SCS-C004504

cordyheptapeptide E

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

Chemical Structure

Structure of cordyheptapeptide E
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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/np300152d  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
896.1 Da
Threshold ≤ 500
ALogP
2.79
Threshold ≤ 5
H-Bond Donors
5
Threshold ≤ 5
H-Bond Acceptors
9
Threshold ≤ 10
1 violation (MW) — borderline drug-like

Chemical Properties

Molecular Formula:
C49H65N7O9
Molecular Weight:
896.0990 Da
SMILES:
CC[C@@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)N(C)C(=O)[C@H](Cc2ccccc2)NC(=O)CN(C)C(=O)[C@@H]2CCCN2C(=O)[C@@H](Cc2ccc(O)cc2)N(C)C(=O)[C@H](CC(C)C)NC1=O
InChIKey:
RSKSPMHQQIYPNU-CWAWLLILSA-N
InChI:
InChI=1S/C49H65N7O9/c1-8-31(4)43-45(61)51-37(25-30(2)3)46(62)55(7)41(28-34-18-22-36(58)23-19-34)49(65)56-24-12-15-39(56)48(64)53(5)29-42(59)50-38(26-32-13-10-9-11-14-32)47(63)54(6)40(44(60)52-43)27-33-16-20-35(57)21-17-33/h9-11,13-14,16-23,30-31,37-41,43,57-58H,8,12,15,24-29H2,1-7H3,(H,50,59)(H,51,61)(H,52,60)/t31-,37+,38+,39+,40+,41-,43+/m1/s1
Calculated Properties
ALogP:
2.789 lipophilicity
TPSA:
209.00 Ų polar surface area
H-Bond Donors:
5
H-Bond Acceptors:
9
Rotatable Bonds:
10
Ring Count:
5 (3 aromatic)
Chiral Centers:
7
Fsp³:
0.4898 fraction sp³ carbon

Database Information

Compound ID:
SCS-C004504
NPClassifier Pathway:
Amino acids and Peptides
NPClassifier Superclass:
Oligopeptides
NPClassifier Class:
Cyclic peptides
Glycoside:
No
NPClassifier Status:
Classified
External Links:

Biological Activity Data

No bioactivity data available for this compound.

Structure enlarged