SCS-C007284

aspergillamide A

Pathway: Amino acids and Peptides Superclass: Small peptides Class: Dipeptides

Chemical Structure

Structure of aspergillamide A
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3D conformers are computationally generated from SMILES by RDKit for visualization and download; they are not experimental crystal or NMR structures.
Download: SDF SMILES

Source Information

Aspergillus terreus (mangrove endophytic fungus)
Kingdom Fungi Phylum Ascomycota Class Eurotiomycetes Order Eurotiales Family Aspergillaceae Genus Aspergillus Species Aspergillus terreus
South China Sea
DOI: 10.1016/s1875-5364(19)30017-2  · Chinese Journal of Natural Medicines

Drug-likeness (Lipinski Ro5)

Molecular Weight
474.6 Da
Threshold ≤ 500
ALogP
3.88
Threshold ≤ 5
H-Bond Donors
3
Threshold ≤ 5
H-Bond Acceptors
3
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C28H34N4O3
Molecular Weight:
474.6050 Da
SMILES:
CC(=O)N[C@@H](CC(C)C)C(=O)N(C)[C@@H](Cc1ccccc1)C(=O)N/C=C\c1c[nH]c2ccccc12
InChIKey:
UTJKZLHQWWNPPP-JTVZBIPBSA-N
InChI:
InChI=1S/C28H34N4O3/c1-19(2)16-25(31-20(3)33)28(35)32(4)26(17-21-10-6-5-7-11-21)27(34)29-15-14-22-18-30-24-13-9-8-12-23(22)24/h5-15,18-19,25-26,30H,16-17H2,1-4H3,(H,29,34)(H,31,33)/b15-14-/t25-,26-/m0/s1
Calculated Properties
ALogP:
3.875 lipophilicity
TPSA:
94.30 Ų polar surface area
H-Bond Donors:
3
H-Bond Acceptors:
3
Rotatable Bonds:
10
Ring Count:
3 (3 aromatic)
Chiral Centers:
2
Fsp³:
0.3214 fraction sp³ carbon

Database Information

Compound ID:
SCS-C007284
NPClassifier Pathway:
Amino acids and Peptides
NPClassifier Superclass:
Small peptides
NPClassifier Class:
Dipeptides
Glycoside:
No
NPClassifier Status:
Classified
External Links:

Biological Activity Data

Activity values are displayed only when a quantitative or clearly reported result is available. Tested organisms, cell lines and molecular targets are shown under Target / model.
Activity Assay Target / model Result Reference
Antimycobacterial inhibition rate Mycobacterium tuberculosis protein tyrosine phosphatase B (MptpB) < 60.0 % 10.1016/s1875-5364(19)30017-2 Chinese Journal of Natural Medicines
Antitumor activity level human glioma U87 cells all these compounds (1?17) exhibited weak or no cytotoxic activities towards human glioma U87 cells at a concentration of 10 μmol·L?1 10.1016/s1875-5364(19)30017-2 Chinese Journal of Natural Medicines
Neuroprotective / Neuromodulatory activity level glutamate-induced toxicity in HT22 cells — Structured numeric value is not available in this record; see the primary reference. 10.1016/s1875-5364(19)30017-2 Chinese Journal of Natural Medicines
Structure enlarged