DIM-C-pPhOCH3
CAS No. 33985-68-1
DIM-C-pPhOCH3( DIM-C-pPhOCH3 | DIM C pPhOCH3 | DIM-C-pPhOMe )
Catalog No. M18439 CAS No. 33985-68-1
DIM-C-pPhOCH3 is a Nerve Growth Factor-Induced Bα (NGFI-Bα, Nur77) agonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 67 | In Stock |
|
| 5MG | 61 | In Stock |
|
| 10MG | 92 | In Stock |
|
| 25MG | 155 | In Stock |
|
| 50MG | 230 | In Stock |
|
| 100MG | 323 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameDIM-C-pPhOCH3
-
NoteResearch use only, not for human use.
-
Brief DescriptionDIM-C-pPhOCH3 is a Nerve Growth Factor-Induced Bα (NGFI-Bα, Nur77) agonist.
-
DescriptionDIM-C-pPhOCH3 is a Nur77 agonist. It has been shown to induce apoptosis in cancer cell lines and long-term potentiation in hippocampal slices and long-term contextual fear memory in an in vivo mouse mode.
-
In VitroDIM-C-pPhOCH3 decreases survival and induces apoptosis in RKO colon cancer cells, and this is accompanied by induction of tumor necrosis factor–related apoptosis-inducing ligand (TRAIL) protein. DIM-C-pPhOCH3 also induces Nur77-independent apoptosis. DIM-C-pPhOCH3 (10 μM) inhibits cell growth after treatment for 24, 48, or 72 h, and the maximum inhibitory response is observed after 72 h, where there is considerable cell detachment and dead cells. The growth-inhibitory effects observed for DIM-C-pPhOCH3 after 72 h are also accompanied by several markers of apoptosis, including PARP cleavage and cleavage of caspase-3, caspase-9, and caspase-8. PARP cleavage is also observed after treatment of RKO cells for 48 h with DIM-C-pPhOCH3.
-
In VivoDIM-C-pPhOCH3 (25 mg/kg/d) also inhibits tumor growth in athymic nude mice bearing RKO cell xenografts. The effects of DIM-C-pPhOCH3 (25 mg/kg/d) on colon tumor growth are also investigated in athymic nude mice bearing RKO cell xenografts. Treatment with the DIM-C-pPhOCH3 significantly decreases tumor volumes and final tumor weights compared with corn oil controls.
-
SynonymsDIM-C-pPhOCH3 | DIM C pPhOCH3 | DIM-C-pPhOMe
-
PathwayOthers
-
TargetOther Targets
-
RecptorNur77
-
Research AreaInflammation/Immunology
-
Indication——
Chemical Information
-
CAS Number33985-68-1
-
Formula Weight352.44
-
Molecular FormulaC24H20N2O
-
Purity>98% (HPLC)
-
SolubilityDMSO : ≥ 33.3 mg/mL; 94.49 mM
-
SMILESCOc1ccc(cc1)C(c3cnc2ccccc23)c5cnc4ccccc45
-
Chemical Name3,3'-((4-methoxyphenyl)methylene)bis(1H-indole)
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
V116517
V116517 is a potent, orally active transient receptor potential vanilloid (TRPV1) antagonist. V116517 shows potent activity in inhibiting both capsaicin (CAP)- and acid (pH 5)-induced currents in rat DRG neurons expressing native TRPV (IC50=423.2 nM for CAP; IC50=180.3 nM for acid). V116517 can be used for the research of pain.
-
Rat CGRP-(8-37)
CGRP-(8-37) is a truncated version of calcitonin gene-related peptide (CGRP) that binds to the CGRP receptor with similar affinity but does not activate the receptor,It is a highly selective CGRP receptor antagonist.
-
Vercirnon
Vercirnon is a selective and potent antagonist of CCR9 (IC50: 10 nM). It is also used in the research of inflammatory bowel diseases.
Cart
sales@molnova.com