Cart
sales@molnova.com
kb-NB77-78
CAS No. 1350622-33-1
kb-NB77-78( Kb-NB77-78 | KbNB7778 )
Catalog No. M11418 CAS No. 1350622-33-1
kb-NB77-78 is an analog of CID797718, which is a by-product of the synthesis of the parental compound, CID755673(PKD1 inhibitor).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 72 | In Stock |
|
| 5MG | 110 | In Stock |
|
| 10MG | 178 | In Stock |
|
| 25MG | 399 | In Stock |
|
| 50MG | 590 | In Stock |
|
| 100MG | 840 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Namekb-NB77-78
-
NoteResearch use only, not for human use.
-
Brief Descriptionkb-NB77-78 is an analog of CID797718, which is a by-product of the synthesis of the parental compound, CID755673(PKD1 inhibitor).
-
Descriptionkb-NB77-78 is an analog of CID797718, which is a by-product of the synthesis of the parental compound, CID755673(PKD1 inhibitor).
-
In Vitrokb-NB77-78 is an analogue of CID797718, but shows no PKD inhibitory activity.
-
In Vivo——
-
SynonymsKb-NB77-78 | KbNB7778
-
PathwayApoptosis
-
TargetSerine/threonin kinase
-
RecptorPKD1
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1350622-33-1
-
Formula Weight331.48
-
Molecular FormulaC18H25NO3Si
-
Purity>98% (HPLC)
-
SolubilitySoluble in DMSO
-
SMILESO=C(C1=C2CCCN1)OC3=C2C=C(O[Si](C)(C(C)(C)C)C)C=C3
-
Chemical Name9-((tert-butyldimethylsilyl)oxy)-1,2,3,4-tetrahydro-5H-chromeno[3,4-b]pyridin-5-one
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.George KM, et al. Pharmaceutics. 2011;3(2):186-228.
molnova catalog
related products
-
TAO Kinase inhibitor...
TAO Kinase inhibitor 2 is a TAO kinase inhibitor with an IC50 of 50-500 nM. TAO Kinase inhibitor 2 inhibits KIAA1361 and JIK with IC50s of 50-500 nM.
-
IPR-803
IPR-803 is an effective inhibitor of the uPAR·uPA protein-protein interaction (PPI) with anti-tumor activity. IPR-803 binds directly to uPAR with a Ki of 0.2 μM.
-
HA-1004
HA-1004 is a inhibitor of PKG, PKA, PKC and MLC.
