SCS-C001280

emodacidamide G

Pathway: Polyketides Superclass: Polycyclic aromatic polyketides Class: Anthraquinones and anthrones

Chemical Structure

Structure of emodacidamide G
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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

Penicillium sp. SCSIO sof101 (soft coral-derived fungus)
South China Sea  · -2448m  · 112°124′ E, 18°0.547′ N
DOI: 10.1021/acs.jnatprod.7b00269  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
447.8 Da
Threshold ≤ 500
ALogP
2.46
Threshold ≤ 5
H-Bond Donors
5
Threshold ≤ 5
H-Bond Acceptors
7
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C21H18ClNO8
Molecular Weight:
447.8000 Da
SMILES:
CC(C)C[C@H](NC(=O)c1cc(O)c2c(c1)C(=O)c1cc(O)c(Cl)c(O)c1C2=O)C(=O)O
InChIKey:
VOXKCJAIEWKHLK-NSHDSACASA-N
InChI:
InChI=1S/C21H18ClNO8/c1-7(2)3-11(21(30)31)23-20(29)8-4-9-14(12(24)5-8)18(27)15-10(17(9)26)6-13(25)16(22)19(15)28/h4-7,11,24-25,28H,3H2,1-2H3,(H,23,29)(H,30,31)/t11-/m0/s1
Calculated Properties
ALogP:
2.461 lipophilicity
TPSA:
161.23 Ų polar surface area
H-Bond Donors:
5
H-Bond Acceptors:
7
Rotatable Bonds:
5
Ring Count:
3 (2 aromatic)
Chiral Centers:
1
Fsp³:
0.2381 fraction sp³ carbon

Database Information

Compound ID:
SCS-C001280
NPClassifier Pathway:
Polyketides
NPClassifier Superclass:
Polycyclic aromatic polyketides
NPClassifier Class:
Anthraquinones and anthrones
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
Antitumor — Jurkat cells 20.0 μM 10.1021/acs.jnatprod.7b00269 Journal of Natural Products
Structure enlarged