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Home > Encyclopedia > 7H-Furo[3,2-g][1]benzopyran-7-one, 3-[(2-aminoethoxy)methyl]-2,5,9-trimethyl-, hydrochloride (1:1)

7H-Furo[3,2-g][1]benzopyran-7-one, 3-[(2-aminoethoxy)methyl]-2,5,9-trimethyl-, hydrochloride (1:1)

7H-Furo[3,2-g][1]benzopyran-7-one, 3-[(2-aminoethoxy)methyl]-2,5,9-trimethyl-, hydrochloride (1:1) structure

7H-Furo[3,2-g][1]benzopyran-7-one, 3-[(2-aminoethoxy)methyl]-2,5,9-trimethyl-, hydrochloride (1:1) 

structure
  • CAS No:

    161262-45-9

  • Formula:

    C17H19NO4.ClH

  • Chemical Name:

    7H-Furo[3,2-g][1]benzopyran-7-one, 3-[(2-aminoethoxy)methyl]-2,5,9-trimethyl-, hydrochloride (1:1)

  • Synonyms:

    7H-Furo[3,2-g][1]benzopyran-7-one,3-[(2-aminoethoxy)methyl]-2,5,9-trimethyl-,hydrochloride (1:1);7H-Furo[3,2-g][1]benzopyran-7-one,3-[(2-aminoethoxy)methyl]-2,5,9-trimethyl-,hydrochloride;Amotosalen hydrochloride;S 59;(2-Amino-ethoxymethyl)-2,5,9-trimethyl-furo[3,2-g]chromen-7-one hydrochloride

Description

Amotosalen Hydrochloride is the hydrochloride salt form of amotosalen, a synthetic psoralen and light-activated DNA, RNA crosslinking agent, with protective activity against pathogens such as bacteria, viruses, protozoa, and leukocytes. Prior to administration amotosalen is added to plasma and platelets, then in vivo the agent penetrates pathogens and targets DNA and RNA. Upon activation by ultraviolet A light, this agent is able to form interstrand DNA and RNA crosslinks and prevents replication. Inactivation of leukocytes can prevent graft versus host disease upon transfusion.

7H-Furo[3,2-g][1]benzopyran-7-one, 3-[(2-aminoethoxy)methyl]-2,5,9-trimethyl-, hydrochloride (1:1) Basic Attributes

337.79800

337.1080858 g/mol

67B255SI5F

DTXSID70167093

C72699

Characteristics

78.60000

4.44200

488.8ºC

249.4ºC

1.06E-09mmHg at 25°C

Safety Information

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P272, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P333+P313, P337+P313, P362, P363, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Drug Information

Drugs used to treat or prevent skin disorders or for the routine care of skin. (See all compounds classified as Dermatologic Agents.)|Drugs that are pharmacologically inactive but when exposed to ultraviolet radiation or sunlight are converted to their active metabolite to produce a beneficial reaction affecting the diseased tissue. These compounds can be administered topically or systemically and have been used therapeutically to treat psoriasis and various types of neoplasms. (See all compounds classified as Photosensitizing Agents.)

amotosalen

Computed Properties

Molecular Weight:337.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:337.1080858
Monoisotopic Mass:337.1080858
Topological Polar Surface Area:74.7
Heavy Atom Count:23
Complexity:464
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Guide of 7H-Furo[3,2-g][1]benzopyran-7-one, 3-[(2-aminoethoxy)methyl]-2,5,9-trimethyl-, hydrochloride (1:1)

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