Sulfopin
CAS No. 2451481-08-4
Sulfopin( PIN1-3 )
Catalog No. M24127 CAS No. 2451481-08-4
Sulfopin is a highly selective covalent inhibitor of Pin1 with an apparent Ki of 17nM. Sulfopin blocks Myc-driven tumors in vivo.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 41 | In Stock |
|
| 5MG | 68 | In Stock |
|
| 10MG | 113 | In Stock |
|
| 25MG | 233 | In Stock |
|
| 50MG | 375 | In Stock |
|
| 100MG | 560 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameSulfopin
-
NoteResearch use only, not for human use.
-
Brief DescriptionSulfopin is a highly selective covalent inhibitor of Pin1 with an apparent Ki of 17nM. Sulfopin blocks Myc-driven tumors in vivo.
-
DescriptionSulfopin is a highly selective covalent inhibitor of Pin1 with an apparent Ki of 17nM. Sulfopin blocks Myc-driven tumors in vivo.
-
In VitroCell Proliferation Assay Cell Line:Kuramochi, MDA-MB-468, NGP, NBL-S, MDA-MB-468 cells Concentration:1, 2.5 μM Incubation Time:4,6, 8 days Result:Showed variation in antiproliferative effects across cancer cell lines Kuramochi, MDA-MB-468, NGP and NBL-S, with the most pronounced sensitivity observed in MDA-MB-468 cells.
-
In Vivo——
-
SynonymsPIN1-3
-
PathwayOthers
-
TargetOther Targets
-
RecptorPin1
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2451481-08-4
-
Formula Weight281.8
-
Molecular FormulaC11H20ClNO3S
-
Purity>98% (HPLC)
-
SolubilityDMSO : 90 mg/mL (319.38 mM; Need ultrasonic)
-
SMILESO=C(N(CC(C)(C)C)C(CC1)CS1(=O)=O)CCl
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Dubiella C , Pinch B J , Koikawa K , et al. Sulfopin is a covalent inhibitor of Pin1 that blocks Myc-driven tumors in vivo[J]. Nature Chemical Biology.
molnova catalog
related products
-
DL-5-Hydroxylysine h...
DL-5-Hydroxylysine is a racemic mixture of D- and L- enantiomers of 5-hydroxylysine which may be used as potential target markers for radical-induced protein oxidation.
-
Verdiperstat
Verdiperstat (AZD-3241) is a potent, selective, reversible, orally active myeloperoxidase (MPO) inhibitor with IC50 of 630 nM, >14-fold selectivity over thyroid peroxidase (TPO).
-
TIM-3-IN-2
TIM-3-IN-2 is a Tim3 inhibitor that inhibits the binding of TIM-3 to PtdSer, CEACAM1, and Gal-9 and inhibits the action of TIM-3.TIM-3-IN-2 is able to reverse TIM-3-mediated pro-inflammatory cytokine action.
Cart
sales@molnova.com