14-O-Acetylindolactam V
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
| Category | Antibiotics |
| Catalog number | BBF-00006 |
| CAS | 91403-61-1 |
| Molecular Weight | 343.42 |
| Molecular Formula | C19H25N3O3 |
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Description
14-O-Acetylindolactam V is an antibiotic isolated from the Actinomyces NA34-17. 14-O-Acetylindolactam V has the effect of inducing early Epstein-Barr virus antigen.
Specification
| Synonyms | 2S)-1-Methyl-5alpha-(acetoxymethyl)-2beta-isopropyl-1,2,4,5,6,8-hexahydro-3H-pyrrolo[4,3,2-gh]-1,4-benzodiazonine-3-one; [(2S,5S)-1-methyl-3-oxo-2-(propan-2-yl)-2,3,4,5,6,8-hexahydro-1H-[1,4]diazonino[7,6,5-cd]indol-5-yl]methyl acetate |
| IUPAC Name | [(10S,13S)-9-methyl-11-oxo-10-propan-2-yl-3,9,12-triazatricyclo[6.6.1.04,15]pentadeca-1,4(15),5,7-tetraen-13-yl]methyl acetate |
| Canonical SMILES | CC(C)C1C(=O)NC(CC2=CNC3=C2C(=CC=C3)N1C)COC(=O)C |
| InChI | InChI=1S/C19H25N3O3/c1-11(2)18-19(24)21-14(10-25-12(3)23)8-13-9-20-15-6-5-7-16(17(13)15)22(18)4/h5-7,9,11,14,18,20H,8,10H2,1-4H3,(H,21,24)/t14-,18-/m0/s1 |
| InChI Key | WJBVMJYASZWGBL-KSSFIOAISA-N |
Properties
| Appearance | Colorless Powder |
| Antibiotic Activity Spectrum | viruses |
| Boiling Point | 573.9°C at 760 mmHg |
| Melting Point | 100-110°C |
| Density | 1.154 g/cm3 |
Reference Reading
1. Structural basis of V-ATPase VO region assembly by Vma12p, 21p, and 22p
Hanlin Wang, Stephanie A Bueler, John L Rubinstein Proc Natl Acad Sci U S A. 2023 Feb 7;120(6):e2217181120. doi: 10.1073/pnas.2217181120. Epub 2023 Feb 1.
Vacuolar-type adenosine triphosphatases (V-ATPases) are rotary proton pumps that acidify specific intracellular compartments in almost all eukaryotic cells. These multi-subunit enzymes consist of a soluble catalytic V1 region and a membrane-embedded proton-translocating VO region. VO is assembled in the endoplasmic reticulum (ER) membrane, and V1 is assembled in the cytosol. However, V1 binds VO only after VO is transported to the Golgi membrane, thereby preventing acidification of the ER. We isolated VO complexes and subcomplexes from Saccharomyces cerevisiae bound to V-ATPase assembly factors Vma12p, Vma21p, and Vma22p. Electron cryomicroscopy shows how the Vma12-22p complex recruits subunits a, e, and f to the rotor ring of VO while blocking premature binding of V1. Vma21p, which contains an ER-retrieval motif, binds the VO:Vma12-22p complex, "mature" VO, and a complex that appears to contain a ring of loosely packed rotor subunits and the proteins YAR027W and YAR028W. The structures suggest that Vma21p binds assembly intermediates that contain a rotor ring and that activation of proton pumping following assembly of V1 with VO removes Vma21p, allowing V-ATPase to remain in the Golgi. Together, these structures show how Vma12-22p and Vma21p function in V-ATPase assembly and quality control, ensuring the enzyme acidifies only its intended cellular targets.
2. Vanadate Retention by Iron and Manganese Oxides
Macon J Abernathy, Michael V Schaefer, Roxana Ramirez, Abdi Garniwan, Ilkeun Lee, Francisco Zaera, Matthew L Polizzotto, Samantha C Ying ACS Earth Space Chem. 2022 Aug 18;6(8):2041-2052. doi: 10.1021/acsearthspacechem.2c00116. Epub 2022 Aug 5.
Anthropogenic emissions of vanadium (V) into terrestrial and aquatic surface systems now match those of geogenic processes, and yet, the geochemistry of vanadium is poorly described in comparison to other comparable contaminants like arsenic. In oxic systems, V is present as an oxyanion with a +5 formal charge on the V center, typically described as H x VO4 (3-x)-, but also here as V(V). Iron (Fe) and manganese (Mn) (oxy)hydroxides represent key mineral phases in the cycling of V(V) at the solid-solution interface, and yet, fundamental descriptions of these surface-processes are not available. Here, we utilize extended X-ray absorption fine structure (EXAFS) and thermodynamic calculations to compare the surface complexation of V(V) by the common Fe and Mn mineral phases ferrihydrite, hematite, goethite, birnessite, and pyrolusite at pH 7. Inner-sphere V(V) complexes were detected on all phases, with mononuclear V(V) species dominating the adsorbed species distribution. Our results demonstrate that V(V) adsorption is exergonic for a variety of surfaces with differing amounts of terminal -OH groups and metal-O bond saturations, implicating the conjunctive role of varied mineral surfaces in controlling the mobility and fate of V(V) in terrestrial and aquatic systems.
3. Coordinated conformational changes in the V1 complex during V-ATPase reversible dissociation
Thamiya Vasanthakumar, Kristine A Keon, Stephanie A Bueler, Michael C Jaskolka, John L Rubinstein Nat Struct Mol Biol. 2022 May;29(5):430-439. doi: 10.1038/s41594-022-00757-z. Epub 2022 Apr 25.
Vacuolar-type ATPases (V-ATPases) are rotary enzymes that acidify intracellular compartments in eukaryotic cells. These multi-subunit complexes consist of a cytoplasmic V1 region that hydrolyzes ATP and a membrane-embedded VO region that transports protons. V-ATPase activity is regulated by reversible dissociation of the two regions, with the isolated V1 and VO complexes becoming autoinhibited on disassembly and subunit C subsequently detaching from V1. In yeast, assembly of the V1 and VO regions is mediated by the regulator of the ATPase of vacuoles and endosomes (RAVE) complex through an unknown mechanism. We used cryogenic-electron microscopy of yeast V-ATPase to determine structures of the intact enzyme, the dissociated but complete V1 complex and the V1 complex lacking subunit C. On separation, V1 undergoes a dramatic conformational rearrangement, with its rotational state becoming incompatible for reassembly with VO. Loss of subunit C allows V1 to match the rotational state of VO, suggesting how RAVE could reassemble V1 and VO by recruiting subunit C.
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
