PHENYLEPHRINE HCL

Phenylephrine HCl is an alpha1 agonist causing vasoconstriction, used as a decongestant and to increase blood pressure during anesthesia. Side effects include hypertension, headache, anxiety, reflex bradycardia, and insomnia; excessive use can cause rebound congestion. Only GMP materials will be supplied, logistics all according to GDP.

SKU: c1e5ca5424bf Category: Tag:

Product Description


Mechanism of Action

PHENYLEPHRINE HCL demonstrates a broad, multilayer biochemical activity profile affecting enzymedriven catalytic pathways, receptorregulated signalling systems, mitochondrial bioenergetics, redoxstate equilibrium, ionchannel behaviour, cytoskeletal integrity and transcriptionfactor regulatory networks. Its structural features indicate potential interactions with catalytic residues, allosteric protein domains, membranebound receptors and intracellular signalling intermediates, enabling influence over phosphorylation kinetics, Ca²⁺/cAMP/IP/DAGmediated secondmessenger systems, ATP turnover, ROS buffering and mitochondrial respiratorychain performance.

Depending on concentration and biological conditions, PHENYLEPHRINE HCL may modulate metabolic flux distribution, alter mitochondrial membrane potential, influence chromatin accessibility, impact vesicular trafficking dynamics and reshape geneexpression patterns relevant to survival, inflammation, apoptosis, autophagy, metabolic adaptation and redoxstress response.

Benefits and Advantages

This compound is widely used across advanced biochemical, pharmacological and mechanistic research domains, including:

  • Receptorligand interaction studies and affinitymapping
  • Enzymekinetic pathway deconstruction and catalyticdomain profiling
  • Mitochondrialfunction analysis and ATPflux/oxidativestress modelling
  • Multiomics integration (transcriptomics, metabolomics, proteomics, phosphoproteomics)
  • Cytoskeletalstructure and membranedynamics research
  • Autophagy, apoptosis, necroptosis and ferroptosis signalling investigations
  • SAR (structureactivity relationship) profiling and compoundoptimisation workflows
  • Pharmacodynamic modelling, thresholdactivation mapping and doseresponse scaling

Side Effects and Risks

Laboratoryobserved or predicted risks include:

  • Oxidative imbalance and excessive ROS accumulation
  • Mitochondrial overload or respiratorychain suppression
  • Dysregulation of Na⁺/K⁺/Ca²⁺ ionchannel homeostasis
  • Unintended receptor crosstalk or inhibitory interference
  • Cytoskeletal destabilisation and membrane-integrity disruption
  • Dosedependent cytotoxicity with apoptosis/autophagy activation
  • Transcriptional instability or epigenetic disturbance
  • Inflammatory signalling activation via NF-κB, MAPK or JNK pathways

Use strictly within controlled laboratory environments under appropriate biosafety protocols.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C9H13NO2·HCl

Molecular Weight

203.66 g/mol

CAS Number

61-76-7

Storage Condition

Store below 40 °C (104 °F), preferably between 15 and 30 °C (59 and 86 °F), unless otherwise specified by manufacturer. Store in a tight, light-resistant container if not more than 15 mL size. Protect from freezing.

Solubility

greater than or equal to 100 mg/mL at 70 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

PHENYLEPHRINE HYDROCHLORIDE; 61-76-7; Phenylephrine HCl; Biomydrin; Mydfrin

IUPAC/Chemical Name

3-[(1R)-1-hydroxy-2-(methylamino)ethyl]phenol;hydrochloride

InChl Key

OCYSGIYOVXAGKQ-FVGYRXGTSA-N

InChl Code

InChI=1S/C9H13NO2.ClH/c1-10-6-9(12)7-3-2-4-8(11)5-7;/h2-5,9-12H,6H2,1H3;1H/t9-;/m0./s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/5284443;

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