Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Edit custom filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 2
2005 2
2006 1
2007 1
2016 1
2026 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

7 results

Results by year

Filters applied: . Clear all
Page 1
Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. I. Taxonomy, production, isolation and biological properties.
Igarashi M, Hayashi C, Homma Y, Hattori S, Kinoshita N, Hamada M, Takeuchi T. Igarashi M, et al. J Antibiot (Tokyo). 2000 Oct;53(10):1096-101. doi: 10.7164/antibiotics.53.1096. J Antibiot (Tokyo). 2000. PMID: 11132953 Free article.
A novel 16-membered lactone antibiotic named tubelactomicin A was isolated from the culture broth of an actinomycete strain. The producing organism, designated MK703-102F1, was identified as a member of Nocardia. ...Tubelactomicin A showed strong activity against ac …
A novel 16-membered lactone antibiotic named tubelactomicin A was isolated from the culture broth of an actinomycete strain. The prod …
Total synthesis of (+)-tubelactomicin A. 2. Synthesis of the upper-half segment and completion of the total synthesis.
Motozaki T, Sawamura K, Suzuki A, Yoshida K, Ueki T, Ohara A, Munakata R, Takao K, Tadano K. Motozaki T, et al. Org Lett. 2005 May 26;7(11):2265-7. doi: 10.1021/ol050763x. Org Lett. 2005. PMID: 15901185
We have completed the total synthesis of natural (+)-tubelactomicin A (1), a 16-membered macrolide antibiotic. This Letter presents a highly efficient synthesis of the upper-half segment (C14-C24) and the completion of the total synthesis featuring a high-yielding Stille c …
We have completed the total synthesis of natural (+)-tubelactomicin A (1), a 16-membered macrolide antibiotic. This Letter presents a …
Total synthesis of (+)-tubelactomicin A. 1. Stereoselective synthesis of the lower-half segment by an intramolecular Diels-Alder approach.
Motozaki T, Sawamura K, Suzuki A, Yoshida K, Ueki T, Ohara A, Munakata R, Takao K, Tadano K. Motozaki T, et al. Org Lett. 2005 May 26;7(11):2261-4. doi: 10.1021/ol0507625. Org Lett. 2005. PMID: 15901184
Starting from diethyl (R)-malate, synthesis of the lower-half segment of (+)-tubelactomicin A, a 16-membered macrolide antibiotic, has been achieved. The synthesis involved the highly endo- and pi-facial selective intramolecular Diels-Alder reaction achieved using a trisub …
Starting from diethyl (R)-malate, synthesis of the lower-half segment of (+)-tubelactomicin A, a 16-membered macrolide antibiotic, ha …
Hydroxyl-Assisted Carbonylation of Alkenyltin Derivatives: Development and Application to a Formal Synthesis of Tubelactomicin A.
Sommer H, Fürstner A. Sommer H, et al. Org Lett. 2016 Jul 1;18(13):3210-3. doi: 10.1021/acs.orglett.6b01431. Epub 2016 Jun 9. Org Lett. 2016. PMID: 27280547
Under the optimized conditions, competing proto-destannation is marginal; the method proved compatible with various (acid sensitive) functional groups and was applied to a short formal total synthesis of the antibiotic tubelactomicin A....
Under the optimized conditions, competing proto-destannation is marginal; the method proved compatible with various (acid sensitive) functio …
Tubelactomicin A, a novel 16-membered lactone antibiotic, from Nocardia sp. II. Structure elucidation.
Igarashi M, Nakamura H, Naganawa H, Takeuchi T. Igarashi M, et al. J Antibiot (Tokyo). 2000 Oct;53(10):1102-7. doi: 10.7164/antibiotics.53.1102. J Antibiot (Tokyo). 2000. PMID: 11132954 Free article.
A novel 16-membered lactone antibiotic named tubelactomicin A was isolated from the culture broth of Nocaradia sp. MK703-102F1. The structure of tubelactomicin A was assigned by spectroscopic analysis and the absolute configuration was determined by X-ray crystallog …
A novel 16-membered lactone antibiotic named tubelactomicin A was isolated from the culture broth of Nocaradia sp. MK703-102F1. The s …
Total syntheses of polyketide-derived bioactive natural products.
Tatsuta K, Hosokawa S. Tatsuta K, et al. Chem Rec. 2006;6(4):217-33. doi: 10.1002/tcr.20084. Chem Rec. 2006. PMID: 16900486 Review.
The target bioactive polyketides are classified into three categories according to their structures: (i) lactone-fused polycyclic compounds [(+)-cochleamycin A, (+)-tubelactomicin A, and (-)-tetrodecamycin], (ii) aromatic compounds [(-)-tetracycline, (-)-BE-54238B, lymphos …
The target bioactive polyketides are classified into three categories according to their structures: (i) lactone-fused polycyclic compounds …
Total syntheses of natural tubelactomicins B, D, and E: establishment of their stereochemistries.
Sawamura K, Yoshida K, Suzuki A, Motozaki T, Kozawa I, Hayamizu T, Munakata R, Takao K, Tadano K. Sawamura K, et al. J Org Chem. 2007 Aug 3;72(16):6143-8. doi: 10.1021/jo0708442. Epub 2007 Jul 11. J Org Chem. 2007. PMID: 17625888
Total syntheses of the antimicrobial tricyclic 16-membered macrolides, (+)-tubelactomicin B, (+)-tubelactomicin D, and (+)-tubelactomicin E, have been accomplished for the first time with common synthetic approaches. These total syntheses established the rela …
Total syntheses of the antimicrobial tricyclic 16-membered macrolides, (+)-tubelactomicin B, (+)-tubelactomicin D, and (+)- …