Cart
sales@molnova.com
T-0156
CAS No. 324572-92-1
T-0156( —— )
Catalog No. M33936 CAS No. 324572-92-1
T-0156 is a novel, potent and selective phosphodiesterase type 5 inhibitor that inhibits the hydrolysis of cyclic guanosine monophosphate (cGMP) with low affinity for PDE6, PDE1, PDE2, PDE3 and PDE4.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 321 | In Stock |
|
| 10MG | 459 | In Stock |
|
| 25MG | 718 | In Stock |
|
| 50MG | 958 | In Stock |
|
| 100MG | 1274 | In Stock |
|
| 200MG | 1721 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameT-0156
-
NoteResearch use only, not for human use.
-
Brief DescriptionT-0156 is a novel, potent and selective phosphodiesterase type 5 inhibitor that inhibits the hydrolysis of cyclic guanosine monophosphate (cGMP) with low affinity for PDE6, PDE1, PDE2, PDE3 and PDE4.
-
DescriptionT-0156 is a novel, potent and selective phosphodiesterase type 5 inhibitor that inhibits the hydrolysis of cyclic guanosine monophosphate (cGMP) with low affinity for PDE6, PDE1, PDE2, PDE3 and PDE4.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayMicrobiology/Virology
-
TargetParasite
-
RecptorParasite | PDE
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number324572-92-1
-
Formula Weight583.59
-
Molecular FormulaC31H29N5O7
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C(OC)C1=C(C=2C=C(OC)C(OC)=C(OC)C2)C=3C=CN=C(OCC4=NC=CC=N4)C3C(=O)N1CC=5C=CN=C(C5)C
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
GNF179
GNF179 is an optimized 8,8-dimethyl IP analog.
-
FR900098 sodium salt
FR 900098 is a derivative of fosmidomycin that inhibits DOXP reductoisomerase, demonstrates antimalarial activity with IC50 of 170, 170, and 90 nM for HB3, A2, and Dd2 P. falciparum strains, respectively.
-
PK 11195
PK 11195 (RP 52028) is a TSPO ligand for neuroimaging that exhibits significant protection against CoCl2-induced alterations and can be used to study leishmaniasis.
