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Results for "

intravenous

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    70
    TargetMol | Inhibitors_Agonists
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    2
    TargetMol | Peptide_Products
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    TargetMol | Inhibitors_Agonists
Copanlisib
BAY 80-6946
T63221032568-63-0
Copanlisib (BAY 80-6946) is a phosphoinositide 3-kinase (PI3K) inhibitor with potential antineoplastic activity. By inhibiting the PI3K signaling pathway, Copanlisib may impede tumor cell growth and survival in certain tumor populations. Dysregulated PI3K signaling, often linked to tumorigenesis, may also contribute to tumor resistance to various antineoplastic agents.
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Gadopentetic acid
Gd-DTPA, gadolinium complex
T1933280529-93-7
Gadopentetic acid (gadolinium complex) (Gd-DTPA) is an paramagnetic contrast agent commonly implemented by a bolus intravenous injection (i.v.) in Dynamic contrast-enhanced MRI (DCE-MRI) studies.
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TargetMol | Inhibitor Hot
Oxaquin
MCB-3837, DNV3837
T12337790704-50-6In house
Oxaquin is an effective, water-soluble, injectable prodrug that is rapidly converted to the active substance MCB3681 after intravenous administration in the body. Oxaquin is active against Gram-positive bacteria, but has no antibacterial effect on its own.
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3-6 months
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Propanidid
Sombrevin, FBA 1420, Fabontal, Fabantol, Epontol
T341461421-14-3In house
Propanidid (Sombrevin) is a gamma-aminobutyric acid type A receptor (GABAA) agonist and a fast-acting intravenous anesthetic that lowers arterial blood pressure.
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7-10 days
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GAL-021
GAL 021
T35571380341-99-0In house
GAL-021 an intravenous BKCa-channel blocker.
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(Rac)-Upacicalcet
T612322649575-19-7In house
(Rac)-Upacicalcet is a racemate of Upacicalcet, which serves as an intravenous calcimimetic agent. Upacicalcet acts by directly targeting calcium-sensing receptors on parathyroid cell membranes, effectively suppressing the release of excessive parathyroid hormone (PTH) and reducing blood PTH levels. This compound holds the potential for researching secondary hyperparathyroidism (SHPT) [1].
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6-8weeks
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Fosphenytoin
T6135493390-81-9In house
Fosphenytoin is a phosphate prodrug that can be used as an alternative to intravenous phenytoin for the acute intervention of seizures.Fosphenytoin is hydrolyzed to anticonvulsant phenytoin when administered parenterally.Fosphenytoin can be used in a variety of delivery modes such as intravenous and intraperitoneal.Fosphenytoin can be used in a variety of delivery modes such as intravenous and intraperitoneal.
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6-8 weeks
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Iodipamide
Iodipamic acid, Adipiodone
T0271606-17-7
Iodipamide (Iodipamic acid) is a water-soluble radiographic contrast media for intravenous cholangiography and cholecystography.
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Miconazole
R18134
T034422916-47-8
Miconazole (R18134) is an imidazole antifungal agent used both topically and via intravenous infusion.
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Cisatracurium besylate
51W89
T145996946-42-8
Cisatracurium besylate (51W89) is a nondepolarizing skeletal muscle relaxant intended for intravenous administration.
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Fosaprepitant dimeglumine
MK-0517, L785298, Fosaprepitant dimeglumine salt
T1790265121-04-8
Fosaprepitant dimeglumine (MK-0517) is the dimeglumine salt form of fosaprepitant, a water-soluble, N-phosphorylated prodrug of aprepitant with antiemetic activity. Upon intravenous administration and rapid conversion to aprepitant, this agent selectively binds to human substance P neurokinin 1 (NK1) receptors in the central nervous system (CNS), inhibiting receptor binding of endogenous substance P and preventing substance P-induced emesis.
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Tempone
4-Oxo-tempo
T365062896-70-0
Tempone is an aminooxyalkane that acts as a free radical scavenger and reacts with reactive oxygen species (ROS). Intravenous Tempone reduces mean arterial pressure in spontaneously hypertensive rats.
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TargetMol | Inhibitor Sale
Methyl eugenol
O-methyleugenol, eugenyl methyl ether, Eugenol Methyl ether, 4-allylveratrole
T3S225993-15-2
1. Methyl eugenol (4-allylveratrole) is a natural constituent of the essential oils of a number of plants widely used in foodstuffs as flavouring agents, in view of the carcinogenic potential of ME, the need to check its presence in food products with effective analytical methods. 2. Methyleugenol has insecticidal properties. 3. Methyleugenol can inhibit the production of nitric oxide and decreased the protein expression of inducible nitric oxide synthase, it down-regulates the production of pro-inflammatory cytokines in the ischemic brain as well as in immunostimulated mixed glial cells; indicates that methyleugenol could be useful for the treatment of ischemia inflammation-related diseases. 4. Methyleugenol has cytotoxicity and genotoxicity. 5. Intravenous (i.v.) treatment with methyleugenol (ME) in either anesthetized or conscious rats elicits hypotension, an effect that seems related to an active vascular relaxation rather than withdrawal of sympathetic tone. 6. Methyleugenol has antinociceptive effect on the second phase of formalin-induced pain, may be due to the inhibition of N-methyl-d-aspartic acid (NMDA) receptor-mediated hyperalgesia via GABA(A) receptors. 7. Methyleugenol has elaxant and antispasmodic actions on guinea-pig isolated ileum.
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Iron sucrose
Iron saccharate, Sucroferric oxyhydroxide
T81328047-67-4
Iron sucrose (Sucroferric oxyhydroxide) is treatment of iron deficiency anemia.
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Copanlisib dihydrochloride
BAY 80-6946 dihydrochloride
T149981402152-13-9
Copanlisib dihydrochloride (BAY 80-6946 dihydrochloride) is an ATP-competitive pan-class I PI3K inhibitor, with IC50 values of 0.5 nM for PI3Kα, 0.7 nM for PI3Kδ, 3.7 nM for PI3Kβ, and 6.4 nM for PI3Kγ. It exhibits superior antitumor activity and demonstrates more than 2,000-fold selectivity against other lipid and protein kinases, except for mTOR.
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Lanatoside C
Isolanid, Ceglunate, Cedilanid
T167017575-22-3
Lanatoside C (Ceglunate) is a cardiac glycoside, a type of drug that can be used in the treatment of congestive heart failure and cardiac arrhythmia (irregular heartbeat). Lanatoside C can be used orally or by the intravenous route.
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Cangrelor free acid
T70335163706-06-7
Cangrelor is a P2Y12 inhibitor, and was approved in June 2015 as an antiplatelet drug for intravenous application. Cangrelor is a high-affinity, reversible inhibitor of P2Y12 receptors that causes almost complete inhibition of ADP-induced platelet aggregate. It is a modified ATP derivative stable to enzymatic degradation. It does not require metabolic conversion to an active metabolite. This allows cangrelor's immediate effect after infusion, and the therapeutic effects can be maintained with continuous infusion.
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1-2 weeks
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1V209
TLR7 agonist T7
T83161062444-54-5
1V209 (TLR7 agonist T7) is a Toll-like receptor 7 (TLR7) agonist known for its anti-tumor properties.
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Artemitin
Artemetin, Artemisetin, Erianthin
TCS1704479-90-3
1. Artemitin (Erianthin) has anti-inflammatory activity. 2. Artemitin (Erianthin) protects endothelial function by acting as antioxidant and antiapoptotic agent and through the activation of ERK1 2 and Akt. 3. Intravenous injection of Artemitin (Erianthin)(.75 mg kg) significantly reduces the hypertensive response to angiotensin I while increases the average length of bradykinin-induced hypotension.
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Tiprenolol hydrochloride
DU 21445 hydrochloride
T20176013379-87-8
Tiprenolol hydrochloride is a β-adrenoceptor (β-adrenoceptor) antagonist. This compound is effective in eliminating ventricular arrhythmias in dogs caused by intravenous administration of adrenaline, following inhalation of halothane.
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10-14 weeks
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Lipid 29d
T2018872921586-67-4
Lipid 29 is an unsaturated, ionizable cationic lipid that facilitates the formation of lipid nanoparticles (LNP) used for intrabody mRNA delivery. When integrated into LNPs encapsulating luciferase reporter gene mRNA, intravenous injection of these LNPs induces bioluminescence in the lungs and spleen of mice.
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Benapenem
T2019931312953-83-5
Benapenem is a carbapenem (β-lactam) compound known for its broad-spectrum antibacterial activity. It is currently under clinical evaluation as an intravenous treatment option for urinary tract infections.
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Venelbin
T20296776515-02-1
Venelbin, a compound administered after intravenous sclerosis, contains dihydroergotamine and troxerutin.
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BF-170
T20548022191-97-5
BF-170 is a selective tau fiber-binding agent with an EC50 of 221 nM. It demonstrates excellent blood-brain barrier penetration, reaching a concentration of 9.1% ID g in brain tissue 2 minutes after intravenous injection in mice (with a clearance rate of 0.25% ID g at 30 minutes). BF-170 can serve as a probe for imaging tau protein pathology in Alzheimer's disease (AD). It plays a significant role in early-stage Alzheimer's disease studies and holds promise for imaging research in tau-related neurodegenerative diseases.
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10-14 weeks
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