Compound ID | 2566

Update compound information

Hapalindole T

Class: Natural product antibiotic

Agent Type: Natural product; Small molecule;
Spectrum of activity: Gram-positive
Mechanism of action: Unknown
Target Pathogen: Active against Staphylococcus aureus
Description: Natural product from cyanobacteria (Fischerella sp.)
Year first mentioned: 2009
Development status: Experimental
Chemical structure(s):
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Molecular weight: 386.94
Iso. SMILES: C[C@@]1([C@@H](C[C@H]2[C@@]3([C@H]1NC(=O)S3)C4=CNC5=CC=CC(=C54)C2(C)C)Cl)C=C
InChI Key: HQHRKXNDJILQCX-NFWXSOHESA-N
Can. SMILES: C=C[C@@]1(C)[C@@H](C[C@@H]2C(C)(C)C3=CC=CC4=C3C(=CN4)[C@]25[C@H]1NC(=O)S5)Cl
InChI: InChI=1S/C21H23ClN2OS/c1-5-20(4)15(22)9-14-19(2,3)11-7-6-8-13-16(11)12(10-23-13)21(14)17(20)24-18(25)26-21/h5-8,10,14-15,17,23H,1,9H2,2-4H3,(H,24,25)/t14-,15-,17+,20+,21-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/21671523
Citation: https://pubs.acs.org/doi/10.1021/acscatal.0c05656

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