Aspergilumamide A

Details

Top
Internal ID 17f52417-34c0-4ff0-a60f-49d4edd83392
Taxonomy Organoheterocyclic compounds > Pteridines and derivatives
IUPAC Name methyl 2-[[(2S)-5-amino-2-[(1,3-dimethyl-2,4-dioxopteridine-6-carbonyl)amino]-5-oxopentanoyl]amino]benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H23N7O7/c1-28-17-16(20(33)29(2)22(28)35)25-14(10-24-17)19(32)27-13(8-9-15(23)30)18(31)26-12-7-5-4-6-11(12)21(34)36-3/h4-7,10,13H,8-9H2,1-3H3,(H2,23,30)(H,26,31)(H,27,32)/t13-/m0/s1
InChI Key MEICOTRNKNPKQV-ZDUSSCGKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C22H23N7O7
Molecular Weight 497.50 g/mol
Exact Mass 497.16589610 g/mol
Topological Polar Surface Area (TPSA) 194.00 Ų
XlogP -0.50
Atomic LogP (AlogP) -1.18
H-Bond Acceptor 11
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Aspergilumamide A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8437 84.37%
Caco-2 - 0.8771 87.71%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Nucleus 0.3943 39.43%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.8988 89.88%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8639 86.39%
BSEP inhibitior + 0.8286 82.86%
P-glycoprotein inhibitior + 0.7074 70.74%
P-glycoprotein substrate + 0.6544 65.44%
CYP3A4 substrate + 0.6835 68.35%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8723 87.23%
CYP3A4 inhibition - 0.7316 73.16%
CYP2C9 inhibition - 0.7535 75.35%
CYP2C19 inhibition - 0.7318 73.18%
CYP2D6 inhibition - 0.9404 94.04%
CYP1A2 inhibition - 0.6963 69.63%
CYP2C8 inhibition + 0.5420 54.20%
CYP inhibitory promiscuity - 0.7454 74.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6260 62.60%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9765 97.65%
Skin irritation - 0.8078 80.78%
Skin corrosion - 0.9449 94.49%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4780 47.80%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.5034 50.34%
skin sensitisation - 0.9086 90.86%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.7659 76.59%
Acute Oral Toxicity (c) III 0.6406 64.06%
Estrogen receptor binding - 0.5385 53.85%
Androgen receptor binding + 0.6109 61.09%
Thyroid receptor binding + 0.5986 59.86%
Glucocorticoid receptor binding + 0.7137 71.37%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6947 69.47%
Honey bee toxicity - 0.8426 84.26%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.4432 44.32%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.35% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 96.88% 82.69%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.14% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 92.82% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.82% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.65% 99.23%
CHEMBL2581 P07339 Cathepsin D 92.59% 98.95%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 92.17% 94.42%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 90.92% 95.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.24% 94.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.54% 81.11%
CHEMBL2535 P11166 Glucose transporter 88.66% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.27% 95.56%
CHEMBL3714130 P46095 G-protein coupled receptor 6 88.18% 97.36%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.57% 95.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.37% 93.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.29% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.74% 96.67%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.54% 91.07%
CHEMBL2096618 P11274 Bcr/Abl fusion protein 84.42% 85.83%
CHEMBL3891 P07384 Calpain 1 83.52% 93.04%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.50% 96.00%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 81.11% 100.00%
CHEMBL2321614 Q9NPC2 Potassium channel subfamily K member 9 81.00% 80.00%

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 139584586
LOTUS LTS0251126
wikiData Q77371895