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M2206 TH-302 (Evofosfamide) TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM.
M6098 Baicalein Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM.
M9325 EGTA EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages.
M9330 Brij-35 Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability.
M6154 2-PMPA tetrasodium 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM.
M2250 Pamidronate disodium Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis.
M9916 DPPH DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants.
M9194 Insulin (human) Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets.
M3409 Formestane Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM.
M9665 N-(2-amino-2-oxoethyl)acrylamide N-(2-Amino-2-oxoethyl)acrylamide
M54778 Methylarbutin Methylarbutin (ß-PMP-Glc;4-Methoxyphenyl β-D-Glucopyranoside) is an ice recrystallization inhibitor (IRI).
M54641 Murrayafoline A Murrayafoline A is a carbazole alkaloid that enhances calcium inward flow through L-type calcium channels.Murrayafoline A can be used for related research in the life sciences.
M54639 Shizukaol A Shizukaol A is a sesquiterpene dimerizable from Chloranthus japonicas.
M54611 Hynic-TOC Hynic-TOC is a ligand for making 99mTc-Hynic-TOC as an imaging agent in the diagnostic of neuroendocrine tumor.
M54562 FR054 FR054 is a hexosamine biosynthesis pathway enzyme PGM3 inhibitor with anticancer activity and can be used in studies related to breast cancer.
M54560 Benproperine phosphate Benproperine phosphate is an orally active, potent inhibitor of actin-associated protein 2/3 complex subunit 2 (ARPC2) that attenuates the rate of actin polymerization by impairing the function of Arp2/3.Benproperine phosphate inhibits cancer cell migration and tumor metastasis and has been used in studies related to cough. Benproperine phosphate inhibits cancer cell migration and tumor metastasis and can be used in cough-related studies.
M54484 Tetracosactide Tetracosactide (Tetracosactrin) is an analogue of adrenocorticotrophic hormone (ACTH), Tetracosactide can stimulate the release of corticosteroids such as cortisol from the adrenal gland.
M54403 CTP CTP is a cardiac targeting peptide.
M54397 BMP2-derived peptide BMP2-derived peptide is a functional motif from positions 73 to 92 of the amino acid sequence of BMP-2.
M54383 Gly-Arg-AMC Gly-Arg-AMC is a peptide substrate of DPAP1.
M54361 Cholecystokinin Octapeptide, desulfated Cholecystokinin Octapeptide, desulfated is a synthetic desulfated octapeptides of cholecystokinin (CCK).
M54334 MUC5AC motif peptide MUC5AC motif peptide is a 16-amino acid fragment of mucin 5.
M54259 Gly-Asp-Asp-Asp-Asp-Lys-β-naphthylamide Gly-Asp-Asp-Asp-Asp-Lys-β-naphthylamide (GD4K-na) is a substrate for human enteropeptidase (Km: 0.16 mM).
M54237 Kisspeptin-10, human Kisspeptin-10, human is a potent vasoconstrictor and inhibitor of angiogenesis.
M54221 SEB Domain (152-161) SEB Domain (152-161) is Staphylococcal Enterotoxin B domain amino acid residue 152-161.
M54188 Mca-Pro-Leu-Gly-Pro-D-Lys(Dnp) Mca-Pro-Leu-Gly-Pro-D-Lys(Dnp) is a FRET substrate of Thimet oligopeptidase.
M54157 Osteogenic Growth Peptide, OGP Osteogenic Growth Peptide, OGP is a short, naturally occurring 14-mer growth factor peptide found in serum at μM concentrations.
M53990 LQVTDSGLYRCVIYHPP LQVTDSGLYRCVIYHPP (LP17) is a triggering receptor expressed on myeloid cells (TREM-1) inhibitory peptide.
M53856 Alloferon 1 Alloferon 1 is an antiviral and antitumoral peptide.
M53713 α-Methyltyrosine methyl ester hydrochloride α-Methyltyrosine methyl ester hydrochloride is a competitive tyrosine hydroxylase inhibitor that inhibits the conversion of tyrosine to dopamine.




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