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Results for "

postoperative

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    30
    TargetMol | Inhibitors_Agonists
  • Peptide Products
    1
    TargetMol | Peptide_Products
  • Recombinant Protein
    1
    TargetMol | Recombinant_Protein
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    TargetMol | Isotope_Products
Doxpicomine
T6805762904-71-6In house
Doxpicomine has analgesic activity and can be used to treat postoperative pain.
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Amantadine hydrochloride
Symmetrel, CI-719, Amantadine HCl, 1-Adamantylamine hydrochloride, 1-Adamantanamine hydrochloride, 1-adamantanamine HCl
T1406665-66-7
Amantadine hydrochloride (CI-719) is an antiviral that is used in the prophylactic or symptomatic treatment of influenza A and Parkinson disease.
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Parecoxib
SC 69124, Vorth-P, Valus-P
T1780198470-84-7
Parecoxib (SC 69124) is an effective and selective COX-2 inhibitor.
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Ketorolac
Toradol, Sprix, Macril, Acuvail, Acular
T2141274103-06-3
Ketorolac (Acuvail) is a non-steroidal anti-inflammatory drug (NSAID) in the family of heterocyclic acetic acid derivatives. It acts by inhibiting the bodily synthesis of prostaglandins.
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Bethanechol chloride
(±)-Bethanechol, Urecholine, Myocholine, Carbamyl-β-methylcholine chloride
T3126590-63-6
Bethanechol chloride (Carbamyl-β-methylcholine chloride) is a slowly hydrolyzing muscarinic agonist with no nicotinic effects. It is used to increase smooth muscle tone in the GI tract following abdominal surgery or to treat urinary retention without obstruction. Possible side effects include hypotension, heart rate changes, and bronchial spasm.
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Ozagrel
OKY-046, Domenan
T623682571-53-7
Ozagrel (Domenan) is a selective thromboxane A(2) (TXA(2)) synthetase inhibitor with IC50 of 11 nM for rabbit platelet, used for the improvement of postoperative cerebrovascular contraction and accompanying cerebral ischaemia.
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Ozagrel hydrochloride
Ozagrel HCl, OKY-046 HCl
T662578712-43-3
Ozagrel hydrochloride (OKY-046 HCl) is a selective thromboxane A(2) synthetase inhibitor used for the improvement of postoperative cerebrovascular contraction and accompanying cerebral ischaemia.
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Centhaquin
PMZ-2010, Centhaquine
T815757961-90-7
Centhaquin (Centhaquine)e is an adrenergic receptor potentially for the treatment of postoperative pain and for the resuscitation of hypovolemic shock
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TargetMol | Inhibitor Sale
Alvimopan
T1242156053-89-3
Alvimopan (LY 246736) is a synthetic trans-3, 4-dimethyl-4-(3-hydroxyphenyl) piperidine with peripherally selective opioid mu receptor antagonist activity. Alvimopan is a selective and competitive antagonist at mu-opioid receptors, found in myenteric and submucosal neurons and the immune cells of the lamina propria in the human gut. Upon administration, this agent binds to mu-opioid receptors in the gut, thereby reversing opioid-related disturbances in gut motility. Alvimopan is approximately three to nine times more potent than naloxone.
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(R,R)-Palonosetron Hydrochloride
T13437135729-75-8
(R,R)-Palonosetron Hydrochloride, the active enantiomer of Palonosetron, is a selective 5-HT3 receptor antagonist used primarily for the prevention of chemotherapy-induced nausea and vomiting (CINV) and postoperative nausea and vomiting (PONV).
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3-6 months
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Opiranserin
T163991441000-45-8
Opiranserin is a development as an injectable agent for the treatment of postoperative pain. Opiranserin is a non-opioid and non-NSAID analgesic candidate and is a dual antagonist of glycine transporter type 2 (GlyT2) and serotonin receptor 2A (5HT2A) (IC50s: 0.86 and 1.3 μM, respectively). Opiranserin displays antagonistic activity on rP2X3 (IC50=0.87 μM).
  • Inquiry Price
1-2 weeks
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Parecoxib sodium
SC 69124A,SC-69124A,SC69124A,Dynastat
T1780L198470-85-8
Parecoxib is a cyclooxygenase-2 inhibitor used for the short-term treatment of postoperative pain in adults. Parecoxib is a water-soluble and injectable prodrug of valdecoxib. Parecoxib is a COX2 selective inhibitor in the same category as celecoxib and r
  • Inquiry Price
7-10 days
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Suxethonium bromide
MB 2210, M-115, M 115, IS-362, IS 362, BREVIDIL E
T202123111-00-2
Suxethonium is a depolarizing muscle relaxant known for its lower incidence of postoperative muscle pain.
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NeoSTX
neosaxitoxina, Neosaxitoxin solution, Neosaxitoxin
T20288464296-20-4
NeoSTX (Neosaxitoxin) is a specific sodium channel blocker that targets site 1. It works synergistically with local anesthetics to provide surgical anesthesia through peripheral nerve block or local infiltration and significantly prolongs postoperative analgesia duration.
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Casopitant
GW679769
T203625414910-27-3
Casopitant (GW679769) is an orally active neurokinin-1 (NK1) receptor antagonist, researched for its potential use in managing chemotherapy-induced nausea and vomiting (CINV) and postoperative nausea and vomiting (PONV).
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Alvimopan dihydrate (LY246736 dihydrate)
T22238170098-38-1
Alvimopan dihydrate (ADL 8-2698 dihydrate) is a potent, selective, orally active, and reversible μ-opioid receptor antagonist with an IC50 of 1.7 nM. Highly selective for the μ-opioid receptor (Ki = 0.47 nM) over κ- and δ-opioid receptors (Kis = 100 and 12 nM, respectively), Alvimopan dihydrate can be used for research on postoperative ileus [1] [2] [3].
  • Inquiry Price
7-10 days
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CR-665 Acetate
FE200665,CR-665,JNJ-38488502,CR665,FE-200665,JNJ38488502
T27079958873-83-1
CR-665, a kappa-opioid agonist, is used potentially for the treatment of postoperative pain.
  • Inquiry Price
6-8 weeks
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Felbinac Trometamol
L141, L-141, L 141
T31759935886-64-9
Felbinac Trometamol is an intravenous preparation used to treat severe postoperative pain.
  • Inquiry Price
1-2 weeks
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Propacetamol
T6043566532-85-2
Propacetamol is an analgesic agent and a prodrug that is metabolized to paracetamol. It can be used for postoperative pain, acute trauma, and gastrointestinal disorders[1].
    6-8 weeks
    Inquiry
    Ketorolac hemicalcium
    T60496167105-81-9
    Ketorolac (RS37619) hemicalcium is a nonselective COX inhibitor with IC50 values of 20 nM for COX-1 and 120 nM for COX-2. This non-steroidal anti-inflammatory drug (NSAID) is used as a 0.5% ophthalmic solution for researching allergic conjunctivitis, cystoid macular edema, intraoperative miosis, and postoperative ocular inflammation and pain. Additionally, it is a DDX3 inhibitor applicable in cancer research [1] [4].
    • Inquiry Price
    1-2 weeks
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    Piroxicam betadex
    T6821196684-40-1
    Piroxicam betadex is a nonsteroidal anti-inflammatory drug. The mechanism of action of piroxicam is as a cyclooxygenase Inhibitor. It is well established in treating rheumatoid arthritis and osteoarthritis and used for musculoskeletal disorders, dysmenorrhea, and postoperative pain. It is used to reduce pain, swelling, and joint stiffness from arthritis. Reducing these symptoms helps you do more of your normal daily activities.
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    6-8 weeks
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    Piroxicam olamine
    T6856385056-47-9
    Piroxicam olamine is a cyclooxygenase inhibiting, non-steroidal anti-inflammatory agent (NSAID) that is well established in treating rheumatoid arthritis and osteoarthritis and used for musculoskeletal disorders, dysmenorrhea, and postoperative pain. Its long half-life enables it to be administered once daily.
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    1-2 weeks
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    Amantadine
    1-Aminoadamantane, 1-Adamantylamine, 1-Adamantanamine
    T7060768-94-5
    Amantadine (1-Aminoadamantane) is an antiviral, is a weak antagonist of the NMDA-type glutamate receptor, increases dopamine release, and blocks dopamine reuptake.
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    Lornoxicam-d4
    T712121216527-48-8
    Lornoxicam-d4 is intended for use as an internal standard for the quantification of lornoxicam by GC- or LC-MS. Lornoxicam is a COX inhibitor and non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory and analgesic properties. It inhibits production of thromboxane B2 from arachidonic acid in HEL human erythroleukemic cells, which endogenously express COX-1, as well as inhibits LPS-induced formation of prostaglandin F1α from arachidonic acid in Mono-Mac-6 cells, which endogenously express COX-2. Lornoxicam reduces LPS-induced production of nitric oxide and IL-6 in cell-based assays with IC50 values of 65 and 54 µM, respectively. It reduces carrageenan-induced paw edema in rats when administered intravenously at doses ranging from 0.1 to 9 mg kg. Formulations containing lornoxicam have been used in the management of postoperative pain.
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    6-8 weeks
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