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Results for "

IRI

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    330
    TargetMol | Inhibitors_Agonists
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    3
    TargetMol | Peptide_Products
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    11
    TargetMol | Inhibitory_Antibodies
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    121
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    14
    TargetMol | Inhibitors_Agonists
SRS16-86
T90731793052-96-6
SRS16-86 is a novel third-generation ferrostatin, is an inhibitor of ferroptosis.
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IRI-426
IRI426, Ac-Arg-Pro-Asp-Val-Phe-NH2
T32192103143-78-8
IRI-426 is a bioactive chemical.
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IRI-514
TP2937147489-65-4
IRI-514 is a synthetic peptide analog of Thymopentin. It plays a role in modulating behavioral and neuroendocrine responses to stress.
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Firibastat
RB-150, RB150, RB 150, QGC-001, QGC001, QGC 001
T28482648927-86-0
Firibastat (RB150) is a glutamyl aminopeptidase antagonist and an orally active brain penetrating prodrug of EC33. It is a first-in-class brain aminopeptidase A (APA) inhibitor with a Ki of 200 nM. Firibastat selectively and specifically inhibits conversion of brain angiotensin-II into angiotensin-III and decreases blood pressure in hypertensive rats[1][2].
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TargetMol | Inhibitor Hot
Flavopiridol
NSC 649890 HCl, L868275, HMR-1275, Alvocidib
T6837146426-40-6
Flavopiridol (Alvocidib) (Alvocidib) competes with ATP to inhibit CDKs including CDK1, CDK2, CDK4 and CDK6 with IC50 of ~ 40 nM. It is 7.5-fold more selective for CDK1, 2, 4, 6 versus CDK7. Flavopiridol is initially found to inhibit EGFR and PKA. Phase 1 2.
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TargetMol | Inhibitor Hot
Fluspirilene
Redeptin, R 6218
T153011841-19-6In house
Fluspirilene (R 6218) is a non-competitive L-type calcium channel antagonist (IC50: 0.03 μM).Fluspirilene is a long-acting antipsychotic compound used in the treatment of schizophrenia.
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8-10weeks
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Sotirimod
S-30594, R850
T16913227318-75-4In house
Sotirimod(R850) is a novel immunomodulator with antitumor and antiviral activity for the study of actinic keratoses.
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6-8 weeks
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Triciribine phosphate
VQD-002, VD 002, TCN-P
T1969961966-08-3In house
Triciribine phosphate (VD 002) is a highly selective AKT inhibitor that induces cell cycle arrest and cysteinyl asparagin-dependent apoptosis, inhibits neovascularization, and can be used in the study of leukemia.
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6-8 weeks
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Piritrexim
BW 301U
T2464472732-56-0In house
Piritrexim (BW 301U) is an orally available fat-soluble dihydrofolate reductase inhibitor with pulmonary toxicity used in the study of uroepithelial carcinoma and metastatic breast cancer.
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6-8weeks
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Levovirin
ICN-17261, ICN 17261, ICN17261, L-Ribavirin
T25702206269-27-4In house
Levovirin (L-Ribavirin), the L-enantiomer of ribavirin, is a guanosine nucleoside analog with immunomodulatory activity and is used in the study of hepatitis C virus infection.
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Efletirizine
UCB-28754, UCB28754, UCB 28754
T27244150756-35-7In house
Efletirizine (UCB-28754) is a histamine receptor antagonist with inhibitory effects on the enzyme 5-lipoxygenase (5-LO), and is useful in the topical treatment of allergic diseases.
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6-8 weeks
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TargetMol | Inhibitor Sale
Niridazole
BA32644, BA-32644, Ambilhar, BA 32644
T2817461-57-4In house
Niridazole (Ambilhar) is an antiparasitic compound belonging to nitroimidazoles. Niridazole is primarily used to treat schistosomiasis, which kills the parasite by interfering with its metabolism. Niridazole rapidly concentrates in the parasite, inhibits egg and sperm production, and inhibits phosphofructokinase activity.
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6-8weeks
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Tirilazad mesylate
U-74006 mesylate, U74006 mesylate, U 74006 mesylate, U 74006F mesylate, U-74006F mesylate, U74006F mesylate
T28978110101-67-2In house
Tirilazad mesylate (U 74006F) is a non-glucocorticoid, lipid peroxidation inhibitor with antiviral and neuroprotective activities. It confines intracellular intramembranous foci, attenuates spinal cord injuries induced by trauma, stroke, and ischemia reperfusion injuries, inhibits toxins in dogs, and is used in the study of neurological disorders.
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7-10 days
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Epetirimod
S-30563, S30563, S 30563
T31648227318-71-0In house
Epetirimod (S-30563) is a small molecule immunomodulator with antitumor and anti-infective activity for the study of papillomavirus infections.
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6-8weeks
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Fosdevirine
GSK-2248761A, IDX 899, GSK 2248761A, GSK 2248761, GSK-2248761, IDX-12899, GSK2248761, FDV, GSK2248761A
T318601018450-26-4In house
Fosdevirine (GSK2248761) is a selective and potent non-nucleoside reverse transcriptase (NNRTI) inhibitor with anti-HIV activity for the study of neurological related disorders such as late-onset epilepsy.
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6-8weeks
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(Iso)-Fosdevirine
(Iso)-Fosdevirine(Iso-1018450-26-4), (Iso)-GSK2248761
T31860L2869918-45-4In house
(Iso)-Fosdevirine ( (Iso)-GSK2248761) is a selective and potent non-nucleoside reverse transcriptase (NNRTI) inhibitor with anti-HIV activity for the study of neurological disorders such as late-onset epilepsy.
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Giripladib
PLA 695, PLA-695, PLA695
T31929865200-20-0In house
Giripladib (PLA695)(PLX-695) is a cPLA2-specific inhibitor that inhibits the radiation-induced increase of phosphorylated ERK and phosphorylated Akt in endothelial cells.
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6-8 weeks
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Miricorilant
CORT-118335, CORT118335, CORT 118335
T333931400902-13-7In house
Miricorilant (CORT 118335) is a selective glucocorticoid receptor modulator for the study of digestive and metabolic disorders.
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Biricodar dicitrate
VX 710-3
T67790174254-13-8In house
Biricodar dicitrate (VX-710) is a potent MDR inhibitor with no anticancer activity and can be used to study prostate cancer.
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6-8weeks
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Girisopam
T6808182230-53-3In house
Girisopam is a novel selective benzodiazepine analog for the 2,3-benzodiazepine binding site, an atypical psychoanalytic with anxiolytic effects.
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TargetMol | Inhibitor Sale
Girinimbine
Girinimbin
TN609723095-44-5In house
Girinimbine (Girinimbin) is a carbazole alkaloid isolated from the plants M. koenigii, M. koenigii, and Murraya koenigii. Girinimbine exhibits a wide range of biological effects, including apoptosis, antitrypanosomal, antiplatelet, antimicrobial, anti-inflammatory, antioxidant, and antitumor activities.
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Aspirin
ASA, Acetylsalicylic Acid, Acetylsalicylate
T000550-78-2
Aspirin (Acetylsalicylic Acid) is a COX inhibitor that inhibits COX1 and COX2 (IC50=5 210 μg mL) with selective, irreversible, and oral activity. Aspirin is also a histone deacetylase inhibitor that up-regulates the cell cycle blocking protein, p21. Aspirin has a variety of activities. Aspirin has anti-inflammatory, antipyretic and analgesic, and antiplatelet aggregation activities.
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Cetirizine dihydrochloride
UCB P071, P071, Cetirizine DiHCl
T008983881-52-1
Cetirizine dihydrochloride (UCB P071) is an effective second-generation histamine H1 antagonist that is potent in the therapy of allergic rhinitis, confirmed urticaria, and pollen-induced asthma. Unlike other conventional antihistamines, it does not cause side effects of drowsiness or anticholinergic.
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Glimepiride
HOE-490, Glimperide
T012793479-97-1
Glimepiride (HOE-490) is a long-acting, third-generation sulfonylurea with hypoglycemic activity.
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