Table 1 Comprehensive in vitro pharmacology profile of TRP601

From: Targeting neonatal ischemic brain injury with a pentapeptide-based irreversible caspase inhibitor

Non-peptide receptors

Peptide receptors

Nuclear receptors

Adenosine

Angiotensin-II

Glucocorticoid

Adrenergic

Bombesin

Estrogen alpha

Cannabinoid

Calcitonin gene-related peptide

Androgen

Dopamine

Chemokine

 

GABA

Cholecystokinin

Ion channels

Glutamate

Complement 5a

Ca2+ channels

Glycine

Endothelin

K+ channels

Histamine

Galanin

Na+ channel

Imidazole

Glucagon

 

Leukotriene

Growth hormone secretagogue

Enzymes

Melatonin

Melanin-concentrating hormone

 Kinases

Muscarinic

Motilin

 Phosphatases

Nicotinic

Neurokinin

 Serine proteases

Purinergic

Neuropeptide Y

 Cysteine proteases

Serotonin

Neurotensin

 Aspartate proteases

Sigma

Opioid and opioid-like

 Arachidonic acid metabolism

 

Somatostatin

 Prostaglandin metabolism

Amine transporters

Thyroid hormone

 Monoamine synthesis and metabolism

 Choline

Urotensin-II

 Neurotransmitter synthesis and metab.

 Dopamine

Vasoactive intestinal peptide

 Nitric oxide synthesis

 GABA

Rolipram

 Second messenger systems

 Norepinephrine

Vasopressin

 ATPases

 Seretonin

 

 Lipid synthesis

  

 Metalloproteases

  

 Miscellaneous enzymes

  1. TRP601 (10 μM) did not significantly modify the activity of 56 enzymes and did not impair or increase the binding of specific ligands to their receptors (110 receptors, channels, or transporters tested). Synthetic list of enzymes, peptide and non-peptide receptors, nuclear receptors, ion channels, or amine transporters, challenged with TRP601 (see details in Supplementary Table S3)