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H-Thr(Bzl)-OBzl·HCl, also known as N-benzyloxycarbonyl-L-threonine hydrochloride, is a chemical compound derived from threonine, an essential amino acid. It is utilized in peptide synthesis and drug development, featuring a benzyloxycarbonyl (Bzl) group that protects the threonine molecule from unwanted reactions. The hydrochloride salt form enhances its solubility and stability in aqueous solutions, making it a valuable component in the preparation of peptide-based drugs and pharmaceuticals.

67580-86-3

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67580-86-3 Usage

Uses

Used in Pharmaceutical Industry:
H-Thr(Bzl)-OBzl·HCl is used as a protecting agent for threonine residues during peptide synthesis for the development of peptide-based drugs. The benzyloxycarbonyl group ensures that the threonine molecule remains protected from unwanted reactions, allowing for selective modification and protection in synthesized peptides.
Used in Drug Development:
H-Thr(Bzl)-OBzl·HCl is employed as a key component in the synthesis of pharmaceuticals, particularly those that require the incorporation of threonine residues. Its ability to selectively modify and protect these residues contributes to the successful development of effective peptide-based therapeutics.
Used in Peptide Synthesis:
H-Thr(Bzl)-OBzl·HCl is used as a building block in the synthesis of peptides, providing a protected form of threonine that can be selectively deprotected and incorporated into the desired peptide sequence. This selective protection is crucial for the successful synthesis of complex peptide structures with specific biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 67580-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,8 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67580-86:
(7*6)+(6*7)+(5*5)+(4*8)+(3*0)+(2*8)+(1*6)=163
163 % 10 = 3
So 67580-86-3 is a valid CAS Registry Number.

67580-86-3Relevant academic research and scientific papers

SPIRO-LACTAM NMDA RECEPTOR MODULATORS AND USES THEREOF

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Page/Page column 39, (2019/08/26)

Disclosed are compounds having potency in the modulation of NMDA receptor activity. Such compounds can be used in the treatment of conditions such as depression and related disorders as well as other disorders.

SPIRO-LACTAM AND BIS-SPIRO-LACTAM NMDA RECEPTOR MODULATORS AND USES THEREOF

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Page/Page column 100, (2018/03/28)

Disclosed are compounds having potency in the modulation of NMDA receptor activity. Such compounds can be used in the treatment of conditions such as depression and related disorders. Orally delivered formulations and other pharmaceutically acceptable delivery forms of the compounds, including intravenous formulations, are also disclosed.

SPIRO-LACTAM NMDA MODULATORS AND METHODS OF USING SAME

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Page/Page column 46; 51, (2018/03/28)

Disclosed are compounds having potency in the modulation of NMDA receptor activity. Such compounds can be used in the treatment of conditions such as depression and related disorders. Orally delivered formulations and other pharmaceutically acceptable delivery forms of the compounds, including intravenous formulations, are also disclosed.

SPIRO-LACTAM NMDA RECEPTOR MODULATORS AND USES THEREOF

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Page/Page column 47, (2018/03/09)

Disclosed are compounds having potency in the modulation of NMDA receptor activity. Such compounds can be used in the treatment of conditions such as depression and related disorders. Orally delivered formulations and other pharmaceutically acceptable delivery forms of the compounds, including intravenous formulations, are also disclosed.

SPIRO-LACTAM NMDA RECEPTOR MODULATORS AND USES THEREOF

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Page/Page column 33, (2017/12/15)

Disclosed are compounds having enhanced potency in the modulation of NMDA receptor activity. Such compounds can be used in the treatment of conditions such as depression and related disorders. Orally available formulations and other pharmaceutically acceptable delivery forms of the compounds, including intravenous formulations, are also disclosed.

SPIRO-LACTAM NMDA RECEPTOR MODULATORS AND USES THEREOF

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Page/Page column 26; 32; 33, (2017/12/16)

Disclosed are compounds having enhanced potency in the modulation of NMDA receptor activity. Such compounds are contemplated for use in the treatment of conditions such as depression and related disorders. Orally available formulations and other pharmaceutically acceptable delivery forms of the compounds, including intravenous formulations, are also disclosed. Formula (I).

SPIRO-LACTAM NMDA RECEPTOR MODULATORS AND USES THEREOF

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Paragraph 0103, (2014/08/19)

Disclosed are compounds having enhanced potency in the modulation of NMDA receptor activity. Such compounds are contemplated for use in the treatment of conditions such as depression and related disorders. Orally available formulations and other pharmaceutically acceptable delivery forms of the compounds, including intravenous formulations, are also disclosed.

SPIRO-LACTAM NMDA RECEPTOR MODULATORS AND USES THEREOF

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Paragraph 0095, (2014/08/19)

Disclosed are compounds having enhanced potency in the modulation of NMD A receptor activity. Such compounds are contemplated for use in the treatment of conditions such as depression and related disorders. Orally available formulations and other pharmaceutically acceptable delivery forms of the compounds, including intravenous formulations, are also disclosed.

Total synthesis of (-)-stevastelin B

Kurosawa, Kazuo,Nagase, Toshihiko,Chida, Noritaka

, p. 1280 - 1281 (2007/10/03)

The total synthesis and an unambiguous structure confirmation of stevastelin B 1, a novel 15-membered cyclic depsipeptide, are described; the fatty acid moiety in 1, prepared stereoselectively from L-quebrachitol was converted into the amino carboxylic acid, whose macrolactamization by Shioiri's procedure effectively constructed the cyclic structure of 1.

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