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74885-72-6

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74885-72-6 Usage

Uses

5-Carboxamidotryptamine Maleate Salt Hemiethanolate is a serotonin receptors agonist. Also, it is a 5-HT1A receptor agonists causing cardiovascular effects.

Biochem/physiol Actions

Agonist at 5-HT1A, 5-HT1B, 5-HT1D, 5-HT5 and 5-HT7 serotonin receptors.

Check Digit Verification of cas no

The CAS Registry Mumber 74885-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,8 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74885-72:
(7*7)+(6*4)+(5*8)+(4*8)+(3*5)+(2*7)+(1*2)=176
176 % 10 = 6
So 74885-72-6 is a valid CAS Registry Number.

74885-72-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Sigma

  • (C117)  5-Carboxamidotryptamine maleate salt  powder, ≥98% (HPLC)

  • 74885-72-6

  • C117-5MG

  • 2,533.05CNY

  • Detail
  • Sigma

  • (C117)  5-Carboxamidotryptamine maleate salt  powder, ≥98% (HPLC)

  • 74885-72-6

  • C117-25MG

  • 9,412.65CNY

  • Detail

74885-72-6Downstream Products

74885-72-6Relevant articles and documents

Indole compounds and use thereof

-

, (2008/06/13)

Compounds are disclosed of general formula (I): STR1 wherein R1 and R2 each independently represents a hydrogen atom, or an aryl, aralkyl, cycloalkyl, fluoroalkyl or alkyl group, which alkyl group is optionally substituted by an alkenyl group or by a group -OR7 or by STR2 where R7 and R8 each independently represents a hydrogen atom, an alkyl, aryl or aralkyl group; or R1 and R2 together with the nitrogen atom to which they are attached form a saturated monocyclic 5 to 7 membered ring which may contain a further hetero function (viz--O--, --NH or STR3 R3 and R4 have the same meanings as R1 and R2 and may together form an aralkylidene group; R5 represents a hydrogen atom or an alkyl or aralkyl group; R6 represents a hydrogen atom or an aryl or C1 -C3 alkyl group; Alk represents an C1 -C4 alkylene group optionally substituted at one or more of its carbon atoms by one to three C1 -C3 alkyl groups; and X represents an oxygen or sulphur atom, and its physiologically acceptable salts, hydrates and bioprecursors. The indoles (I) may be prepared by combinations of reactions to introduce the desired substituents into suitable intermediates either before or after cyclization to form the indole nucleus. The compounds have selective actions on blood vessels and, in particular exhibit antihypertensive properties. They may be formulated in conventional manner as pharmaceutical compositions.

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