cyclo[DL-Leu-DL-OVal-DL-Val-DL-N(Me)Leu-Unk-DL-Val]

Base Information

• Chemical Name: cyclo[DL-Leu-DL-OVal-DL-Val-DL-N(Me)Leu-Unk-DL-Val]
• CAS No.: 2900-38-1
• Molecular Formula: C₃₃H₅₈N₄O₈
• Molecular Weight: 638.846
• NSC Number: 122224
• DSSTox Substance ID: DTXSID70951616
• Wikidata: Q105103317
• ChEMBL ID: CHEMBL2002215
• Mol file: 2900-38-1.mol

Synonyms:NSC122224;CHEMBL2002215;DTXSID70951616;NCI60_000519;8,14,17-Trihydroxy-4,19-dimethyl-3,12-bis(2-methylpropyl)-6,9,15-tri(propan-2-yl)-1,10-dioxa-4,7,13,16-tetraazacycloicosa-7,13,16-triene-2,5,11-trione

Chemical Property of cyclo[DL-Leu-DL-OVal-DL-Val-DL-N(Me)Leu-Unk-DL-Val]

Chemical Property:

• Vapor Pressure: 1.13E-32mmHg at 25°C
• Melting Point: 261-263°
• Boiling Point: 894.4°Cat760mmHg
• Flash Point: 494.7°C
• PSA: 160.21000
• Density: 1.008g/cm³
• LogP: 3.74550
• XLogP3: 5.6
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 7
• Exact Mass: 638.42546482
• Heavy Atom Count: 45
• Complexity: 1040

Purity/Quality:

99% ^*data from raw suppliers

Sporidesmolide I ≥95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1CC(=O)NC(C(=O)NC(C(=O)OC(C(=O)NC(C(=O)N(C(C(=O)OC1)CC(C)C)C)C(C)C)C(C)C)CC(C)C)C(C)C
• Description: Sporidesmolide is a depsipeptide originally isolated from S. bakeri that has no activity against a variety of bacteria and fungi.
• Uses: Sporidesmolide I is the most polar of N-methyl analogues belonging the hexadepsipeptide sporidesmolide complex. Biosynthesis of sporidesmolide I involves the use of D- and L- amino acids utilising two leucine and four valine sub-units, where two of the valines are converted to the corresponding valic acid. The biological activity of sporidesmolide I has not been extensively investigated.

Technology Process of cyclo[DL-Leu-DL-OVal-DL-Val-DL-N(Me)Leu-Unk-DL-Val]

There total 1 articles about cyclo[DL-Leu-DL-OVal-DL-Val-DL-N(Me)Leu-Unk-DL-Val] which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ Sporidesmolid I (2900-38-1)

Guidance literature:

Hydrobromid d.D-Valyl-D-leucyl-L-α-hydroxy-isovaleryl-L-valyl-N-methyl-L-leucyl-L-α-hydroxy-isovaleriansaeure (XVIII),Thinylchlorid (20grad) 1) in CH2Cl2,Triaethylaminin in Bzl.(20grad);

DOI:10.1016/S0040-4020(01)99354-8

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