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1021342-98-2

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1021342-98-2 Usage

Chemical structure

Unique, setting it apart from other antidepressant medications

Molecular weight

347.19 g/mol

Appearance

White to off-white crystalline solid

Solubility

Practically insoluble in water, slightly soluble in methanol and ethanol, and freely soluble in chloroform and acetonitrile

Mechanism of action

Affects serotonin levels in the brain, helping to improve mood, sleep, appetite, and energy levels in people with depression

Indications

Treatment of major depressive disorder

Administration

Tablet form for oral administration

Pharmacokinetics

Rapid absorption, extensive metabolism by the liver, and excretion primarily in feces

Side effects

May include nausea, diarrhea, dizziness, headache, and insomnia

Drug interactions

May interact with other medications, including other antidepressants, and should be used under the guidance of a healthcare provider.

Check Digit Verification of cas no

The CAS Registry Mumber 1021342-98-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,1,3,4 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1021342-98:
(9*1)+(8*0)+(7*2)+(6*1)+(5*3)+(4*4)+(3*2)+(2*9)+(1*8)=92
92 % 10 = 2
So 1021342-98-2 is a valid CAS Registry Number.

1021342-98-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-Isopropoxy-1-{[(2-methyl-2-propanyl)oxy]carbonyl}-1H-indol-2-y l)boronic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1021342-98-2 SDS

1021342-98-2Downstream Products

1021342-98-2Relevant articles and documents

Structurally sophisticated octahedral metal complexes as highly selective protein kinase inhibitors

Feng, Li,Geisselbrecht, Yann,Blanck, Sebastian,Wilbuer, Alexander,Atilla-Gokcumen, G. Ekin,Filippakopoulos, Panagis,Kraeling, Katja,Celik, Mehmet Ali,Harms, Klaus,Maksimoska, Jasna,Marmorstein, Ronen,Frenking, Gernot,Knapp, Stefan,Essen, Lars-Oliver,Meggers, Eric

, p. 5976 - 5986 (2011)

The generation of synthetic compounds with exclusive target specificity is an extraordinary challenge of molecular recognition and demands novel design strategies, in particular for large and homologous protein families such as protein kinases with more than 500 members. Simple organic molecules often do not reach the necessary sophistication to fulfill this task. Here, we present six carefully tailored, stable metal-containing compounds in which unique and defined molecular geometries with natural-product-like structural complexity are constructed around octahedral ruthenium(II) or iridium(III) metal centers. Each of the six reported metal compounds displays high selectivity for an individual protein kinase, namely GSK3α, PAK1, PIM1, DAPK1, MLCK, and FLT4. Although being conventional ATP-competitive inhibitors, the combination of the unusual globular shape and rigidity characteristics, of these compounds facilitates the design of highly selective protein kinase inhibitors. Unique structural features of the octahedral coordination geometry allow novel interactions with the glycine-rich loop, which contribute significantly to binding potencies and selectivities. The sensitive correlation between metal coordination sphere and inhibition properties suggests that in this design, the metal is located at a "hot spot" within the ATP binding pocket, not too close to the hinge region where globular space is unavailable, and at the same time not too far out toward the solvent where the octahedral coordination sphere would not have a significant impact on potency and selectivity. This study thus demonstrates that inert (stable) octahedral metal complexes are sophisticated structural scaffolds for the design of highly selective chemical probes.

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