biohacking$bioLLM CA: TBA

database / hormone

Icatibant

also known as Firazyr

approved hormone cardiovascularimmune sequence not characterised
SOOOOOOOOOOOOONNNNNNNNNNNNNNNNNNNHHHHHHHHHHHHHHHHHHHHHH
92 heavy atoms · 187 bonds · drag to pan, scroll to zoom C59N19O13S1

Skeletal structure drawn from the computed atomic coordinates in PubChem CID 6918173. Carbons are implicit vertices; hydrogens on carbon are suppressed, as in any structural formula. Nothing here is estimated — every atom sits where PubChem placed it.

Research reference only. The observations below are recorded in the cited literature. Nothing here is advice or a recommendation, and no dosing information is published on this site.

Sequence

Primary structure not characterised in the public records this index draws on. Nothing is shown rather than something invented.

A bradykinin B2 antagonist containing five non-proteinogenic residues.

Molecular data

Chemical fields come from the PubChem compound record; computed values are derived from the sequence shown above.
molecular formulaC59H89N19O13S
molecular weight1304.5 Da (PubChem)
computed backbone massnot characterised
lengthnot characterised
net charge (pH 7.4)not characterised
mean hydropathynot characterised
half-lifenot characterised
delivery routesubcutaneous
PubChem CID6918173
PDBnot characterised
UniProt parentnot characterised

Mechanism

Selective bradykinin B2 receptor antagonist.

Reported targets: BDKRB2

Experimental structure

No experimental structure of this peptide is deposited in the PDB. Nothing is rendered here — a predicted fold would not be a structure, and this site does not draw one.

Reported effects

Each row is an outcome described in the literature indexed for this peptide. Reported in the cited work — not a claim, not a recommendation.

Reported observations and the corpus they are drawn from.
reported outcomewhere it appears
hereditary angioedema attack resolution in trialsReal-World Safety and Effectiveness of Icatibant in Patients With Hereditary… The Journal of dermatology 2026

Registered trials

Records from ClinicalTrials.gov. Listed for reference — this project sponsors no trial and is not involved in any of them.
NCTtitlestatusphase
NCT04654351A Study of Icatibant (TAK-667) in Japanese Children and Teenagers With Acute Attacks of HereCOMPLETEDPHASE3
NCT02826356Analysis of the Availability of the Treatments for ACE-I and ARB-induced AngioedemaCOMPLETED
NCT04057131FIRAZYR General Drug Use-Results Survey (Japan)COMPLETED
NCT04978051Investigating the Efficacy and Safety ICATIBANT For The Treatment of Patients With SARS-CoV-COMPLETEDPHASE2
NCT00965120The Effect of Ischaemic-Reperfusion in Man - A Bradykinin Dependent PathwayCOMPLETEDNA

Literature (8)

Real-World Safety and Effectiveness of Icatibant in Patients With Hereditary Angioedema (HAE): Post-Marketing Surveillance in Japan — The Journal of dermatology 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 42630033 · DOI 10.1111/1346-8138.70447

Icatibant for acute hereditary angioedema attacks in pediatric patients: A systematized review — Allergy and asthma proceedings 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 42343494 · DOI 10.2500/aap.2026.47.260042

Overactivated bradykinin-B2 receptor promotes type a aortic dissection by inducing endothelial dysfunction: Therapeutic effect of icatibant — Life sciences 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 42413717 · DOI 10.1016/j.lfs.2026.124572

On-demand treatment of icatibant in a patient of hereditary angioedema with KNG1 mutation — Genes & diseases 2027

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 42656409 · DOI 10.1016/j.gendis.2026.102233

Icatibant — National Institute of Child Health and Human Development, Bethesda (MD) 2006

No information is available on the excretion of icatibant into breastmilk. Because icatibant is a protein molecule with a molecular weight of 1305 Da, the amount in milk is likely to be very low. It is also likely to be partially destroyed in the infant's gastrointestinal tract and absorption by the infant is probably minimal. One patient reportedly used the drug safely during breastfeeding. Waiting 6-12 hours after a dose before breastfeeding should minimize the amount of drug excreted into breastmilk.[1]

open access ↗ · PMID 36940272

Completion of the Icatibant Outcome Survey and What We Learned — Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

open access ↗ · PMID 41808316 · DOI 10.1111/cea.70271

Modest Contribution of Bradykinin to Blood Pressure Reduction by Sacubitril/Valsartan in Chronic Heart Failure — Circulation. Heart failure 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 42028604 · DOI 10.1161/circheartfailure.125.014117

Icatibant Acts as a Balanced Ligand of MRGPRX2 in Human Skin Mast Cells — Biomolecules 2025

MRGPRX2 (Mas-related G protein-coupled receptor member X2) is implicated in mast cell (MC)-driven disorders due to its ability to bind diverse ligands, which may be G-protein-biased or balanced, with the latter activating both G-proteins and the β-arrestin pathway. Icatibant, a peptide drug, produces injection-site reactions in most patients and is used experimentally to probe MRGPRX2 function in skin tests. While reported to be G-protein-biased, it is unknown how skin MCs respond to icatibant, although these are the primary target cells during therapy. We therefore compared responses to icatibant with those induced by the balanced agonist substance P (SP) in skin MCs. Degranulation and desensitization were assessed via β-hexosaminidase release, receptor internalization by flow cytometry, and downstream signaling by immunoblotting. Skin MCs degranulated in response to SP and icatibant, r…

open access ↗ · PMID 41008531 · DOI 10.3390/biom15091224

Related

Glucagon

hormone · 8 citations

Ghrelin

hormone · 8 citations

Oxytocin

hormone · 8 citations

Vasopressin

hormone · 8 citations

Gonadorelin

hormone · 8 citations

Kisspeptin-10

hormone · 8 citations