Target intelligence / Profile preview

Cerastes cerastes venom (CCV)

Target
CCV
Molecular classification
Snake venom metalloproteinase (SVMP), Phospholipase A2 (PLA2), Snake venom serine protease (SVSP), Disintegrin, C-type lectin-like protein (Snaclec), L-amino acid oxidase (LAAO)
01

Overview

Cerastes cerastes venom is a complex biochemical mixture of proteins and peptides produced by the Saharan Horned Viper, primarily utilized for prey immobilization and digestion. The venom is characterized by its potent hemotoxic and cytotoxic properties, which are largely driven by enzymes such as snake venom metalloproteinases (SVMPs), phospholipases A2 (PLA2s), and serine proteases (Fahmi et al., 2012). These components act synergistically to disrupt the vascular endothelium, degrade the extracellular matrix, and interfere with the coagulation cascade, leading to local edema, systemic hemorrhage, and consumptive coagulopathy (Casewell et al., 2015). Additionally, the venom contains non-enzymatic proteins like disintegrins that inhibit platelet aggregation by binding to integrin receptors, further exacerbating bleeding risks. While the venom is the primary agent of pathology in snakebite envenomation, its individual constituents are of significant interest in drug discovery for developing novel anticoagulants and anti-cancer agents. Clinical management of envenomation requires the rapid administration of antivenoms, which consist of purified antibodies designed to neutralize the diverse toxic proteins within the venom (WHO, 2021).

Other names
Saharan Horned Viper venomHorned Desert Viper venomCerastes cerastes snake venom
02

Mechanism of action

Passive immunization via polyvalent or monovalent antivenom containing F(ab')2 or Fab antibody fragments that bind and neutralize specific venom toxins, such as metalloproteinases and phospholipases, preventing their interaction with host tissues and coagulation factors (WHO, 2021).

03

Biological functions

ProteolysisHemolysisPlatelet aggregation inhibitionAnticoagulationCytotoxicityExtracellular matrix degradation
04

Disease associations

Snakebite envenomationHemorrhageConsumptive coagulopathyLocal tissue necrosisThrombocytopenia
05

Safety considerations

AnaphylaxisSerum sicknessAcute kidney injury (secondary to envenomation)Permanent tissue loss due to dermonecrosis
06

Interacting drugs

Fav-Afrique

3 more in the full profile.

07

Biomarkers

Prothrombin time (PT)Partial thromboplastin time (PTT)Fibrinogen levelPlatelet countCreatine kinase (CK)

Beyond the preview

Go deeper on Cerastes cerastes venom (CCV).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Cerastes cerastes venom (CCV).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call