| Cat. No. |
Product Name |
Information |
| PC-28053 |
MOG(35-55) amide Mouse, Rat
MOG peptide
|
MOG(35-55) peptide (mouse/rat sequence) is a myelin oligodendrocyte glycoprotein (MOG) peptide derived from the extracellular domain of MOG protein and key immunodominant epitope extensively utilized in the study of autoimmune demyelinating diseases of the central nervous system (CNS), induce experimental autoimmune encephalomyelitis (EAE) in susceptible animal models, particularly C57BL/6 mice. |
| PC-27993 |
α-glucosidase inhibitor 9f
alpha-glucosidase inhibitor
|
α-glucosidase inhibitor 9f is a potent, competitive inhibitor of alpha-glucosidase (α-glucosidase) with IC50 of 100 nM. |
| PC-27927 |
Spinosyn D
CAS 131929-63-0
|
Spinosyn D is the active ingredient of spinosad, which is a natural pesticide against a wide variety of insect pest species. |
| PC-27926 |
Spinosad
EGFR inhibitor
|
Spinosad is a pediculicide mixture of spinosyn A and spinosyn D (in an approximately 5:1 ratio, respectively), shows selective activity against a wide variety of insect pest species, effectively suppresses cell proliferation of lung adenocarcinoma (LUAD), disrupts the interaction between CHRNA5 and EGFR. |
| PC-27925 |
Spinosyn A
ASS1 activator
|
Spinosyn A is a polyketide insecticide in Saccharopolyspora spinosa, suppresses breast tumor cell proliferation and growth by binding to and activating Argininosuccinate synthase (ASS1), has potential inhibitory effects on a variety of cancer cells. |
| PC-27923 |
3-Hydroxyhippuric acid
Kynureninase inhibitor
|
3-Hydroxyhippuric acid is an inhibitor of kynureninase (KYNU) with Ki of 60 uM, affects the spatial overflow of mtROS from mitochondria to the endoplasmic reticulum (ER). |
| PC-27917 |
Pinoresinol
β-glucuronidase inhibitor
|
Pinoresinol ((+)-Pinoresinol) is a putative hypoglycemic agent in defatted sesame (Sesamum indicum) seeds, shows inhibitory activity against rat intestinal α-glucosidase with IC50 of 34.3 uM, inhibits proliferation and induces differentiation on human HL60 leukemia cells, also exerts enzymatic β-glucuronidase inhibitory activity with IC50 of 27.9 uM. |
| PC-27845 |
Thiazolidine-2-carboxylate
PRODH inhibitor
|
Thiazolidine-2-carboxylate (T2C) is a covalent, irreversible inhibitor of proline dehydrogenase (PRODH), covalently binds to the N5 of the FAD in the PRODH domain. also inhibits pyrroline-5-carboxylate reductase 1 (PYCR1). |
| PC-27844 |
N-Propargylglycine
PRODH inhibitor
|
N-propargylglycine (N-PPG) is a covalent, irreversible suicide inhibitor of proline dehydrogenase (PRODH), activates mitochondrial PRODH decay, shows anticancer activity and brain-enhancing mitohormesis properties |
| PC-27832 |
Eflornithine hydrochloride hydrate
Ornithine decarboxylase inhibitor
|
Eflornithine hydrochloride hydrate (DFMO, MDL71782, RMI71782, α-difluoromethylornithine) is an irreversible inhibitor of ornithine decarboxylase (ODC), inhibits polyamine biosynthesis. |
| PC-27826 |
DDAH1 inhibitor A8
DDAH1 inhibitor
|
DDAH1 inhibitor A8 is a small molecule inhibitor of dimethylarginine dimethylaminohydrolase 1 (DDAH1) with IC50 of 176 uM, significantly suppresses vasculogenic mimicry in TNBC cells. |
| PC-27780 |
A8535
GPR27 agonist
|
A8535 is a selective small-molecule GPR27 (SREB1) agonist. |
