SCS-C006971

acrechalasin F

Pathway: Alkaloids Superclass: Pseudoalkaloids Class: Cytochalasan alkaloids

Chemical Structure

Structure of acrechalasin F
Loading 3D structure...
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 implicatum (NA)
Original source name: Acremonium implicatum | A. implicatum
Nansha Islands  · 9°39′29.75" N, 112°59′09.84" E
DOI: 10.1016/j.phytochem.2025.114655  · Phytochemistry

Drug-likeness (Lipinski Ro5)

Molecular Weight
449.6 Da
Threshold ≤ 500
ALogP
3.97
Threshold ≤ 5
H-Bond Donors
3
Threshold ≤ 5
H-Bond Acceptors
4
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C28H35NO4
Molecular Weight:
449.5910 Da
SMILES:
C=C1[C@@H](C)[C@H]2[C@H](Cc3ccccc3O)NC(=O)[C@]23C(=O)/C=C/[C@@H](C)C[C@@H](C)C/C=C/[C@H]3[C@@H]1O
InChIKey:
KPSCZCHMHWHGHU-GMUALLFNSA-N
InChI:
InChI=1S/C28H35NO4/c1-16-8-7-10-21-26(32)19(4)18(3)25-22(15-20-9-5-6-11-23(20)30)29-27(33)28(21,25)24(31)13-12-17(2)14-16/h5-7,9-13,16-18,21-22,25-26,30,32H,4,8,14-15H2,1-3H3,(H,29,33)/b10-7+,13-12+/t16-,17+,18+,21-,22-,25-,26+,28+/m0/s1
Calculated Properties
ALogP:
3.966 lipophilicity
TPSA:
86.63 Ų polar surface area
H-Bond Donors:
3
H-Bond Acceptors:
4
Rotatable Bonds:
2
Ring Count:
4 (1 aromatic)
Chiral Centers:
8
Fsp³:
0.5000 fraction sp³ carbon

Database Information

Compound ID:
SCS-C006971
NPClassifier Pathway:
Alkaloids
NPClassifier Superclass:
Pseudoalkaloids
NPClassifier Class:
Cytochalasan alkaloids
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
Anti-inflammatory IC50 nitric oxide production — Structured numeric value is not available in this record; see the primary reference. 10.1016/j.phytochem.2025.114655 Phytochemistry
Structure enlarged