(3aR,8bR)-7-bromo-3-methyl-5,8b-bis(3-methylbut-2-enyl)-2,3a-dihydro-1H-[1]benzofuro[2,3-b]pyrrol-8-amine

Details

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Internal ID 3cbbb543-6c70-43b7-9252-9a3fb5b6d452
Taxonomy Organoheterocyclic compounds > Coumarans
IUPAC Name (3aR,8bR)-7-bromo-3-methyl-5,8b-bis(3-methylbut-2-enyl)-2,3a-dihydro-1H-[1]benzofuro[2,3-b]pyrrol-8-amine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H29BrN2O/c1-13(2)6-7-15-12-16(22)18(23)17-19(15)25-20-21(17,9-8-14(3)4)10-11-24(20)5/h6,8,12,20H,7,9-11,23H2,1-5H3/t20-,21-/m1/s1
InChI Key SQMRGQPMSRIJKQ-NHCUHLMSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H29BrN2O
Molecular Weight 405.40 g/mol
Exact Mass 404.14633 g/mol
Topological Polar Surface Area (TPSA) 38.50 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.19
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3aR,8bR)-7-bromo-3-methyl-5,8b-bis(3-methylbut-2-enyl)-2,3a-dihydro-1H-[1]benzofuro[2,3-b]pyrrol-8-amine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9826 98.26%
Caco-2 + 0.8767 87.67%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.4251 42.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9350 93.50%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.7840 78.40%
P-glycoprotein inhibitior - 0.5203 52.03%
P-glycoprotein substrate + 0.5951 59.51%
CYP3A4 substrate + 0.5943 59.43%
CYP2C9 substrate - 0.6108 61.08%
CYP2D6 substrate + 0.4045 40.45%
CYP3A4 inhibition - 0.5795 57.95%
CYP2C9 inhibition - 0.6390 63.90%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.6087 60.87%
CYP1A2 inhibition - 0.5492 54.92%
CYP2C8 inhibition - 0.8800 88.00%
CYP inhibitory promiscuity + 0.6044 60.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7832 78.32%
Carcinogenicity (trinary) Non-required 0.6222 62.22%
Eye corrosion - 0.9820 98.20%
Eye irritation - 0.9860 98.60%
Skin irritation - 0.7641 76.41%
Skin corrosion - 0.8835 88.35%
Ames mutagenesis + 0.5063 50.63%
Human Ether-a-go-go-Related Gene inhibition + 0.8391 83.91%
Micronuclear + 0.5900 59.00%
Hepatotoxicity + 0.6479 64.79%
skin sensitisation - 0.8179 81.79%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.7999 79.99%
Acute Oral Toxicity (c) III 0.5814 58.14%
Estrogen receptor binding + 0.7442 74.42%
Androgen receptor binding + 0.7093 70.93%
Thyroid receptor binding + 0.7373 73.73%
Glucocorticoid receptor binding + 0.6935 69.35%
Aromatase binding - 0.5086 50.86%
PPAR gamma + 0.8290 82.90%
Honey bee toxicity - 0.8008 80.08%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9918 99.18%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.23% 96.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 94.02% 95.58%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.72% 91.11%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 92.28% 95.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.00% 95.89%
CHEMBL240 Q12809 HERG 89.48% 89.76%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.96% 94.45%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 87.87% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.27% 97.09%
CHEMBL344 Q99705 Melanin-concentrating hormone receptor 1 86.29% 92.50%
CHEMBL3401 O75469 Pregnane X receptor 85.69% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.65% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.39% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.32% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 84.93% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.43% 86.33%
CHEMBL2581 P07339 Cathepsin D 82.85% 98.95%
CHEMBL1871 P10275 Androgen Receptor 82.53% 96.43%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.04% 93.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.59% 95.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.21% 93.04%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.67% 82.38%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.63% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.55% 89.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.16% 100.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.15% 93.40%

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.
There are no matching plants.

Cross-Links

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PubChem 163034721
LOTUS LTS0265112
wikiData Q105258173