Complement System

The complement system is a sophisticated part of the immune system that enhances the ability of antibodies and phagocytic cells to clear microbes and damaged cells, promotes inflammation, and attacks the pathogen's cell membrane. This system is named for its capacity to "complement" the killing of pathogens by antibodies.

Comprising over 30 small proteins produced by the liver, the complement system circulates in the blood serum and within tissues throughout the body. These proteins are normally inactive but become sequentially activated in response to a pathogen. Activation can occur via three pathways: the classical pathway, which is triggered by antibodies bound to a pathogen; the lectin pathway, which is activated by mannose-binding lectin attaching to the pathogen surface; and the alternative pathway, which can be initiated directly by pathogen surfaces.

Each pathway leads to the cleavage of the protein C3, generating C3a and C3b fragments. C3b binds to the pathogen surface and can lead to direct opsonization—tagging the pathogen for destruction by phagocytes. C3a, along with other small fragments released during complement activation, acts as a chemoattractant to recruit immune cells to the site of infection and promote inflammation.

The final common step of the complement activation pathways is the assembly of the membrane attack complex (MAC). This complex forms a pore in the membrane of the target cell, leading to cell lysis and death. The MAC is particularly effective against gram-negative bacteria.

Regulation of the complement system is crucial, as overactivation can damage host cells. Regulators are present in blood plasma and on cell surfaces, ensuring the system is directed only at pathogens or damaged cells.

The complement system plays a crucial role not only in innate immunity but also as a bridge to adaptive immunity. It assists in clearing immune complexes and apoptotic cells, and in enhancing the humoral response and immune memory.

Understanding and manipulating the complement system has therapeutic potential for numerous diseases, including those that involve excessive or inappropriate activation of the complement pathways.

20 Items

  • Dexamethasone
    Cat. No.
    A10299

    Dexamethasone

    Synonyms: Decadron

    Dexamethasone is a potent synthetic member of the glucocorticoid class of steroid drugs. It acts as an anti-inflammatory and immunosuppressant. Its potency is about 20-30 times that of the naturally occurring hormone hydrocortisone and 4-5 times of prednisone.

    50 mg
    $20.00
    100 mg
    $25.00
    All 6 sizes
  • PMX-205
    Cat. No.
    A16946

    PMX-205

    PMX-205 is a cyclic hexapeptide that acts as a potent antagonist of C5a receptor (C5aR; IC50 = 31 nM).

    1 mg
    $70.00
    2 mg
    $120.00
    All 7 sizes
  • Dexamethasone acetate
    Cat. No.
    A16494

    Dexamethasone acetate

    Synonyms: Dexamethasone 21-acetate; Hexadecadrol acetate

    Dexamethasone acetate (Dexamethasone 21-acetate) is a glucocorticoid receptor agonist.

    500 mg
    $40.00
    1 g
    $70.00
    All 4 sizes
  • Dexamethasone palmitate
    Cat. No.
    A18453

    Dexamethasone palmitate

    Synonyms: Limethason; Dexamethasone 21-palmitate

    Dexamethasone palmitate (DXP) is a prodrug of Dexamethasone, which is a glucocorticoid receptor agonist. Dexamethasone palmitate (DXP) has a 47-fold lower affinity for the glucocorticoid receptor than Dexamethasone. Anti-inflammatory agent.

    5 mg
    $20.00
    10 mg
    $35.00
    All 7 sizes
  • JR14a
    Cat. No.
    A24350

    JR14a

    JR14a is a potent thiophene-based antagonist of the human complement C3a receptor (C3aR). It exhibits high selectivity for C3aR over the C5a receptor and effectively suppresses C3aR-mediated inflammatory responses. JR14a is a valuable tool for studying the role of C3aR in immune regulation and inflammation-related diseases.

    5 mg
    $198.00
    10 mg
    $341.00
    All 4 sizes
  • ADH-503
    Cat. No.
    A24351

    ADH-503

    Synonyms: (Z)-Leukadherin-1 choline

    ADH-503 ((Z)-Leukadherin-1 choline) is an orally active, allosteric agonist of CD11b, an integrin subunit expressed on myeloid cells. By activating CD11b, ADH-503 promotes the repolarization of tumor-associated macrophages (TAMs) toward a pro-inflammatory phenotype, reduces the infiltration of immunosuppressive myeloid cells into tumors, and enhances dendritic cell responses. These immunomodulatory effects support its potential use in cancer immunotherapy.

    5 mg
    $45.00
    10 mg
    $78.00
    All 4 sizes
  • L-156602
    Cat. No.
    A24465

    L-156602

    Synonyms: Antibiotic L 156602; PD 124966

    L-156602 is a C5a receptor antagonist that inhibits inflammation and blocks the migration of monocytes and neutrophils to sites of infiltration in mouse inflammatory models. It also suppresses the efferent phase of delayed-type hypersensitivity (DTH).

    1 mg
    $720.00
    5 mg
    $2,160.00
    All 4 sizes
  • CP-447697
    Cat. No.
    A24469

    CP-447697

    CP-447697 is a lipophilic C5a receptor antagonist with an IC₅₀ value of 31 nM. It is suitable for research related to inflammation and complement system modulation.

    5 mg
    $72.00
    10 mg
    $124.00
    All 4 sizes
  • BM213
    Cat. No.
    A24475

    BM213

    BM213 is a potent and selective agonist of C5aR1 that demonstrates antitumor activity in a mouse model of mammary carcinoma.

    5 mg
    $90.00
    10 mg
    $155.00
    All 4 sizes
  • C3a receptor agonist 1
    Cat. No.
    A24478

    C3a receptor agonist 1

    C3a Receptor Agonist 1 (a benzeneacetamide derivative) is a potent agonist of the C3a receptor. It holds potential for research in acute inflammation and complement system–mediated responses.

    1 mg
    $81.00
    5 mg
    $243.00
    All 4 sizes
  • W-54011
    Cat. No.
    A24479

    W-54011

    W-54011 is a potent, orally active, non-peptide antagonist of the C5a receptor. It inhibits the binding of \[¹²⁵I]-labeled C5a to human neutrophils with a Kᵢ of 2.2 nM. W-54011 also suppresses C5a-induced intracellular Ca²⁺ mobilization, chemotaxis, and reactive oxygen species (ROS) generation in human neutrophils, with IC₅₀ values of 3.1 nM, 2.7 nM, and 1.6 nM, respectively.

    1 mg
    $45.00
    5 mg
    $135.00
    All 4 sizes
  • JPE-1375
    Cat. No.
    A24484

    JPE-1375

    JPE-1375 is a complement C5a receptor 1 (C5aR1) antagonist that effectively inhibits polymorphonuclear leukocyte mobilization with an EC₅₀ of 6.9 µM and reduces TNF levels with an EC₅₀ of 4.5 µM in mice. It is suitable for research in autoimmune and inflammatory diseases.

    5 mg
    $108.00
    10 mg
    $186.00
    All 4 sizes
  • C5a Receptor agonist, W5Cha
    Cat. No.
    A35186

    C5a Receptor agonist, W5Cha

    C5a Receptor agonist, W5Cha, is a selective agonist of the complement C5a receptor (C5aR), exhibiting an EC50 of 0.2 μM. This hexapeptide is derived from the C-terminus of C5a and features specific amino acid modifications that enhance its bioactivity. W5Cha effectively activates the C5aR by interacting with the Arg-206 site, making it a valuable tool for studying C5aR-mediated signaling pathways and related biological processes in inflammatory responses.

    5 mg
    $80.00
    10 mg
    $125.00
    All 2 sizes
  • (Trp63,Trp64)-C3a(63-77)
    Cat. No.
    A35196

    (Trp63,Trp64)-C3a(63-77)

    (Trp63,Trp64)​-​C3a(63-77) is a synthetic analogue of the complement component C3a, acting as a potent C3a receptor agonist. This peptide demonstrates robust calcium-stimulating activity in human neutrophils and rat basophilic leukemia (RBL-2H3) cells expressing the human and mouse C3a receptors, with EC50 values of 9.5 nM, 2.0 nM, and 0.8 nM, respectively. It is valuable for studies exploring immune response modulation and related signaling pathways.

    1 mg
    $190.00
    5 mg
    $485.00
    All 3 sizes
  • C5aR1 antagonist 1
    Cat. No.
    A35207

    C5aR1 antagonist 1

    C5aR1 antagonist 1 is a selective antagonist of the complement component 5a receptor 1 (C5aR1) with notable oral bioavailability. It exhibits potent activity in both DISCO and migration assays, demonstrating IC50 values of 38 nM and 17 nM, respectively. This compound is suitable for investigating the roles of C5aR1 in acute and chronic inflammatory diseases, facilitating research into potential therapeutic interventions.

    Out of stock

    All 3 sizes
  • Izicopan
    Cat. No.
    A35216

    Izicopan

    Synonyms: INF056

    Izicopan (INF056) is a potent antagonist of the complement factor C5a receptor, effectively disrupting C5a-mediated signaling pathways. It demonstrates significant inhibition of C5a-induced calcium mobilization, with an IC50 in the range of 10-100 nM. This compound is valuable for research into inflammatory responses and immune modulation, making it a crucial tool for studies focused on autoimmune diseases and related therapeutic interventions.

    Out of stock

    All 3 sizes
  • C5aR1 antagonist 2
    Cat. No.
    A35227

    C5aR1 antagonist 2

    C5aR1 antagonist 2 is an orally active antagonist targeting the C5a receptor 1 (C5aR1). It effectively inhibits C5a-induced neutrophil recruitment, demonstrated by IC50 values of 21 nM in DISCO assays and 3 nM in migration assays. This compound is suitable for research into acute and chronic inflammatory diseases, providing a valuable tool for understanding the role of C5aR1 in inflammatory processes.

    Out of stock

    All 3 sizes
  • ACT-1014-6470
    Cat. No.
    A35232

    ACT-1014-6470

    ACT-1014-6470 is a selective and reversible antagonist of the C5a receptor 1 (C5aR1). It exhibits strong inhibitory activity against C5aR1 activation, making it a valuable tool for investigating inflammatory processes. This compound is suitable for research applications related to various inflammatory diseases, providing insights into the role of C5aR1 in immune responses.

    Out of stock

    All 3 sizes

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