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Home > Encyclopedia > N,N′-(Sulfonyldi-4,1-phenylene)bis[1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinesulfonamide]

N,N′-(Sulfonyldi-4,1-phenylene)bis[1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinesulfonamide]

N,N′-(Sulfonyldi-4,1-phenylene)bis[1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinesulfonamide] structure

N,N′-(Sulfonyldi-4,1-phenylene)bis[1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinesulfonamide] 

structure
  • CAS No:

    34941-71-4

  • Formula:

    C22H20N6O10S3

  • Chemical Name:

    N,N′-(Sulfonyldi-4,1-phenylene)bis[1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinesulfonamide]

  • Synonyms:

    5-Pyrimidinesulfonamide,N,N′-(sulfonyldi-4,1-phenylene)bis[1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-;N,N′-(Sulfonyldi-4,1-phenylene)bis[1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinesulfonamide];p,p′-Bis[(2,4-dihydroxy-6-methyl-5-pyrimidinyl)sulfonamino]diphenyl sulfone;Diutsifon;Diucifone;Diuciphone

N,N′-(Sulfonyldi-4,1-phenylene)bis[1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinesulfonamide] Basic Attributes

624.6 g/mol

624.62

H2J64M9K8Z

Characteristics

268 Ų

Drug Information

Substances that augment, stimulate, activate, potentiate, or modulate the immune response at either the cellular or humoral level. The classical agents (Freund's adjuvant, BCG, Corynebacterium parvum, et al.) contain bacterial antigens. Some are endogenous (e.g., histamine, interferon, transfer factor, tuftsin, interleukin-1). Their mode of action is either non-specific, resulting in increased immune responsiveness to a wide variety of antigens, or antigen-specific, i.e., affecting a restricted type of immune response to a narrow group of antigens. The therapeutic efficacy of many biological response modifiers is related to their antigen-specific immunoadjuvanticity. (See all compounds classified as Adjuvants, Immunologic.)|Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)|Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues. (See all compounds classified as Antifungal Agents.)|Substances that suppress Mycobacterium leprae, ameliorate the clinical manifestations of leprosy, and/or reduce the incidence and severity of leprous reactions. (See all compounds classified as Leprostatic Agents.)|Drugs used to treat or prevent skin disorders or for the routine care of skin. (See all compounds classified as Dermatologic Agents.)

diucifon

Computed Properties

Molecular Weight:624.6
XLogP3:-0.9
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:8
Exact Mass:624.04030438
Monoisotopic Mass:624.04030438
Topological Polar Surface Area:268
Heavy Atom Count:41
Complexity:1420
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Guide of N,N′-(Sulfonyldi-4,1-phenylene)bis[1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinesulfonamide]

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