Caspase 1 | C14: Caspase | IUPHAR Guide to IMMUNOPHARMACOLOGY

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Caspase 1

Target id: 1617

Nomenclature: Caspase 1

Family: C14: Caspase

Annotation status:  image of an orange circle Annotated and awaiting review. Please contact us if you can help with reviewing.  » Email us

   GtoImmuPdb view: ON :     Caspase 1 has curated data in GtoImmuPdb

Gene and Protein Information
Species TM AA Chromosomal Location Gene Symbol Gene Name Reference
Human - 404 11q23 CASP1 caspase 1
Mouse - 402 9 A1 Casp1 caspase 1
Rat - 402 8q11 Casp1 caspase 1
Previous and Unofficial Names
ICE | IL-1 β-converting enzyme | p45 | interleukin 1 beta-converting enzyme | IL1BC | caspase 1, apoptosis-related cysteine peptidase
Database Links
Specialist databases
MEROPS C14.001 (Hs)
Other databases
ChEMBL Target
Ensembl Gene
Entrez Gene
Human Protein Atlas
KEGG Enzyme
RefSeq Nucleotide
RefSeq Protein
Enzyme Reaction
EC Number:
Substrates and Reaction Kinetics
Substrate Sp. Property Value Units Standard property Standard value Assay description Assay conditions Comments Reference
Rho GDP dissociation inhibitor beta Hs - -
parkin Hs - -
pro-caspase 4 Hs - -
pro-interleukin-1β Hs - -

Download all structure-activity data for this target as a CSV file

Key to terms and symbols View all chemical structures Click column headers to sort
Ligand Sp. Action Affinity Units Reference
VRT-043198 Hs Inhibition 9.1 pKi 6
pKi 9.1 (Ki 8x10-10 M) Derived from pro-drug belnacasan [6]
pralnacasan Hs Inhibition 9.0 pKi 5
pKi 9.0 (Ki 1x10-9 M) [5]
uracil 20 Hs Inhibition 8.0 pIC50 3
pIC50 8.0 (IC50 9.8x10-9 M) [3]
Description: IC50 in a biochemical assay.
M826 Hs Inhibition 7.3 pIC50 4
pIC50 7.3 (IC50 5x10-8 M) [4]
AS101 Hs Inhibition - - 2
Z-YVAD-FMK Hs Inhibition - - 1


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1. Avivi-Green C, Polak-Charcon S, Madar Z, Schwartz B. (2002) Different molecular events account for butyrate-induced apoptosis in two human colon cancer cell lines. J. Nutr., 132 (7): 1812-8. [PMID:12097652]

2. Brodsky M, Yosef S, Galit R, Albeck M, Longo DL, Albeck A, Sredni B. (2007) The synthetic tellurium compound, AS101, is a novel inhibitor of IL-1beta converting enzyme. J. Interferon Cytokine Res., 27 (6): 453-62. [PMID:17572009]

3. Fournier J-FF, Clary L, Chambon S, Dumais L, Harris CSS, Millois-Barbuis C, Pierre R, Talano S, Thoreau E et al.. (2018) Rational Drug Design of Topically Administered Caspase 1 Inhibitors for the Treatment of Inflammatory Acne. Journal of Medicinal Chemistry, Just Accepted Manuscript.

4. Han Y, Giroux A, Colucci J, Bayly CI, Mckay DJ, Roy S, Xanthoudakis S, Vaillancourt J, Rasper DM, Tam J et al.. (2005) Novel pyrazinone mono-amides as potent and reversible caspase-3 inhibitors. Bioorg. Med. Chem. Lett., 15 (4): 1173-80. [PMID:15686936]

5. Linton SD. (2005) Caspase inhibitors: a pharmaceutical industry perspective. Curr Top Med Chem, 5 (16): 1697-717. [PMID:16375749]

6. Wannamaker W, Davies R, Namchuk M, Pollard J, Ford P, Ku G, Decker C, Charifson P, Weber P, Germann UA et al.. (2007) (S)-1-((S)-2-{[1-(4-amino-3-chloro-phenyl)-methanoyl]-amino}-3,3-dimethyl-butanoyl)-pyrrolidine-2-carboxylic acid ((2R,3S)-2-ethoxy-5-oxo-tetrahydro-furan-3-yl)-amide (VX-765), an orally available selective interleukin (IL)-converting enzyme/caspase-1 inhibitor, exhibits potent anti-inflammatory activities by inhibiting the release of IL-1beta and IL-18. J. Pharmacol. Exp. Ther., 321 (2): 509-16. [PMID:17289835]

How to cite this page

C14: Caspase: Caspase 1. Last modified on 13/04/2018. Accessed on 20/01/2019. IUPHAR/BPS Guide to PHARMACOLOGY,