Amoenamide A

Details

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Internal ID 5f70ce3d-2a65-4c5c-927c-611843e22204
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name N-[6-[2-[(3S,8aS)-1,4-dioxo-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazin-3-yl]acetyl]-2,2-dimethylchromen-5-yl]-2,2-dimethylbut-3-enamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H31N3O5/c1-6-25(2,3)24(33)28-21-15(9-10-20-16(21)11-12-26(4,5)34-20)19(30)14-17-23(32)29-13-7-8-18(29)22(31)27-17/h6,9-12,17-18H,1,7-8,13-14H2,2-5H3,(H,27,31)(H,28,33)/t17-,18-/m0/s1
InChI Key CQIYDHQAWXKIMO-ROUUACIJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H31N3O5
Molecular Weight 465.50 g/mol
Exact Mass 465.22637110 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.08
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Amoenamide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9417 94.17%
Caco-2 - 0.7729 77.29%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6731 67.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8349 83.49%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7930 79.30%
BSEP inhibitior + 0.9802 98.02%
P-glycoprotein inhibitior + 0.7878 78.78%
P-glycoprotein substrate + 0.7488 74.88%
CYP3A4 substrate + 0.6800 68.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8591 85.91%
CYP3A4 inhibition + 0.7211 72.11%
CYP2C9 inhibition - 0.5760 57.60%
CYP2C19 inhibition + 0.5275 52.75%
CYP2D6 inhibition - 0.7864 78.64%
CYP1A2 inhibition - 0.9176 91.76%
CYP2C8 inhibition + 0.5705 57.05%
CYP inhibitory promiscuity + 0.5411 54.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5641 56.41%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9658 96.58%
Skin irritation - 0.7940 79.40%
Skin corrosion - 0.9348 93.48%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6506 65.06%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.5265 52.65%
skin sensitisation - 0.8567 85.67%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity + 0.7952 79.52%
Acute Oral Toxicity (c) III 0.6535 65.35%
Estrogen receptor binding + 0.7381 73.81%
Androgen receptor binding + 0.6746 67.46%
Thyroid receptor binding + 0.5892 58.92%
Glucocorticoid receptor binding + 0.7413 74.13%
Aromatase binding + 0.5692 56.92%
PPAR gamma + 0.7725 77.25%
Honey bee toxicity - 0.8437 84.37%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9734 97.34%

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
CHEMBL2581 P07339 Cathepsin D 98.15% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.94% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.36% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.97% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.76% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.34% 97.25%
CHEMBL1902 P62942 FK506-binding protein 1A 95.71% 97.05%
CHEMBL3524 P56524 Histone deacetylase 4 92.26% 92.97%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.13% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.52% 95.56%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 90.79% 91.03%
CHEMBL332 P03956 Matrix metalloproteinase-1 89.76% 94.50%
CHEMBL4208 P20618 Proteasome component C5 89.67% 90.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 87.39% 90.08%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.06% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.78% 89.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 85.65% 82.38%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.37% 99.23%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 85.24% 90.93%
CHEMBL3310 Q96DB2 Histone deacetylase 11 84.62% 88.56%
CHEMBL340 P08684 Cytochrome P450 3A4 84.51% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.29% 97.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.14% 93.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.09% 90.24%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.93% 93.04%
CHEMBL2803 P43403 Tyrosine-protein kinase ZAP-70 81.93% 82.50%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.38% 95.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.54% 90.71%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.23% 97.50%

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 132580454
LOTUS LTS0115089
wikiData Q104968035