41017-96-3

Basic information

• Product Name: H-ILE-VAL-OH
• Synonyms: L-ISOLEUCYL-L-VALINE;ILE-VAL;H-ILE-VAL-OH;Isoleucylvaline;L-Valine, L-isoleucyl-;(S)-2-((2S,3S)-2-amino-3-methylpentanamido)-3-methylbutanoic acid
• CAS NO: 41017-96-3
• Molecular Formula: C₁₁H₂₂N₂O₃
• Molecular Weight: 230.3
• Mol File: 41017-96-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 421.9°Cat760mmHg
• Flash Point: 209°C
• Appearance: /
• Density: 1.066g/cm³
• Vapor Pressure: 2.66E-08mmHg at 25°C
• Refractive Index: 1.482
• Storage Temp.: -15°C
• CAS DataBase Reference: H-ILE-VAL-OH(CAS DataBase Reference)
• NIST Chemistry Reference: H-ILE-VAL-OH(41017-96-3)
• EPA Substance Registry System: H-ILE-VAL-OH(41017-96-3)

Safety Data

• Hazardous Substances Data: 41017-96-3(Hazardous Substances Data)

Usage

Definition

ChEBI: A dipeptide formed from L-isoleucine and L-valine residues.

InChI:InChI=1/C11H22N2O3/c1-5-7(4)8(12)10(14)13-9(6(2)3)11(15)16/h6-9H,5,12H2,1-4H3,(H,13,14)(H,15,16)/t7-,8-,9-/m0/s1

Upstream product

• 72-18-4 L-valine 
• 5860-63-9 (S)-4-((S)-sec-butyl)oxazolidine-2,5-dione 
• 41487-00-7 N-Benzyloxycarbonyl-L-isoleucyl-L-valin 
• 3391-99-9 N-Z-L-isoleucine N-hydroxysuccinimide ester 
• 53665-97-7 Z-Ile-ONB 

Downstream Products

• 73809-01-5 Boc-GlyIleValGlu(OBut)Gln(Mbh)-OH 

Relevant articles and documents

Neopeapyran, an unusual furo[2,3b]pyran analogue and turnagainolide C from a soil Streptomyces sp. S2236

Neopeapyran (1), an unusual furo[2,3b]pyran analogue, together with a new cyclopeptide, turnagainolide C (2), were isolated from Streptomyces sp. S2236 associated with the rhizosphere soil of Panax notoginseng. The planar structure and relative configuration of neopeapyran (1) were elucidated on the basis of spectroscopic techniques, while the absolute configuration was determined by TDDFT calculation. The absolute configuration of turnagainolide C (2) was determined by partial hydrolysis, together with the advanced Marfey's method and spectroscopic analysis. The antimicrobial activities of these two compounds were also investigated.

Synthesis of N-terminal peptide fragments of the insulin A-chain

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