Molecule

Chloromyxamide A

AlkaPlorer ID: AK116160

Synonym: None

IUPAC Name: (2S)-1-[(2S)-1-[(2S)-2-[[(2S,5S,6S)-6-(chloromethyl)-5-methoxypiperidine-2-carbonyl]amino]-3-methylbutanoyl]piperidine-2-carbonyl]pyrrolidine-2-carboxylic acid

Structure

SMILES: CO[C@H]1CC[C@@H](C(O)=N[C@H](C(=O)N2CCCC[C@H]2C(=O)N2CCC[C@H]2C(=O)O)C(C)C)N[C@@H]1CCl

InChI: InChI=1S/C24H39ClN4O6/c1-14(2)20(27-21(30)15-9-10-19(35-3)16(13-25)26-15)23(32)28-11-5-4-7-17(28)22(31)29-12-6-8-18(29)24(33)34/h14-20,26H,4-13H2,1-3H3,(H,27,30)(H,33,34)/t15-,16+,17-,18-,19-,20-/m0/s1

InChIKey: RBXSKBXFOJTNHC-XSEPRYCASA-N

Reference

Structure, Total Synthesis, and Biosynthesis of Chloromyxamides: Myxobacterial Tetrapeptides Featuring an Uncommon 6‐Chloromethyl‐5‐methoxypipecolic Acid Building Block

PubChem CID: 146684617

LOTUS: LTS0119689

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NPAtlas: NPA028500

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Myxococcus sp.	Myxococcus	Myxococcaceae	Myxococcales	Myxococcia	Myxococcota	None	Bacteria

Properties Information

Molecule Weight: 515.0510000000003

TPSA？: 131.76999999999998

MolLogP？: 1.7986000000000024

Number of H-Donors: 3

Number of H-Acceptors: 6

RingCount: 3

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi