CAS 14328-51-9

Acido (αS)-α-aminocicloesanoacetico

Descrizione:

Acido (αS)-α-aminocicloesanoacetico, noto anche come L-α-amino-α-cicloesanoacetico, è un derivato degli amminoacidi caratterizzato dalla sua struttura ad anello di cicloesano. Questo composto presenta un gruppo amminico (-NH2) e un gruppo acido carbossilico (-COOH), che sono gruppi funzionali tipici presenti negli amminoacidi. La presenza dell'anello di cicloesano contribuisce alle sue uniche proprietà steriche ed elettroniche, influenzando la sua reattività e le interazioni con i sistemi biologici. È una molecola chirale, con la designazione (αS) che indica la stereochimica specifica al carbonio alfa. Questa stereochimica può influenzare significativamente la sua attività biologica e le interazioni con enzimi e recettori. Il composto è di interesse nella ricerca farmaceutica, in particolare nello sviluppo di farmaci che mirano a vie biologiche specifiche. La sua solubilità in acqua e solventi organici può variare, influenzando la sua formulazione e applicazione in vari contesti chimici e biologici. In generale, Acido (αS)-α-aminocicloesanoacetico è un composto prezioso sia in chimica sintetica che medicinale.

Formula: C₈H₁₅NO₂

InChI: InChI=1S/C8H15NO2/c9-7(8(10)11)6-4-2-1-3-5-6/h6-7H,1-5,9H2,(H,10,11)/t7-/m0/s1

InChI key: InChIKey=WAMWSIDTKSNDCU-ZETCQYMHSA-N

SMILES: [C@H](C(O)=O)(N)C1CCCCC1

Sinonimi:

• (1-Ammoniocyclohexyl)Acetate
• (2S)-2-Amino-2-cyclohexylacetic acid
• (2S)-2-Amino-2-cyclohexylethanoic acid
• (2S)-amino(cyclohexyl)ethanoic acid
• (S)-2-Amino-2-cyclohexylacetic acid
• (S)-2-Cyclohexylglycine
• (αS)-α-Aminocyclohexaneacetic acid
• <span class="text-smallcaps">L</span>-Cyclohexylglycine
• <span class="text-smallcaps">L</span>-α-Cyclohexylglycine
• Amino(Cyclohexyl)Acetic Acid
• Cyclohexaneacetic acid, α-amino-, (S)-
• Cyclohexaneacetic acid, α-amino-, (αS)-
• Cyclohexaneacetic acid, α-amino-, <span class="text-smallcaps">L</span>-
• H-Chg-OH
• L-(+)-2-Cyclohexylglycine
• L-Cyclohexyglycine
• L-Cyclohexyl glycine
• L-alpha-Cyclohexylglycine
• Cyclohexaneacetic acid, α-amino-, L-
• L-α-Cyclohexylglycine
• L-2-CYCLOHEXYLGLYCINE HYDROCHLORIDE
• L-CYCLOHEXYLGLYCINE 98%
• H-L-Chg-OH*HCl
• H-CHG-OH HCL
• L-a-cyclobenzyl glycine
• H-PHG(HEXAHYDRO)-OH HCL
• L-2-CYCLOHEXYLGLYCINE TRIFLUOROACETATE
• HEXAHYDRO-L-PHENYLGLYCINE HYDROCHLORIDE
• H-Cyclohexyl-Gly-OH (H-Chg-OH: L-2-Cyclohexylglycine)
• H-CYCLOHEXYL-GLY-OH HCL
• L-ALPHA-CYCLOHEXYLGLYCINE HYDROCHLORIDE SALT
• L-ALPHA-CYCLOHEXYLGYCINE HYDROCHLORIDE SALT
• H-CHG-OH TFA
• H-CYCLOHEXYL-GLY-OH TFA
• L-CYCLOHEXYLGLYCINE HYDROCHLORIDE
• (S)-CYCLOHEXYLGLYCINE HCL

L-2-Cyclohexylglycine

CAS: 14328-51-9

Formula: C₈H₁₅NO₂

Purezza: >98.0%(T)(HPLC)

Colore e forma: White to Almost white powder to crystal

Peso molecolare: 157.21

Ref: 3B-C2569

L-(+)-2-Cyclohexylglycine, 98%

CAS: 14328-51-9

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₈H₁₅NO₂

Purezza: 98%

Colore e forma: Powder, White

Peso molecolare: 157.21

Ref: 02-H26881

H-Chg-OH

CAS: 14328-51-9

Formula: C₈H₁₅NO₂

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 157.2102

Ref: IN-DA003R6L

L-Cyclohexylglycine u3000

CAS: 14328-51-9

Formula: C₈H₁₅NO₂

Peso molecolare: 157.22

Ref: 7W-GM3629

L-(+)-2-Cyclohexylglycine

CAS: 14328-51-9

L-(+)-2-Cyclohexylglycine

Purezza: 98%

Peso molecolare: 157.21g/mol

Ref: 54-OR350213

2-Cyclohexyl-L-glycine

CAS: 14328-51-9

Formula: C₈H₁₅NO₂

Purezza: 97%

Colore e forma: Solid, Powder

Peso molecolare: 157.213

Ref: 10-F034414

L-a-Cyclohexylglycine

CAS: 14328-51-9

L-a-Cyclohexylglycine is an efficient, general method for the preparation of peptide aldehydes. It is a serine protease inhibitor that binds to thrombin and prevents it from converting fibrinogen into fibrin. L-a-Cyclohexylglycine has been shown to inhibit polymerization of fibrinogen and factor XIII, as well as the formation of thrombin, which is important for blood clotting. L-a-Cyclohexylglycine also inhibits hepatitis C virus (HCV) replication in vitro by binding to the HCV NS3 helicase protein. This compound has been shown to be able to inhibit HIV-1 protease activity and may have potential use as an antiviral agent.

Formula: C₈H₁₅NO₂

Purezza: Min. 95%

Colore e forma: White Powder

Peso molecolare: 157.21 g/mol

Ref: 3D-FC43992