Compound ID | 2635

Mycobacidin

Synonym(s): Actithiazic acid  |  acidomycin  |  cinnamonin  |  thiazolidone antibiotic PA-95

Class: Natural product antibiotic

Details of activity: Active against mycobacteria (inactive against nontuberculous mycobacteria); biotin synthesis inhibitor
Description: Natural product from Streptomyces virginiae, S. myceticus, S. roseochromogenes, and S. lavendulae; pharmacologically inert/ rapidly eliminated by host; contains a thiazolidine core
Year first mentioned: 1952
Development status: Inactive
Chemical structure(s):
Click here for structure editor
Molecular weight: 217.29
Iso. SMILES: C1C(=O)NC(S1)CCCCCC(=O)O
InChI Key: CSOJYIADHHNGRM-UHFFFAOYSA-N
Can. SMILES: C(CCC1NC(=O)CS1)CCC(=O)O
InChI: InChI=1S/C9H15NO3S/c11-7-6-14-8(10-7)4-2-1-3-5-9(12)13/h8H,1-6H2,(H,10,11)(H,12,13)
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/94170
Citations:
  • https://pdf.sciencedirectassets.com/271363/1-s2.0-S0008621500X03771/1-s2.0-000862158780054X/main.pdf?X-Amz-Security-Token=IQoJb3JpZ2luX2VjEFMaCXVzLWVhc3QtMSJIMEYCIQCD46Gfe%2FhSTyJHsXOee%2Bt96VpYkmXuW932Rm1nUewoPAIhAOMwNl1ugEqtHqD6uhc8GvRzYUiaWNETl%2B2d7XrcHJJCKrwFCOz%2F%2F%2F%2F%2F%2F%2F%2F%2F%2FwEQBRoMMDU5MDAzNTQ2ODY1Igz46AMpjTKNFJQ79k0qkAXIKOk6icqeRP8kLdSTCiYOKx9X5WS9JDSHJX%2FsJs4q7m3PmNpLvm3rq2mAQ%2FUxpfk52kg8fBAmWOJKrMWCmtHWSCplCZCbIBCx8j6EV%2FbwC3JaWBLZuXH12VMjAqttrd1E56FWGlADBuTxv6rcY9p7rPhdNSCkF65SCvn%2FU76E%2BEySxRq1%2FNVXcMaVUAdpsjz7G%2F3UvTwyRL4W%2FQrb%2BNmPxP%2F%2B%2B4xkgh8R7HhYNFPPcmRI1QWXOynQtpt4AQFtLSxWWYRHXBeI0SXgjJi4QdKoGqH%2FYWt0BMFNYJIcFVeGgfHetBCLEcGwNW0BNsrLMpBacq%2BbkoyLHCwGB9AXP2iVamOouV5222Gvyn1GVSds4TJEu1RDhNxW7Ypgp5dAf5L0eOWFjI3KIRHkSh%2FUdesp%2FYpDFePAzgC9kYMTCY2p8PbQOQYrL4s7UPskPgZGBzJskfascRfn1D44qkJ5tJMfZY57f6Yw%2FKWbBbjSwRjZmoj29r92caRhqW%2B7w6cYc5NtPCye8L5MMZing73ueUSYzZlfijlxavvkUjFyuV6tRtrWNlr8cvQr5J2n7xreM75yeDB1cLXIwNs0wwaS%2Bkedrjh4G%2BxZTlhK59izzdPVZGppli18mIEkT1QcrHRoMu%2Bv1eAr7puZzXbe8H6iXwqNfSfO6bgjWeZPxjG8Bxu9lW92dT5jy2SJ3jbsLAqXacBT%2FOem5L1tGSNgQuRxTdQY9%2FEdcgzAsWwKj4JXG4TRvCHjPOlDI%2BGkIkEGxbrgseWe0D5QhXiZ1%2BEGRkYxdKqQn2xqGZKsTb6vZ4R52zUN5H3p5R4gI0c4AGxGy3R0RcZFpwpm8mRy1o%2BgfsiVA8sGu4U1afKuYlde%2BLLJy%2Fa9mzDkvvSsBjqwAYgkzve%2FueMQQU9oXDCcscTxbpM8ZnaaqUW1lzTGOr16%2FH0hvAJ8XmgCeIWDk2yL4UN3jUQ5pHlqFpN5gy7msrouBIg%2BWSwZ2%2F60hGzr6RzdSUNBS3e73uaDpoVIoTIQXUpJLeu%2BHEjUFmV%2BPGMNk%2B8SQypjwWtyqSY9HOGTUg5NRn%2Fy48a9WYW4BpyAWBs4x5xRagaj9eW7rtwB6iFwG0YfowRX%2FGvSWlv1kg1xsqF0&X-Amz-Algorithm=AWS4-HMAC-SHA256&X-Amz-Date=20240109T110812Z&X-Amz-SignedHeaders=host&X-Amz-Expires=300&X-Amz-Credential=ASIAQ3PHCVTY7AZA4BXB%2F20240109%2Fus-east-1%2Fs3%2Faws4_request&X-Amz-Signature=9a610e4b07dc27ac13621d93dbcca6267709a615d4b3d19298cd4af56bb7b159&hash=885e02d50c1c6613eee46ca67ebb82e35e22bd82066d306693ca9308656b1aaf&host=68042c943591013ac2b2430a89b270f6af2c76d8dfd086a07176afe7c76c2c61&pii=000862158780054X&tid=spdf-b0545169-e7b6-4c46-8cb8-59c081953ebc&sid=8d6ddce17e808045f76b8153e38fcf44565dgxrqb&type=client&tsoh=d3d3LnNjaWVuY2VkaXJlY3QuY29t&ua=1d045b5b510c53595c5054&rr=842c38903f7b075b&cc=gb
  • https://pubs.acs.org/doi/10.1021/acsinfecdis.8b00345
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