Brachyamide A

Details

Top
Internal ID ae489e85-96da-4943-a3f9-ce8bc4a03cf1
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name (2E,4E,12E)-13-(1,3-benzodioxol-5-yl)-1-pyrrolidin-1-yltrideca-2,4,12-trien-1-one
SMILES (Canonical) C1CCN(C1)C(=O)C=CC=CCCCCCCC=CC2=CC3=C(C=C2)OCO3
SMILES (Isomeric) C1CCN(C1)C(=O)/C=C/C=C/CCCCCC/C=C/C2=CC3=C(C=C2)OCO3
InChI InChI=1S/C24H31NO3/c26-24(25-17-11-12-18-25)14-10-8-6-4-2-1-3-5-7-9-13-21-15-16-22-23(19-21)28-20-27-22/h6,8-10,13-16,19H,1-5,7,11-12,17-18,20H2/b8-6+,13-9+,14-10+
InChI Key CLVADUMCAXEPEK-NQWJBOIKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H31NO3
Molecular Weight 381.50 g/mol
Exact Mass 381.23039385 g/mol
Topological Polar Surface Area (TPSA) 38.80 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.50
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Brachyamide A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 - 0.6425 64.25%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6814 68.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9218 92.18%
OATP1B3 inhibitior + 0.9484 94.84%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.8755 87.55%
P-glycoprotein inhibitior + 0.7380 73.80%
P-glycoprotein substrate - 0.8088 80.88%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition + 0.5787 57.87%
CYP2C9 inhibition - 0.8848 88.48%
CYP2C19 inhibition - 0.5405 54.05%
CYP2D6 inhibition + 0.6816 68.16%
CYP1A2 inhibition + 0.8675 86.75%
CYP2C8 inhibition - 0.8090 80.90%
CYP inhibitory promiscuity + 0.6580 65.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5667 56.67%
Eye corrosion - 0.9814 98.14%
Eye irritation - 0.7837 78.37%
Skin irritation - 0.6982 69.82%
Skin corrosion - 0.7971 79.71%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8705 87.05%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.6908 69.08%
skin sensitisation - 0.8093 80.93%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.8337 83.37%
Acute Oral Toxicity (c) III 0.7691 76.91%
Estrogen receptor binding + 0.8225 82.25%
Androgen receptor binding + 0.9008 90.08%
Thyroid receptor binding + 0.5261 52.61%
Glucocorticoid receptor binding + 0.6141 61.41%
Aromatase binding + 0.5887 58.87%
PPAR gamma - 0.5459 54.59%
Honey bee toxicity - 0.9317 93.17%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5686 56.86%
Fish aquatic toxicity + 0.8269 82.69%

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 96.56% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.66% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.26% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.63% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.13% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.83% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.92% 96.77%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.90% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.08% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.54% 89.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.51% 91.71%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 86.70% 90.24%
CHEMBL4208 P20618 Proteasome component C5 85.06% 90.00%
CHEMBL230 P35354 Cyclooxygenase-2 83.71% 89.63%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.10% 90.71%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 82.82% 96.25%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.62% 89.62%

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.
Piper mullesua
Piper nigrum

Cross-Links

Top
PubChem 14162525
NPASS NPC33991
LOTUS LTS0228827
wikiData Q104963985