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 About 30 results found for searched term "RET" (0.011 seconds)

Cat.No.  Name Target
M1758 Foretinib c-Met
XL880, GSK1363089
Foretinib (XL880, GSK1363089) is a multi-targeted inhibitor of c-Met and vascular endothelial growth factor receptor 2 (VEGFR2) with IC50 value of 0.4 nM for c-MET.
M1797 Retigabine Potassium Channel
Ezogabine; D2312; D-23129
Retigabine is a KCNQ/Kv7 potassium channel activator which functions by enhancing potassium currents via stabilizing the open conformation of the Kv7.2-7.3 channels.
M1961 Acitretin (Ro 10-1670) RAR/RXR
Etretin; Ro 10-1670
Acitretin (Ro 10-1670) is a second-generation retinoid.
M2163 PA-824 Anti-infection
Pretomanid; (S)-PA 824
PA-824 is a novel, orally active nitroimidazole derivative with antimycobacterial activity for use in tuberculosis-related studies.
M2242 Altretamine DNA Alkylator/Crosslinker
Hexalen
Altretamine is an antitumor agent which also acts as a chemosterilant for male houseflies and other insects.
M2274 Fosbretabulin disodium Microtubule
Combretastatin A-4 phosphate, CA4P
Fosbretabulin disodium (Combretastatin A-4 phosphate) is a microtubule-targeting agent that binds β-tubulin with Kd of 0.4 μM.
M2777 IPI-504 hydrochloride HSP
Retaspimycin hydrochloride; IPI-504 hcl
IPI-504 (Retaspimycin) hydrochloride is a potent inhibitor of HSP90 with EC50 of 63 nM.
M2832 Mechlorethamine hydrochloride Others
Mechlorethamine is the prototype of alkylating agents, it works by binding to DNA, crosslinking two strands and preventing cell duplication.
M2887 Norethindrone Progesterone Receptor
Norethisterone
Norethindrone is a synthetic progestin, which mimic the actions of the endogenous ovarian hormone progesterone.
M2974 Retapamulin Antibiotic
SB-275833
Retapamulin (SB-275833) is a topical antibiotic, which binds to both E. coli and S. aureus ribosomes with similar potencies with Kd of 3 nM.
M3150 Fenretinide RAR/RXR
4-HPR
Fenretinide (4-HPR) is a synthetic retinoid deriverative. Fenretinide is shown to exhibit binding to the retinoic acid receptors (RAR) at concentrations necessary to induce cell death.
M3683 Retaspimycin HSP
IPI-504
Retaspimycin is a novel, water-soluble, potent inhibitor of heat-shock protein 90 (Hsp90).
M3901 Combretastatin A4 Microtubule
CRC 87-09, NSC 817373, CA-4
Combretastatin A4 (CA-4), which is a natural stilbene isolated from Combretum caffrum, is a microtubule-destabilizing agent that binds to the colchicine domain on β-tubulin and exhibits a lower toxicity profile than paclitaxel or the Vinca alkaloids.
M3902 Quercetin (>99%) Senolytics
Meletin, Sophoretin
Quercetin is a PI3K inhibitor with IC50 of 2.4-5.4 μM that has been shown to cause potent reversible inhibition of fatty-acid synthase.
M1556 Hesperetin p38 MAPK
Hesperitin
Hesperetin is a potent and broad-spectrum inhibitor against human UGT activity.
M4553 Tangeretin Notch
Tangeritin; NSC53909; NSC618905; Ponkanetin
Tangeretin is a flavonoid from citrus fruit peels, and is also selected as a Notch-1 inhibitor, which plays an important role in anti-inflammatory responses and neuroprotective effects in several disease models.
M4571 Neohesperidin Others
Hesperetin 7-O-neohesperidoside
Neohesperidin is an antioxidant agent with an IC50 of 22.31 μg/ml in the 1,1-diphenyl-2-picryldydrazyl (DPPH) radical-scavenging assay.
M4607 Phloretin SGLT
NSC 407292; RJC 02792
Phloretin (NSC 407292; RJC 02792) is a specific, competitive and orally active inhibitor of sodium/glucose cotransporters in the intestine (SGLT1) and kidney (SGLT2).
M5299 Olumacostat glasaretil Acetyl-CoA Carboxylase
Olumacostat glasaretil is a small molecule inhibitor of acetyl coenzyme A carboxylase (ACC).
M5482 CB1954 Others
Tretazicar
CB1954(Tretazicar) is a anticancer prodrug that is converted in the presence of the enzyme NQO2 and co-substrate caricotamide ( EP-0152R) (EP) into a potent cytotoxic bifunctional alkylating agent. It can be activated by NAD(P)H quinone oxidoreductase 2.
M5636 Etretinate Apoptosis
Tegison, Ethyl etrinoate, Retinoid, Etretinato
Etretinate is an orally available aromatic retinoid that has been shown to be effective in studies of cow skin and other skin syndromes. It can activate retinoid receptor, induce cell differentiation, inhibit cell proliferation and inhibit tissue infiltration.
M5689 Hesperidin Apoptosis
Hesperetin 7-rutinoside
Hesperidin (HP) is a bioflavonoid that plays a role in plant defense and is abundant in citrus species, such as grapefruit, lemon and orange. Hesperidin is used effectively as a supplemental agent in complementary therapy protocols.
M5715 Isotretinoin Others
13-cis-Retinoic acid
Isotretinoin(13-cis-Retinoic acid) is a medication used for the treatment of severe acne. It was first developed to be used as a chemotherapy medication for the treatment of brain cancer, pancreatic cancer and more.*The compound is unstable in solutions, freshly prepared is recommended
M5806 Nandrolone decanoate Androgen Receptor
Deca Durabolin, 19-Nortestosterone decanoate, Retabolil
Nandrolone Decanoate is a mild form of an anabolic steroid.
M5927 Retinoic acid PPAR
ATRA; Tretinoin; Vitamin A acid; all-trans-Retinoic acid
Retinoic acid is A metabolite of vitamin A and plays an important role in cell growth, differentiation and organogenesis. Retinoic acid is a natural agonist of RAR nuclear receptors with an IC50 of 14 nM for RARα/β/γ. The Kd value of Retinoic acid combined with PPARβ/δ is 17 nM. Retinoic acid inhibits the transcription factor Nrf2 by activating Retinoic acid receptors.
M6045 Urethane Animal experimental anesthetics
Carbamic acid ethyl ester, Ethyl carbamate, Ethylurethane
Urethane is a kind of antineoplastic agent that is also used as a veterinary anesthetic. It is a intermediate in organic synthesis.
M6530 Bretazenil Others
Bretazenil is a benzodiazepine partial agonist.
M7523 Potassium acetate Metabolite/Endogenous Metabolite
Diuretic salt, Potassium ethanoate
Potassium acetate is the potassium salt of acetic acid, which is a synthetic carboxylic acid with antibacterial and antifungal properties.
M7964 Nordihydroguaiaretic acid Lipoxygenase
NDGA
Lipoxygenase inhibitor; polyphenol-bearing o-dihydroxy (catechol) structure.
M8438 Retro-2 Anti-infection
Retro-2 is a non-toxic inhibitor of the endosome-to-Golgi retrograde transport that selectively protect cells from ricin, cholera toxin, and Shiga-like toxins, without affecting compartment morphology, endogenous retrograde cargos, or other trafficking steps.



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