Cyclo(L-Phe-L-Val) - ≥99% , CAS No.35590-86-4

CAS: 35590-86-4 Cat. No.: C648410 Formula: C14H18N2O2 Peso molecolare: 246.30 PubChem CID: 13783105
Disponibile su ordine
GRADE & PURITY ≥99%
Storage
Desiccated,Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Germania (EU)
USA*
Price
Qty
5mg
C648410-5mg
Su ordinazione · 8–12 settimane
399,94€
10mg
C648410-10mg
Su ordinazione · 8–12 settimane
642,91€
25mg
C648410-25mg
Su ordinazione · 8–12 settimane
1.354,45€
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Desiccated,Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Cyclo(L-Phe-L-Val) is a potent inhibitor of enzymes isocitrate lyase ( ICL ) ( IC 50 =27 μg/mL). cyclo(L-Phe-L-Val) inhibits the gene transcription of ICL in C. albicans under C 2 -carbon-utilizing conditions

In Vitro

Cyclo(L-Phe-L-Val) (32 μg/mL; 2 d) decreases icl product in C. albicans SC5314 (wild-type), MRC10 (Δicl), and MRC11 (Δicl + ICL), respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

IC50& Target:Isocitrate lyase (ICL)

Specifications

Specifiche e purezza
≥99%
Meccanismi biochimici e fisiologici
Cyclo(L-Phe-L-Val) is a potent inhibitor of enzymes isocitrate lyase ( ICL ) ( IC 50 =27 μg/mL). cyclo(L-Phe-L-Val) inhibits the gene transcription of ICL in C. albicans under C 2 -carbon-utilizing conditions.
Condizioni di conservazione di stoccaggio
Desiccated,Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Tipo di azione
INHIBITOR
Purezza
≥99%
Nomi e identificatori
Sorrisi canonici
CC(C)C1C(=O)NC(C(=O)N1)CC2=CC=CC=C2
IUPAC Name
(3S,6S)-3-benzyl-6-propan-2-ylpiperazine-2,5-dione
InChIKey
OQQPOHUVAQPSHJ-RYUDHWBXSA-N
INCHI
1S/C14H18N2O2/c1-9(2)12-14(18)15-11(13(17)16-12)8-10-6-4-3-5-7-10/h3-7,9,11-12H,8H2,1-2H3,(H,15,18)(H,16,17)/t11-,12-/m0/s1
Isomeri SMILES
CC(C)[C@H]1C(=O)N[C@H](C(=O)N1)CC2=CC=CC=C2
PubChem CID
13783105
Peso molecolare
246.30

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives
Direct ParentAlpha amino acids and derivatives
Alternative Parents 2,5-dioxopiperazines  Benzene and substituted derivatives  Secondary carboxylic acid amides  Lactams  Azacyclic compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Alpha-amino acid or derivatives - Dioxopiperazine - 2,5-dioxopiperazine - Monocyclic benzene moiety - 1,4-diazinane - Piperazine - Benzenoid - Secondary carboxylic acid amide - Lactam - Carboxamide group - Organoheterocyclic compound - Azacycle - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteromonocyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





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Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
SolubilitàDMSO : 8.33 mg/mL (33.82 mM; ultrasonic and warming and heat to 70°C)
Peso molecolare246.300 g/mol
XLogP32.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count3
Exact Mass246.137 Da
Monoisotopic Mass246.137 Da
Topological Polar Surface Area58.200 Ų
Heavy Atom Count18
Formal Charge0
Complexity322.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calcolatori di soluzioni
Recensioni

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