14 Results for "

allosteric regulator

" in MedChemExpress (MCE) Product Catalog:
Products (14)

14 Results for "allosteric regulator" in MCE Product Catalog:

40
40 Publications Verification
Cat. No.: HY-119374
CAS No.: 2270879-17-7
Purity:  99.72%
Target:  

SWI/SNF Complex

Research Areas:  

Cancer

BRM/BRG1 ATP Inhibitor-1 (compound 14) is an orally active allosteric dual brahma homolog (BRM)/SWI/SNF related matrix associated actin dependent regulator of chromatin subfamily A member 2 (SMARCA2) and brahma related gene 1 (BRG1)/SMARCA4 ATPase activity inhibitor, both IC50s are below 0.005 µM. BRM/BRG1 ATP Inhibitor-1 has anticancer activity .
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12
12 Cited Publications
Cat. No.: HY-103269
CAS No.: 335165-68-9
Purity:  99.89%
Target:  

Bcl-2 Family Apoptosis

Research Areas:  

Cancer

BAI1 is a selective and allosteric inhibitor of BAX, an apoptosis regulator. BAI1 directly binds to BAX and allosterically inhibits BAX activation. BAI1 has the potential for the research of diseases mediated by BAX-dependent cell death .
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2
2 Cited Publications
Cat. No.: HY-13509
CAS No.: 883050-24-6
Purity:  99.62%
Target:  

RGS Protein

Research Areas:  

Inflammation/Immunology

CCG-50014 is the most potent against the regulator of G-protein signaling protein type 4 (RGS4) (IC50 =30 nM) and is >20-fold selective for RGS4 over other RGS proteins. CCG-50014 binds covalently to the RGS, forming an adduct on two cysteine residues located in an allosteric regulatory site . CCG50014, reduces nociceptive responses and enhances opioid-mediated analgesic effects in the mouse formalin test .
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Cat. No.: HY-148788
CAS No.: 2417955-18-9
Purity:  99.83%
Synonyms: GBT-601; GBT-021601
Target:  

Hemoglobin

Research Areas:  

Others

Osivelotor is an orally effective small molecule. Osivelotor is an allosteric regulator of deoxyhemoglobin S (HbS). Osivelotor increases the affinity of HbS to oxygen, inhibits HbS polymerization, and thus prevents erythrocyte sickling in the blood. Osivelotor can be used for research of sickle cell disease (SCD) .
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Cat. No.: HY-141510
CAS No.: 23103-35-7
Purity:  ≥95.0%
Synonyms: ITPP hexasodium
Research Areas:  

Cardiovascular Disease Cancer

myo-Inositol trispyrophosphate (ITPP) hexasodium is a salt form of inositol triphosphate (ITPP). myo-Inositol trispyrophosphate (ITPP) hexasodium is a membrane-permeant hemoglobin allosteric regulator. myo-Inositol trispyrophosphate (ITPP) hexasodium enhances the oxygen release capacity of red blood cells by reducing the affinity of hemoglobin to oxygen. myo-Inositol trispyrophosphate (ITPP) hexasodium can be used in the study of cardiovascular disease and cancer .
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Cat. No.: HY-148016
CAS No.: 2014368-93-3
Purity:  99.36%
I-287 is a orally active selective PAR2 inhibitor that acting as a negative allosteric regulator on Gαq and Gα12/13 activity and their downstream effectors. I-287 reduces Complete Freund's adjuvant (HY-153808)-induced inflammation in mice and can be used for inflammation/immunology research .
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Cat. No.: HY-158991
CAS No.: 3054995-92-2
Purity:  98.06%
Target:  

CFTR

Research Areas:  

Inflammation/Immunology

I1421 is an activator of the cystic fibrosis transmembrane conductance regulator (CFTR) with an EC50 of 64 nM for WT CFTR currents. I1421 also allosterically activates multiple mutants causing cystic fibrosis (CF) with good in vivo potency, with an oral bioavailability of 60% in mice corresponding to a half-life of 75 min. I1421 synergizes with Elexacaftor (HY-111772) to enhance CFTR currents .
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Cat. No.: HY-141510A
CAS No.: 851086-77-6
Purity:  ≥98.0%
Synonyms: ITPP hexa-triethylamine
myo-Inositol trispyrophosphate (ITPP) hexa-triethylamine is a salt form of inositol triphosphate (ITPP). myo-Inositol trispyrophosphate hexa-triethylamine is a membrane-permeant hemoglobin allosteric regulator. myo-Inositol trispyrophosphate hexa-triethylamine enhances the oxygen release capacity of red blood cells by reducing the affinity of hemoglobin to oxygen. myo-Inositol trispyrophosphate hexa-triethylamine can be used in the study of cardiovascular disease and cancer .
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Cat. No.: HY-155467
Target:  

Adenosine Receptor

Research Areas:  

Endocrinology

MRS7935 (compound 15) is an A1AR positive allosteric modulator (PAM) with an EC50 of approximately 2 μM .
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Cat. No.: HY-128783
CAS No.: 312622-77-8
Target:  

mAChR

Research Areas:  

Neurological Disease

VU0090157 is a positive allosteric modulator (PAM) of the M1 muscarinic acetylcholine receptor (mAChR). VU0090157 increases the affinity of ACh by binding to the allosteric site. VU0090157 can be used in the study of schizophrenia and Alzheimer's disease .
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Cat. No.: HY-169256
CAS No.: 767310-01-0
Target:  

SARS-CoV

Research Areas:  

Infection

ZINC4497834 is an inhibitor of SARS-CoV-2 major protease Mpro. ZINC4497834 can be used in anti-COVID19 research .
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Cat. No.: HY-13509R
CAS No.: 883050-24-6
Target:  

RGS Protein

Research Areas:  

Inflammation/Immunology

CCG-50014 (Standard) is the analytical standard of CCG-50014. This product is intended for research and analytical applications. CCG-50014 is the most potent against the regulator of G-protein signaling protein type 4 (RGS4) (IC50 =30 nM) and is >20-fold selective for RGS4 over other RGS proteins. CCG-50014 binds covalently to the RGS, forming an adduct on two cysteine residues located in an allosteric regulatory site . CCG50014, reduces nociceptive responses and enhances opioid-mediated analgesic effects in the mouse formalin test .
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Cat. No.: HY-103269R
CAS No.: 335165-68-9
Research Areas:  

Cancer

BAI1 (Standard) is the analytical standard of BAI1 (HY-103269). This product is intended for research and analytical applications. BAI1 is a selective and allosteric inhibitor of BAX, an apoptosis regulator. BAI1 directly binds to BAX and allosterically inhibits BAX activation. BAI1 has the potential for the research of diseases mediated by BAX-dependent cell death .
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Cat. No.: HY-W673613
CAS No.: 1067191-08-5
Research Areas:  

Endocrinology

ADX68692 is an orally active FSHR negative allosteric regulator, with an IC50 value of 140 nM against hFSHR. ADX68692 antagonizes hCG (HY-107953)-mediated cAMP production, β-arrestin 2 recruitment, and the LH/CGR signaling pathway. ADX68692 partially inhibits testosterone synthesis. ADX68692 blocks follicle growth, disrupts the estrous cycle in rats, and reduces the pregnancy rate in rats. ADX68692 can be used in research related to contraception and endometriosis .
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