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4-(4-Bromo-3-methylphenyl)-1,2,3,6-tetrahydropyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

227305-00-2

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227305-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 227305-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,3,0 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 227305-00:
(8*2)+(7*2)+(6*7)+(5*3)+(4*0)+(3*5)+(2*0)+(1*0)=102
102 % 10 = 2
So 227305-00-2 is a valid CAS Registry Number.

227305-00-2Upstream product

227305-00-2Downstream Products

227305-00-2Relevant academic research and scientific papers

Metalloprotease inhibitors

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, (2008/06/13)

Compounds of formula (I) and pharmaceutically-acceptable derivatives thereof, are matrix metalloprotease inhibitors, useful in treatment of conditions mediated by matrix metalloproteases, such as chronic dermal ulcers.

Composition for the treatment of damaged tissue

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, (2008/06/13)

A pharmaceutical for use in damaged tissue, such as wound, treatment (e.g. healing) is described. The pharmaceutical comprising a composition which comprises: (a) a growth factor; and (b) an inhibitor agent; and optionally (c) a pharmaceutically acceptable carrier, diluent or excipient; wherein the inhibitor agent can inhibit the action of at least one specific adverse protein (e.g. a specific protease) that is upregulated in a damaged tissue, such as a wound, environment.

Hydroxamic acid derivatives as matrix metalloprotease (MMP) inhibitors

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, (2008/06/13)

Compounds of formula (I):or pharmaceutically or veterinarily acceptable salts thereof, or pharmaceutically or veterinarily acceptable solvates of either entity, wherein the broken line represents an optional bond; A is C or CH; B is CH2, O or absent; R1 and R2 are each independently selected from hydrogen, C1 to C6 alkyl optionally substituted with C1 to C4 alkoxy or phenyl, and C1 to C6 alkenyl; or, together with the carbon atom to which they are attached, form a C3 to C6 cycloalkyl group which optionally incorporates a heteroatom linkage selected from O, SO, SO2 and NR6 or which is optionally benzo-fused; R3 is hydrogen, halo, R7 or OR7; R4 is hydrogen, C1 to C4 alkyl, C1 to C4 alkoxy, trifluoromethyl or halo; R6 is hydrogen or C1 to C4 alkyl; R7 is an optionally substituted monocyclic or bicyclic ring system; m is 1 or 2; and n is 0, 1 or 2; with the proviso that B is not O when A is C; are MMP inhibitors useful in the treatment of, inter alia, tissue ulceration, wound repair and skin diseases.

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