You Searched For: H-D-Asp(OMe)-OH

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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tert-butoxy)-4-oxobutanoic acid ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America

Description: CAS Number: 129460-09-9
MDL Number: MFCD00065631
Molecular Formula: C23H25NO6
Molecular Weight: 411.45
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Specific rotation [a]20/D: -24 deg (C=1, DMF)

SDS

N-(tert-Butoxycarbonyl)-L-aspartic acid 98%

Supplier: Thermo Scientific Chemicals

Description: N-(tert-Butoxycarbonyl)-L-aspartic acid 98%

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Human;Mouse H-Cys-Asp-Pro-Gly-Tyr-Ile-Gly-Ser-Arg-OH Trifluoroacetate

Supplier: Bachem Americas

Description: CDPGYIGSR corresponds to residues 925-933 of the laminin B1 chain. Like the peptide amide of the same sequence (H-1224), it also binds to the laminin receptor, but with lower affinity.

Abz-Arg-Val-Lys-Arg-Gly-Leu-Ala-m-nitro-Tyr-Asp-OH Trifluoroacetate

Catalog Number: (M-2115.0001BA)

Supplier: Bachem Americas

Description: This internally quenched fluorogenic peptide substrate contains anthranilic acid as fluorescent donor and m-nitro-tyrosine as acceptor (quencher). The sequence Abz-RVKRGLAY(NO₂)E is based on the sequence of hemagglutinin. The FRET substrate is efficiently cleaved by furin, a subtilisin-like eukaryotic serine endoprotease with Km = 3.8 µM and kcat = 29.3 s⁻¹ (kcat/Km = 7'710'000 M⁻¹s⁻¹). Its kcat/Km value is over 2000-fold higher than that of the commonly used substrate Boc-Arg-Val-Arg-Arg-AMC (I-1645). FRET Substrate for the basic residue-specific yeast aspartyl protease yapsin 1.

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D-(-)-Aspartic acid ≥98.0% (by titrimetric analysis)

Catalog Number: (TCA0545-025G)

Supplier: TCI America

Description: CAS Number: 1783-96-6
MDL Number: MFCD00063081
Molecular Formula: C4H7NO4
Molecular Weight: 133.10
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Specific rotation [a]20/D: -25 deg (C=8, HCl(1+1))

SDS Certificates

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Mca-(Asn⁶⁷⁰,Leu⁶⁷¹)-Amyloid beta/A4 Protein Precursor₇₇₀ (667-675)-Lys(Dnp) Acetate

Catalog Number: (M-2420.0001BA)

Supplier: Bachem Americas

Description: Fluorogenic (FRET) substrate for pro-memapsin-2 containing the β-secretase site of the Swedish mutation of APP, SEVNLDAEF.

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Amastatin · HCl

Supplier: Bachem Americas

Description: Amastatin has originally been isolated from the culture filtrate of Streptomyces sp. ME98-M3 and is a competitive inhibitor of human serum aminopeptidase A (Ki = 1.1 · 10⁻⁶ M) and of pig kidney leucine aminopeptidase (Ki = 1.6 · 10⁻⁶ M).

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tert-butoxy)-4-oxobutanoic acid ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America

Description: CAS Number: 71989-14-5
MDL Number: MFCD00037131
Molecular Formula: C23H25NO6
Molecular Weight: 411.45
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 150
Specific rotation [a]20/D: -25 deg (C=1, DMF)

SDS Certificates

N-Methyl-D-aspartic acid ≥98%

Supplier: Thermo Scientific Chemicals

Description: Powder

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H-Cys-Arg-Gly-Asp-Phe-Pro-Ala-Ser-Ser-Cys-OH

Catalog Number: (H-2672.0001BA)

Supplier: Bachem Americas

Description: CRGDFPASSC is a cyclic RGD-containing decapeptide which binds to the fibrinogen receptor on the platelet surface. This analog with Phe substituted for Ser at position 5 was found to be 3 times more active (IC₅₀ = 2.5 µM) as a platelet aggregation inhibitor than CRGDSPASSC.

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4-Benzyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-aspartate ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America

Description: CAS Number: 86060-84-6
MDL Number: MFCD00065630
Molecular Formula: C26H23NO6
Molecular Weight: 445.47
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 127
Specific rotation [a]20/D: -20 deg (C=1, DMF)
Storage Temperature: 0-10°C

SDS

(S)-2-Amino-4-(tert-butoxy)-4-oxobutanoic acid 98%

Supplier: Thermo Scientific Chemicals

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Ac-Ser-Asp-Lys-Pro-OH

Supplier: Bachem Americas

Description: The bioactive tetrapeptide goralatide which corresponds to the N-terminus of Thymosin β₄, is a physiological regulator of hematopoiesis and inhibits the entry into the S-phase of murine and human hematopoietic stem cells. Ac-SDKP has been shown to reduce the damage to specific compartments in the bone marrow resulting from treatment with chemotherapeutic agents, ionizing radiations, hyperthermy, or phototherapy. It protects from doxorubicin-induced toxicity. Ac-SDKP is a physiological substrate of angiotensin I- converting enzyme (ACE).