TMC-69

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Category Mycotoxins
Catalog number BBF-02529
CAS
Molecular Weight 421.5
Molecular Formula C26H31NO4

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Description

TMC-69 is an antitumor antibiotic isolated from the fermentation broth of a fungal strain Chrysosporium sp. TC 1068. It exhibited moderate in vitro cytotoxic activity.

Specification

Synonyms TMC 69
IUPAC Name 1,4-dihydroxy-3-[(2R,3R,5Z)-3-methyl-5-[(2E,4E)-6-methylocta-2,4-dienylidene]oxan-2-yl]-5-phenylpyridin-2-one
Canonical SMILES CCC(C)C=CC=CC=C1CC(C(OC1)C2=C(C(=CN(C2=O)O)C3=CC=CC=C3)O)C
InChI InChI=1S/C26H31NO4/c1-4-18(2)11-7-5-8-12-20-15-19(3)25(31-17-20)23-24(28)22(16-27(30)26(23)29)21-13-9-6-10-14-21/h5-14,16,18-19,25,28,30H,4,15,17H2,1-3H3/b8-5+,11-7+,20-12-/t18?,19-,25-/m1/s1
InChI Key IXMWFEZJSGIEGP-OGFVGMJFSA-N

Properties

Antibiotic Activity Spectrum neoplastics (Tumor)

Reference Reading

1. TMC-69, a new antitumor antibiotic with Cdc25A inhibitory activity, produced by Chrysosporium sp. TC1068. Taxonomy, fermentation and biological activities
N Hirano, J Kohno, S Tsunoda, M Nishio, N Kishi, T Okuda, K Kawano, S Komatsubara, N Nakanishi J Antibiot (Tokyo). 2001 May;54(5):421-7. doi: 10.7164/antibiotics.54.421.
A new antibiotic designated TMC-69 has been isolated from the fermentation broth of a fungal strain Chrysosporium sp. TC 1068. TMC-69 exhibited moderate in vitro cytotoxic activity. TMC-69-6H, a derivative of TMC-69 prepared by hydrogenation, possessed more potent in vitro cytotoxicity than TMC-69, and exhibited in vivo antitumor activity against murine P388 leukemia and B16 melanoma. TMC-69-6H was found to specifically inhibit Cdc25A and B phosphatases.

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Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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