Chrysogenamide A

Details

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Internal ID d20b80ac-7547-4a5b-817f-d897937bb036
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acid amides
IUPAC Name (1'S,3S,4'S,8'S)-4',11',11'-trimethyl-7-(3-methylbut-2-enyl)spiro[1H-indole-3,12'-3,14-diazatetracyclo[6.5.2.01,10.03,8]pentadecane]-2,15'-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H37N3O2/c1-17(2)11-12-19-9-6-10-20-22(19)29-24(33)28(20)15-26-16-31-18(3)8-7-13-27(31,23(32)30-26)14-21(26)25(28,4)5/h6,9-11,18,21H,7-8,12-16H2,1-5H3,(H,29,33)(H,30,32)/t18-,21?,26+,27-,28-/m0/s1
InChI Key OFVLVORZFFTHHV-OJLVKCQKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H37N3O2
Molecular Weight 447.60 g/mol
Exact Mass 447.28857743 g/mol
Topological Polar Surface Area (TPSA) 61.40 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.32
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Chrysogenamide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 - 0.6686 66.86%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6067 60.67%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.8877 88.77%
OATP1B3 inhibitior + 0.9377 93.77%
MATE1 inhibitior - 0.8209 82.09%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9707 97.07%
P-glycoprotein inhibitior + 0.6997 69.97%
P-glycoprotein substrate + 0.6917 69.17%
CYP3A4 substrate + 0.6650 66.50%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate + 0.4046 40.46%
CYP3A4 inhibition + 0.5071 50.71%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.5198 51.98%
CYP2D6 inhibition - 0.7215 72.15%
CYP1A2 inhibition - 0.7415 74.15%
CYP2C8 inhibition - 0.5662 56.62%
CYP inhibitory promiscuity + 0.6267 62.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6232 62.32%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9810 98.10%
Skin irritation - 0.7798 77.98%
Skin corrosion - 0.9028 90.28%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9000 90.00%
Micronuclear + 0.6600 66.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8457 84.57%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.8082 80.82%
Acute Oral Toxicity (c) III 0.6022 60.22%
Estrogen receptor binding + 0.6909 69.09%
Androgen receptor binding + 0.7620 76.20%
Thyroid receptor binding + 0.6782 67.82%
Glucocorticoid receptor binding + 0.6450 64.50%
Aromatase binding + 0.7406 74.06%
PPAR gamma + 0.6915 69.15%
Honey bee toxicity - 0.8254 82.54%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9816 98.16%

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 97.99% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.97% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.51% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.22% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.17% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.46% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.29% 85.14%
CHEMBL1937 Q92769 Histone deacetylase 2 92.51% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.09% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.48% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.47% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.55% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.34% 82.69%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.72% 93.99%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.23% 93.03%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.09% 91.24%
CHEMBL1902 P62942 FK506-binding protein 1A 82.79% 97.05%
CHEMBL221 P23219 Cyclooxygenase-1 82.43% 90.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.87% 99.23%
CHEMBL3524 P56524 Histone deacetylase 4 80.01% 92.97%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139584637
LOTUS LTS0117186
wikiData Q77372942