Phosphatase
Products Related to Phosphatase(93)
- GC70779Pimecrolimus hydrateCAS: 1000802-56-1
Pimecrolimus hydrate (SDZ-ASM 981 hydrate) is a potent, nonsteroid and orally active calcineurin inhibitor.
- GC71216PFKFB3-IN-2CAS: 794552-84-4Purity: >99.00%
PFKFB3-IN-2 is a 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (PFKFB3) inhibitor.
- GC71420ALP/Carbonic anhydrase-IN-1CAS: 2091887-74-8Purity: >99.00%
ALP/Carbonic anhydrase-IN-1 (Compound 1e) is a dual carbonic anhydrase (CA) and alkaline phosphatase (ALP) inhibitor.
- GC73072Phosphoglycolic acid lithium
Phosphoglycolic acid (lithium) is a competitive inhibitor of phosphoglycerate mutase (PGAM)-B, an enzyme of the glycolytic pathway.
- GC73467PTPN2/1-IN-2CAS: 2407611-02-1Purity: >99.00%
PTPN2/1-IN-2 is a PTPN2/1 antagonist that can be used in various tumor research.
- GC74184(R)-Azasetron besylateCAS: 2025360-91-0Purity: >98.00%
(R)-Azasetron besylate (SENS-401) is an orally active calcineurin inhibitor.
- GC79577PFKFB4-IN-1CAS: 2664831-55-2Purity: >99.50%
PFKFB4-IN-1 is a potent and selective ATP-competitive PFKFB4 inhibitor ( IC 50 = 4.50 μM) that reduces intracellular PFKFB4 protein levels.
- GC79676PTPRO-IN-1Purity: >98%
PTPRO-IN-1 is a selective, orally active PTPRO inhibitor with an IC 50 of 0.16 μM.
- GC79739(R,S)-PhosphonsaeureCAS: 25881-35-0Purity: >99.50%
(R,S)-Phosphonsaeure (Compound 2A) is an inhibitor of prostatic acid phosphatase with an IC 50 value of 4 nM.
- GC79742Anti-Rat pan-CD45 Antibody (OX1)Purity: >99.00%
Anti-Rat pan-CD45 Antibody (OX1) reacts with a common epitope present on all isotypes of rat CD45.
- GC79749SHIP1-IN-1CAS: 3027375-00-1Purity: >99.50%
SHIP1-IN-1 is an orally active, blood-brain barrier-permeable SHIP1 ligand.
- GC81703NAZ2329 (Standard)CAS: 2809469-05-2Purity: >98.00%
NAZ2329 (Standard) is the analytical standard of NAZ2329.
- GC81737Hydrocortisone phosphate sodium (Standard)CAS: 6000-74-4Purity: >98.00%
Hydrocortisone phosphate sodium (Standard) is the analytical standard of Hydrocortisone phosphate sodium.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC70779 | Pimecrolimus hydrate | 1000802-56-1 | - | |
Pimecrolimus hydrate (SDZ-ASM 981 hydrate) is a potent, nonsteroid and orally active calcineurin inhibitor. | ||||
| GC71216 | PFKFB3-IN-2 | 794552-84-4 | >99.00% | |
PFKFB3-IN-2 is a 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (PFKFB3) inhibitor. | ||||
| GC71420 | ALP/Carbonic anhydrase-IN-1 | 2091887-74-8 | >99.00% | |
ALP/Carbonic anhydrase-IN-1 (Compound 1e) is a dual carbonic anhydrase (CA) and alkaline phosphatase (ALP) inhibitor. | ||||
| GC72918 | BN-82685 | 477603-18-2 | >95.00% | |
BN-82685 is a a quinone-based CDC25 inhibitor with IC50 of 201 nM, 117 nM, 109 nM, 160 nM, 249 nM, for CDC25C, CDC25C-cat, CDC25A, CDC25B2, CDC25B3, respectively. | ||||
| GC72952 | 1E7-03 | 1565845-92-2 | >95.00% | |
1E7-03, a low MW tetradroquinoline derivative targeting protein phosphatase-1, can inhibit HIV-1 transcription. | ||||
| GC73020 | M5N36 | 2832887-40-6 | - | |
M5N36 is a potent and selective Cdc25C inhibitor with IC50 values of 0.15, 0.19, 0.06 µM for Cdc25A, Cdc25B, Cdc25C, respectively. | ||||
| GC73072 | Phosphoglycolic acid lithium | - | - | |
Phosphoglycolic acid (lithium) is a competitive inhibitor of phosphoglycerate mutase (PGAM)-B, an enzyme of the glycolytic pathway. | ||||
| GC73467 | PTPN2/1-IN-2 | 2407611-02-1 | >99.00% | |
PTPN2/1-IN-2 is a PTPN2/1 antagonist that can be used in various tumor research. | ||||
| GC73572 | PP5-IN-1 | 1022417-69-1 | >99.00% | |
PP5-IN-1 (Compound P053) is a competitive inhibitor of Serine/threonine protein phosphatase-5 (PP5) that binds to its catalytic domain and causes apoptosis in renal cancer. | ||||
| GC73595 | LYP-IN-3 | - | >99.00% | |
LYP-IN-3 (compound D34) is a selective inhibitor of Lymphoid-tyrosine phosphatase (LYP) (Ki=0.93 μM), and regulates T-cell receptor (TCR) signaling pathway in tumor progress. | ||||
| GC74184 | (R)-Azasetron besylate | 2025360-91-0 | >98.00% | |
(R)-Azasetron besylate (SENS-401) is an orally active calcineurin inhibitor. | ||||
| GC79230 | BBO-11818 | 3029443-36-2 | >99.50% | |
BBO-11818 is an orally active, highly selective (relative to NRAS and HRAS ), non-covalent pan- KRAS inhibitor ( IC 50 =28-120 nM). | ||||
| GC79577 | PFKFB4-IN-1 | 2664831-55-2 | >99.50% | |
PFKFB4-IN-1 is a potent and selective ATP-competitive PFKFB4 inhibitor ( IC 50 = 4.50 μM) that reduces intracellular PFKFB4 protein levels. | ||||
| GC79676 | PTPRO-IN-1 | - | >98% | |
PTPRO-IN-1 is a selective, orally active PTPRO inhibitor with an IC 50 of 0.16 μM. | ||||
| GC79739 | (R,S)-Phosphonsaeure | 25881-35-0 | >99.50% | |
(R,S)-Phosphonsaeure (Compound 2A) is an inhibitor of prostatic acid phosphatase with an IC 50 value of 4 nM. | ||||
| GC79740 | ML 086 | 1177148-36-5 | >98% | |
ML 086 is a highly selective PHOSPHO1 phosphatase inhibitor ( IC 50 =0.14 μM). | ||||
| GC79741 | KF-52 enantiomer | 3104612-73-6 | >98.50% | |
KF-52 enantiomer is an enantiomer of KF-52. | ||||
| GC79742 | Anti-Rat pan-CD45 Antibody (OX1) | - | >99.00% | |
Anti-Rat pan-CD45 Antibody (OX1) reacts with a common epitope present on all isotypes of rat CD45. | ||||
| GC79749 | SHIP1-IN-1 | 3027375-00-1 | >99.50% | |
SHIP1-IN-1 is an orally active, blood-brain barrier-permeable SHIP1 ligand. | ||||
| GC81703 | NAZ2329 (Standard) | 2809469-05-2 | >98.00% | |
NAZ2329 (Standard) is the analytical standard of NAZ2329. | ||||
| GC81737 | Hydrocortisone phosphate sodium (Standard) | 6000-74-4 | >98.00% | |
Hydrocortisone phosphate sodium (Standard) is the analytical standard of Hydrocortisone phosphate sodium. | ||||