Cart
sales@molnova.com
THP104c
CAS No. 877792-12-6
THP104c( —— )
Catalog No. M28895 CAS No. 877792-12-6
THP104c is an inhibitor of mitochondrial fission.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 268 | In Stock |
|
| 5MG | 242 | In Stock |
|
| 10MG | 377 | In Stock |
|
| 25MG | 630 | In Stock |
|
| 50MG | 879 | In Stock |
|
| 100MG | 1190 | In Stock |
|
| 200MG | 1600 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameTHP104c
-
NoteResearch use only, not for human use.
-
Brief DescriptionTHP104c is an inhibitor of mitochondrial fission.
-
DescriptionTHP104c is an inhibitor of mitochondrial fission.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorNav1.7 channel
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number877792-12-6
-
Formula Weight376.43
-
Molecular FormulaC20H16N4O2S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (265.65 mM)
-
SMILESCOc1cccc(\C=N\Nc2ncnc3scc(-c4ccccc4)c23)c1O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Lin Z, et, al. Biophysical and Pharmacological Characterization of Nav1.9 Voltage Dependent Sodium Channels Stably Expressed in HEK-293 Cells. PLoS One. 2016 Aug 24;11(8):e0161450.
molnova catalog
related products
-
MID-1
MID-1 is an inhibitor of MG53-IRS-1 (Mitsugumin 53-Insulin Receptor Substrate-1) interaction.?It disrupts molecular association of MG53 with IRS-1 and abolishes MG53-induced IRS-1 ubiquitination and degradation in skeletal muscle, leading to elevated IRS-1 expression level and increased insulin signaling and glucose uptake.
-
(+)-JQ1 PA
(+)-JQ1 PA is a derivative of the Bromodomain and extra-terminal (BET) inhibitor JQ1, with an IC50 of 10.4 nM.
-
GKI-1
GKI-1 is a Greatwall (GWL) kinase inhibitor with an IC50 of 4.9 for hGWLFL and 2.5 μM for hGWL-KinDom. It exhibits stronger inhibition on ROCK1 with an IC50 of 11 μM and only weakly inhibits PKA.
