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138091-52-8

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138091-52-8 Usage

Molecular Weight

344.41 g/mol

Structure

A synthetic peptide compound derived from Tuftsin

Functionality

Potential anxiolytic and anti-depressant effects

Mechanism of Action

Modulates the expression of serotonin and dopamine in the brain

Applications

Researched for enhancing cognitive function, improving mood, and treating anxiety disorders and other psychiatric conditions

Chemical Class

Peptide compound

Appearance

Not specified in the provided material

Solubility

Not specified in the provided material

Stability

Not specified in the provided material

Reactivity

Not specified in the provided material

Safety

Not specified in the provided material

Storage

Not specified in the provided material

Purity

Not specified in the provided material

Synonyms

Not specified in the provided material

EINECS Number

Not specified in the provided material

PubChem CID

Not specified in the provided material

Check Digit Verification of cas no

The CAS Registry Mumber 138091-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,0,9 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138091-52:
(8*1)+(7*3)+(6*8)+(5*0)+(4*9)+(3*1)+(2*5)+(1*2)=128
128 % 10 = 8
So 138091-52-8 is a valid CAS Registry Number.

138091-52-8Relevant articles and documents

TRIAZA-SPIRODECANONES AS DDR1 INHIBITORS

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Page/Page column 78, (2017/01/26)

The present invention relates to compounds of formula (I) or pharmaceutically acceptable salts thereof, wherein L and R1 to R5 are as described herein, as well as processes for their manufacture, pharmaceutical compositions comprising them, and their use as medicaments.

TRICYCLIC SPIROCYCLE DERIVATIVES AND METHODS OF USE

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Page/Page column 30, (2011/07/29)

The present invention relates to novel Tricyclic Spirocycle Derivatives, pharmaceutical compositions comprising the Tricyclic Spirocycle Derivatives and the use of these compounds for treating or preventing allergy, an allergy-induced airway response, congestion, a cardiovascular disease, an inflammatory disease, a gastrointestinal disorder, a neurological disorder, a metabolic disorder, obesity or an obesity-related disorder, diabetes, a diabetic complication, impaired glucose tolerance or aired fasting glucose.

Synthesis and characterization of selective dopamine D2 receptor antagonists. 2. Azaindole, benzofuran, and benzothiophene analogs of L-741,626

Vangveravong, Suwanna,Taylor, Michelle,Xu, Jinbin,Cui, Jinquan,Calvin, Wesley,Babic, Sonja,Luedtke, Robert R.,MacH, Robert H.

experimental part, p. 5291 - 5300 (2010/09/09)

A series of indole, 7-azaindole, benzofuran, and benzothiophene compounds have been prepared and evaluated for affinity at D2-like dopamine receptors. These compounds share structural elements with the classical D 2-like dopamine rec

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