SCS-C008193

acremonpeptide C

Pathway: Amino acids and Peptides Superclass: Oligopeptides Class: Cyclic peptides

Chemical Structure

Structure of acremonpeptide C
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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

Acremonium persicinum (NA)
South China Sea
DOI: 10.1021/acs.jnatprod.9b00545  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
924.1 Da
Threshold ≤ 500
ALogP
0.49
Threshold ≤ 5
H-Bond Donors
9
Threshold ≤ 5
H-Bond Acceptors
12
Threshold ≤ 10
3 violations (MW, HBD, HBA) — not drug-like by Ro5

Chemical Properties

Molecular Formula:
C45H65N9O12
Molecular Weight:
924.0660 Da
SMILES:
CC(=O)N(O)CCC[C@@H]1NC(=O)[C@H](CCCN(O)C(C)=O)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](CCCN(O)C(C)=O)NC1=O
InChIKey:
XHQSGNPILRSDKT-BGBFCPIGSA-N
InChI:
InChI=1S/C45H65N9O12/c1-28(2)25-37-43(61)51-38(26-32-15-8-6-9-16-32)44(62)48-35(20-13-23-53(65)30(4)56)41(59)46-34(19-12-22-52(64)29(3)55)40(58)47-36(21-14-24-54(66)31(5)57)42(60)50-39(45(63)49-37)27-33-17-10-7-11-18-33/h6-11,15-18,28,34-39,64-66H,12-14,19-27H2,1-5H3,(H,46,59)(H,47,58)(H,48,62)(H,49,63)(H,50,60)(H,51,61)/t34-,35-,36-,37-,38-,39-/m0/s1
Calculated Properties
ALogP:
0.494 lipophilicity
TPSA:
296.22 Ų polar surface area
H-Bond Donors:
9
H-Bond Acceptors:
12
Rotatable Bonds:
18
Ring Count:
3 (2 aromatic)
Chiral Centers:
6
Fsp³:
0.5333 fraction sp³ carbon

Database Information

Compound ID:
SCS-C008193
NPClassifier Pathway:
Amino acids and Peptides
NPClassifier Superclass:
Oligopeptides
NPClassifier Class:
Cyclic peptides
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
Antimicrobial — Panel of tested bacteria and fungi 1?5 proved inactive in these assays at concentrations up to 100 μg/mL 10.1021/acs.jnatprod.9b00545 Journal of Natural Products
Structure enlarged