T6514
Oleandomycin triacetate
Synonym(s):
Troleandomycin
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About This Item
Empirical Formula (Hill Notation):
C41H67NO15
CAS Number:
Molecular Weight:
813.97
UNSPSC Code:
51101500
EC Number:
220-392-9
Beilstein/REAXYS Number:
1418238
MDL number:
SMILES string
CO[C@H]1C[C@@H](O[C@@H](C)[C@@H]1OC(C)=O)O[C@H]2[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3OC(C)=O)N(C)C)[C@@H](C)C[C@@]4(CO4)C(=O)[C@H](C)[C@@H](OC(C)=O)[C@@H](C)[C@@H](C)OC(=O)[C@@H]2C
mode of action
enzyme | inhibits, protein synthesis | interferes
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General description
Chemical structure: macrolide
wgk
WGK 2
Storage Class
13 - Non Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
涉药品监管产品
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Daniel R Albaugh et al.
Drug metabolism and disposition: the biological fate of chemicals, 40(7), 1336-1344 (2012-04-12)
The current studies assessed the utility of freshly plated hepatocytes, cryopreserved plated hepatocytes, and cryopreserved plated HepaRG cells for the estimation of inactivation parameters k(inact) and K(I) for CYP3A. This was achieved using a subset of CYP3A time-dependent inhibitors (fluoxetine
Soo H Bae et al.
The Journal of pharmacy and pharmacology, 61(12), 1637-1642 (2009-12-05)
It has been reported that hepatic cytochrome P450 (CYP)2C9 and CYP3A4 are responsible for the metabolism of sildenafil and formation of its metabolite, N-desmethylsildenafil, in humans. However, in-vivo studies in rats have not been reported. Sildenafil (20 mg/kg) was administered
Güliz Gürel et al.
Antimicrobial agents and chemotherapy, 53(12), 5010-5014 (2009-09-10)
Structures have been obtained for the complexes that triacetyloleandomycin and mycalamide A form with the large ribosomal subunit of Haloarcula marismortui. Triacetyloleandomycin binds in the nascent peptide tunnel and inhibits the activity of ribosomes by blocking the growth of the
Shobana Ganesan et al.
Toxicology and applied pharmacology, 241(1), 14-22 (2009-07-21)
Primaquine, an 8-aminoquinoline, is the drug of choice for radical cure of relapsing malaria. Use of primaquine is limited due to its hemotoxicity, particularly in populations with glucose-6-phosphate dehydrogenase deficiency [G6PD(-)]. Biotransformation appears to be central to the anti-infective and
E Y Oh et al.
British journal of pharmacology, 151(1), 24-34 (2007-03-14)
Recently, orthostatic hypotension was observed in patients with benign prostatic hyperplasia who are taking vardenafil (a PDE 5 inhibitor) and terazosin (a long acting alpha blocker). Therefore, this study was performed with DA-8159 (a long acting PDE 5 inhibitor) and
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