SCS-C001277

emodacidamide D

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

Chemical Structure

Structure of emodacidamide D
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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°0.544′ N
DOI: 10.1021/acs.jnatprod.7b00269  · Journal of Natural Products

Drug-likeness (Lipinski Ro5)

Molecular Weight
427.4 Da
Threshold ≤ 500
ALogP
1.90
Threshold ≤ 5
H-Bond Donors
4
Threshold ≤ 5
H-Bond Acceptors
8
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C22H21NO8
Molecular Weight:
427.4000 Da
SMILES:
CC[C@H](C)[C@H](NC(=O)c1cc(O)c2c(c1)C(=O)c1cc(O)cc(O)c1C2=O)C(=O)OC
InChIKey:
RHIKPDQWISFYIG-YYSFKGJASA-N
InChI:
InChI=1S/C22H21NO8/c1-4-9(2)18(22(30)31-3)23-21(29)10-5-12-16(14(25)6-10)20(28)17-13(19(12)27)7-11(24)8-15(17)26/h5-9,18,24-26H,4H2,1-3H3,(H,23,29)/t9-,18-/m0/s1
Calculated Properties
ALogP:
1.896 lipophilicity
TPSA:
150.23 Ų polar surface area
H-Bond Donors:
4
H-Bond Acceptors:
8
Rotatable Bonds:
5
Ring Count:
3 (2 aromatic)
Chiral Centers:
2
Fsp³:
0.2727 fraction sp³ carbon

Database Information

Compound ID:
SCS-C001277
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 IC50 Jurkat cells 12.0 μM 10.1021/acs.jnatprod.7b00269 Journal of Natural Products
Structure enlarged