhibitior + 0.9397 93.97%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.4918 49.18%
P-glycoprotein inhibitior - 0.8688 86.88%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.5065 50.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7469 74.69%
CYP3A4 inhibition - 0.5898 58.98%
CYP2C9 inhibition - 0.6234 62.34%
CYP2C19 inhibition - 0.5233 52.33%
CYP2D6 inhibition - 0.8380 83.80%
CYP1A2 inhibition - 0.6973 69.73%
CYP2C8 inhibition - 0.7317 73.17%
CYP inhibitory promiscuity + 0.5504 55.04%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6061 60.61%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.9789 97.89%
Skin irritation - 0.7749 77.49%
Skin corrosion - 0.9202 92.02%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6606 66.06%
Micronuclear - 0.5100 51.00%
Hepatotoxicity - 0.5447 54.47%
skin sensitisation - 0.8271 82.71%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.8464 84.64%
Acute Oral Toxicity (c) III 0.5912 59.12%
Estrogen receptor binding + 0.6449 64.49%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.5962 59.62%
Glucocorticoid receptor binding - 0.4783 47.83%
Aromatase binding - 0.5460 54.60%
PPAR gamma + 0.7537 75.37%
Honey bee toxicity - 0.9092 90.92%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5752 57.52%
Fish aquatic toxicity + 0.9193 91.93%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.77% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.10% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.86% 97.25%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 94.49% 96.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.08% 97.09%
CHEMBL2581 P07339 Cathepsin D 93.70% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.26% 86.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 93.04% 89.34%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.93% 97.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.61% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.69% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.63% 99.17%
CHEMBL236 P41143 Delta opioid receptor 87.02% 99.35%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.84% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 85.49% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.24% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.89% 90.00%
CHEMBL3437 Q16853 Amine oxidase, copper containing 84.68% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.50% 92.94%
CHEMBL4581 P52732 Kinesin-like protein 1 82.07% 93.18%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.69% 90.71%

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 139583365
LOTUS LTS0118618
wikiData Q75059646