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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
99 Results for "
PKB
" in MedChemExpress (MCE) Product Catalog:
Products (99)
99 Results for "PKB" in MCE Product Catalog:
657
657 Publications Verification
Synonyms: SB 203580; RWJ 64809
Áreas de investigación:
Adezmapimod (SB 203580) is a selective and ATP-competitive p38 MAPK inhibitor with IC50s of 50 nM and 500 nM for SAPK2a/p38 and SAPK2b/p38β2, respectively. Adezmapimod inhibits LCK, GSK3β and PKBα with IC50s of 100-500-fold higher than that for SAPK2a/p38. Adezmapimod can inhibit p38 MAPK and lead to the inhibition of downstream HSP27 phosphorylation. Adezmapimod does not disrupt JNK activity and is an autophagy and mitophagy activator .
657
657 Publications Verification
Synonyms: SB 203580 hydrochloride; RWJ 64809 hydrochloride
Áreas de investigación:
Adezmapimod (SB 203580; RWJ 64809) hydrochloride is a selective and ATP-competitive p38 MAPK inhibitor with IC50s of 50 nM and 500 nM for SAPK2a/p38 and SAPK2b/p38β2, respectively. Adezmapimod hydrochloride inhibits LCK, GSK3β and PKBα with IC50s of 100-500-fold higher than that for SAPK2a/p38. Adezmapimod hydrochloride does not disrupt JNK activity and is an autophagy and mitophagy activator .
14
Target:
Áreas de investigación:
SB-334867 (SB 334867A) is an excellent,selective and blood-brain barrier permeable orexin-1 (OX1) receptor antagonist, shows selectivity over OX2 (pKb=7.4), 100-fold over 5-HT2B, 5-HT2C with pKi values of 5.4 and 5.3, respectively . SB-334867 reduces ethanol consumption and inhibits the acquisition of morphine-induced sensitization to locomotor activity in vivo .
14
14 Cited Publications
Synonyms: SB334867A free base
Target:
Áreas de investigación:
SB-334867 free base (SB334867A free base) is an excellent, selective and blood–brain barrier permeable orexin-1 (OX1) receptor antagonist, shows selectivity over OX2 (pKb=7.4), 100-fold over 5-HT2B, 5-HT2C with pKi values of 5.4 and 5.3, respectively . SB-334867 reduces ethanol consumption and inhibits the acquisition of morphine-induced sensitization to locomotor activity in vivo .
9
9 Cited Publications
Target:
Áreas de investigación:
GR 113808 is a potent and highly selective 5-HT4 receptor antagonist (pKb= 8.8). GR 113808 shows 300-fold selectivity over 5-HT1A, 5-HT1B, 5-HT2A, 5-HT2C and 5-HT3 receptors .
4
4 Cited Publications
Referencia número: HY-P80276
Synonyms: AKT 1 antibody; AKT antibody; AKT1 antibody; AKT1_HUMAN antibody; MGC99656 antibody; PKB antibody; PKB-ALPHA antibody; PRKBA antibody; Protein Kinase B Alpha antibody; Protein kinase B antibody; Proto-oncogene c-Akt antibody; RAC Alpha antibody; RAC antibody; RAC-alpha serine/threonine-protein kinase antibody; RAC-PK-alpha antibody;
3
3 Cited Publications
Referencia número: HY-N1401
No. CAS: 112246-15-8
2
2 Cited Publications
Referencia número: HY-P80789
Synonyms: AKT1; AKT2; AKT3; PKB; RAC; RAC-alpha serine/threonine-protein kinase; Protein kinase B; PKB; Protein kinase B alpha; PKB alpha; Proto-oncogene c-Akt; RAC-PK-alpha
1
Target:
Áreas de investigación:
Hematein is a oxidation product of hematoxylin acted as a dye . Hematein is an allosteric casein kinase II inhibitor with an IC50 of 0.74 μM. Hematein inhibits Akt/PKB Ser129 phosphorylation, the Wnt/TCF pathway and increases apoptosis in lung cancer cells .
1
1 Cited Publications
API-1 is a potent selective Akt/PKB inhibitor that reduces the level of phosphorylated Akt (IC50 = 0.8 μM). API-1 binds to the PH domain and inhibits Akt membrane translocation. API-1 induces c-FLIP degradation. API-1 reduces cell proliferation and induces apoptosis. API-1 decreases tumor growth in mouse xenograft model .
1
1 Cited Publications
Target:
Áreas de investigación:
MRS2279 diammonium is a selective and high affinity P2Y1 receptor antagonist, with a Ki value of 2.5 nM and an IC50 value of 51.6 nM. MRS2279 diammonium competitively inhibits ADP-promoted platelet aggregation with an pKb value of 8.05 .
1
1
1 Cited Publications
Referencia número: HY-P702631
Pureza: ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: AKT1; Protein Kinase B; AKT Serine/Threonine Kinase 1; PKB Alpha; RAC; V-Akt Murine Thymoma Viral Oncogene-Like Protein 1 Isoform 2; PKB; V-Akt Murine Thymoma Viral Oncogene-Like Protein 1; RAC-Alpha Serine/Threonine-Protein Kinase; Non-Specific Serine/Threonine Protein Kinase; RAC-PK-Alpha; AKT1m Transcript Variant 3; RAC-Alpha; AKT1m Transcript Variant 4; PRKBA; AKT1m Transcript Variant 2; AKT; AKT1m Transcript Variant 1; V-Akt Murine Thymoma Viral Oncogene Homolog 1; Rac Protein Kinase Alpha; Serine-Threonine Protein Kinase; PKB-ALPHA; Protein Kinase B Alpha; AKT1m; Proto-Oncogene C-Akt
Species:
Human
Source:
Sf9 insect cells
1
1
1 Cited Publications
Referencia número: HY-P74420
Pureza: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: AKT2; Non-Specific Serine/Threonine Protein Kinase; AKT Serine/Threonine Kinase 2; Murine Thymoma Viral (V-Akt) Homolog-2; V-Akt Murine Thymoma Viral Oncogene Homolog 2; Rac Protein Kinase Beta; RAC-Beta Serine/Threonine-Protein Kinase; RAC Protein Kinase Beta; Protein Kinase B Beta; AKT2 Protein; Protein Kinase Akt-2; RAC-BETA; RAC-PK-Beta; PKBBETA; PKB Beta; HIHGHH; PKBB; PRKBB; Putative V-Akt Murine Thymoma Viral Oncoprotein 2; PKBβ
Species:
Human
Source:
Sf9 insect cells
Target:
Áreas de investigación:
SB 243213 is an orally active, selective and high-affinity 5-HT2C receptor antagonist with a pKi of 9.37 and a pKb of 9.8 for human 5-HT2C receptor. SB 243213 shows greater than a 100-fold selectivity over a wide range of neurotransmitter receptors, enzymes and ion channels. SB 243213 has improved anxiolytic profile and has the potential for schizophrenia and motor disorders .
Target:
Áreas de investigación:
MIPS521 is a positive allosteric modulator of adenosine A1 receptor (A1AR). MIPS521 also has a lower A1R allosteric affinity (pKB=4.95; KB=11 μM). MIPS521 exhibits pain-relieving effects in vivo through modulation of the increased levels of endogenous adenosine .
Target:
Áreas de investigación:
Cyclopentolate (DL-Cyclopentolate) hydrochloride is an Atropine-like muscarinic receptors antagonist with a pKB value of 7.8 (on the circular ciliary muscle). Cyclopentolate hydrochloride is an anti-muscarinic agent commonly used in the ophthalmologic practice .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
