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Complement C1s

Complement C1s Informations sur la molécule

Nom anglaisComplement C1sNombre de médicaments commercialisés4
Nombre de médicaments cliniques5Alias de la cibleEC:3.4.21.42,EC 3.4.21,C1 esterase,Complement component 1 subcomponent s,C1S,Complement C1s,Complement Component 1, S Subcomponent,Basic Proline-Rich Peptide IB-1,Complement C1s Subcomponent,EC 3.4.21.42,EDSPD2
Phase de R&D la plus avancéeApproved
Nom anglaisComplement C1s
Alias de la cibleEC:3.4.21.42,EC 3.4.21,C1 esterase,Complement component 1 subcomponent s,C1S,Complement C1s,Complement Component 1, S Subcomponent,Basic Proline-Rich Peptide IB-1,Complement C1s Subcomponent,EC 3.4.21.42,EDSPD2
Nombre de médicaments commercialisés4
Nombre de médicaments cliniques5
Phase de R&D la plus avancéeApproved

Complement C1s Liste de produits

  • Attribut

    Protein (2)

  • Bibliothèque de produits

    En ligne (2)

  • Espèces

    Human (1)Cynomolgus (1)

  • Étiquette

    His Tag (2)

  • Marqueur

    Unconjugated (2)

Numéro de produitEspècesSystème d'expressionDescription du produitStructure protéiquePuretéCaractéristiquesPré-commande/Commande
COS-H52H3
Human
HEK293
Human Complement C1s Protein, His Tag, low endotoxin (MALS verified)
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COS-C52H3
Cynomolgus
HEK293
Cynomolgus Complement C1s Protein, His Tag (MALS verified)
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Quantité totale2
  • 1

Complement C1sContexte de la molécule

This gene encodes a serine protease, which is a major constituent of the human complement subcomponent C1. C1s associates with two other complement components C1r and C1q in order to yield the first component of the serum complement system. Defects in this gene are the cause of selective C1s deficiency.

Complement C1sAlias de la molécule

EDSPD2

Informations sur les médicaments cliniques

Nom anglaisCode de recherchePhase de R&DEntrepriseIndicationEssai clinique
Complement-C1 inhibitor protein (Octapharma)Phase 3 ClinicalOctapharmaAngioedemas, Hereditary
Details
RiliprubartBIVV-020; SAR-445088; TNT-020Phase 3 ClinicalTrue North TherapeuticsAnemia, Hemolytic, Autoimmune; Graft Rejection; Nervous System Diseases; Polyradiculoneuropathy; Polyradiculoneuropathy, Chronic Inflammatory Demyelinating; Purpura, Thrombocytopenic, Idiopathic
Details
C1 esterase inhibitor (Boya Bio-Pharmaceutical)Phase 3 ClinicalBoya Bio-Pharmaceutical Group Co LtdAngioedemas, Hereditary
Details
ClaseprubartDNTH103; DNTH-103Phase 3 ClinicalDianthus Therapeutics IncAutoimmune Diseases; Motor Neuron Disease; Multifocal Motor Neuropathy; Myasthenia Gravis; Nervous System Diseases; Polyradiculoneuropathy; Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Details
C1 esterase inhibitor (Chengdu Institute of Biological Products)Phase 1 ClinicalChengdu Institute Of Biological Products Co LtdAngioedemas, Hereditary
Details

Informations sur les médicaments commercialisés

Nom anglaisCode de recherchePhase de R&DEntreprisePlus ancien nom de marquePays d'approbation le plus ancienIndication la plus ancienneSociété d'approbation la plus ancienneDate d'approbation la plus ancienneIndicationEssai clinique
Conestat alfarhC1-INHApprovedPharming Group NvRhucin, Esterasine, RuconestEUAngioedemas, HereditaryPharming Group Nv2010-10-28Angioedema; Angioedemas, Hereditary; Coronavirus Disease 2019 (COVID-19); Coronavirus Infections; Fatigue Syndrome, Chronic; Genetic Diseases, Inborn; Graft Rejection; Non-ST Elevated Myocardial Infarction; Rejection of renal transplantation; Renal Insufficiency
Details
SutimlimabBIVV-009; TNT-009ApprovedTrue North TherapeuticsENJAYMOUnited StatesAnemia, Hemolytic, AutoimmuneRecordati Rare Diseases Inc2022-02-04Anemia, Hemolytic, Autoimmune; Clostridium Infections; Hemolysis; Kidney Failure, Chronic; Pemphigoid, Bullous; Purpura, Thrombocytopenic, Idiopathic
Details
Complement C1 inhibitor protein (Shire ViroPharma)C1 INH-nf; C1-INH; SHP-616ApprovedSanquin Plasma Products BvCinryze, CetorUnited StatesAngioedemas, Hereditarynull2008-10-10Angioedemas, Hereditary; Brain Injuries, Traumatic; Graft Rejection; Rejection of organ transplantation
Details
C1 esterase inhibitor (Human, CSL Behring)BI-3.012; CSL-830; CSL-842; CE-1145ApprovedCsl Behring LlcBerinert, Haegarda, Berinert 2000JapanAngioedemas, HereditaryCsl Behring Llc1990-06-29Angioedemas, Hereditary; Hereditary Angioedema Types I and II; Rejection of renal transplantation
Details
  • Informations sur la molécule
  • Liste de produits
  • Informations sur les médicaments commercialisés
  • Informations sur les médicaments cliniques