62 Results for "

3r1

" in MedChemExpress (MCE) Product Catalog:
Products (62)

62 Results for "3r1" in MCE Product Catalog:

45
45 Publications Verification
Cat. No.: HY-15917
CAS No.: 3483-12-3
Synonyms: DTT; rel-(2R,3R)-1,4-Dimercapto-2,3-butanediol
DL-Dithiothreitol (DTT) is a strong reductant with anti-disulfidptosis activity. When DL-Dithiothreitol is oxidized, it forms a stable six-membered ring with an internal disulfide bond .
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8
8 Cited Publications
Cat. No.: HY-P80846
Synonyms: PIK3r1; GRB1; Phosphatidylinositol 3-kinase regulatory subunit alpha; PI3-kinase regulatory subunit alpha; PI3K regulatory subunit alpha; PtdIns-3-kinase regulatory subunit alpha; Phosphatidylinositol 3-kinase 85 kDa regulatory subunit alpha; PI3-kinase s

Host:  

Rabbit

Application:  

WB, IHC-F, IHC-P, ICC/IF, ELISA

Reactivity:  

Human, Mouse, Rat

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4
4 Cited Publications
Cat. No.: HY-P80867
Synonyms: PIK3r1; GRB1; Phosphatidylinositol 3-kinase regulatory subunit alpha; PI3-kinase regulatory subunit alpha; PI3K regulatory subunit alpha; PtdIns-3-kinase regulatory subunit alpha; Phosphatidylinositol 3-kinase 85 kDa regulatory subunit alpha; PI3-kinase s

Host:  

Mouse

Application:  

WB, IHC-P

Reactivity:  

Human, Mouse, Rat

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1
1 Cited Publications
Cat. No.: HY-129139
CAS No.: 111613-04-8
Purity:  95.71%
Cyanidin-3-O-arabinoside is a p38 MAPK phosphorylation inhibitor. Cyanidin-3-O-arabinoside reduces the expression of VDAC1, inhibits mtROS accumulation, reverses cellular senescence, blocks excessive mitochondrial calcium influx, reduces the formation of mitochondria-associated endoplasmic reticulum membranes, and suppresses the VDAC1-IP3R1 interaction. Cyanidin-3-O-arabinoside activates hair follicle stem cell proliferation and improves the condition of slowed hair growth. Cyanidin-3-O-arabinoside is applicable to research related to colon cancer and androgenetic alopecia .
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1
1 Cited Publications
Cat. No.: HY-108495
CAS No.: 1345858-76-5
Purity:  ≥98.0%
Synonyms: ML248
Target:  

LPL Receptor

Research Areas:  

Cardiovascular Disease

CYM50308 (ML248) is a potent, selective and high affinity sphingosine-1-phosphate receptor 4 (S1P4-R) agonist with an EC50 of 56 nM. CYM50308 displays 37-fold more selective for S1P4-R than S1P5-R. CYM50308 has no activity at S1P1-R, S1P2-R and S1P3-R subtypes at concentrations up to 25 μM .
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1
1 Cited Publications
Cat. No.: HY-P701153
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: EBP50; NHERF; NHERF-1; NHERF1; NPHLOP2
Species:  
Source:  
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Cat. No.: HY-P10849
CAS No.: 3061802-23-8
Target:  

Calcium Channel

Research Areas:  

Others

IP3RPEP6 is an IP3R competitive inhibitor. IP3RPEP6 has the IC50 values of 9.0 μM, 3.9 μM and 4.3 μM for IP3R1, IP3R2 and IP3R3, respectively. IP3RPEP6 does not affect the Ryanodine receptor and Cx43 hemichannels. IP3RPEP6 regulates calcium signaling within cells .
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Cat. No.: HY-108494
CAS No.: 1355026-60-6
Purity:  99.70%
Target:  

LPL Receptor

Research Areas:  

Cardiovascular Disease

CYM50260 is a potent and exquisitely selective sphingosine-1-phosphate 4 receptor (S1P4-R) agonist with an EC50 of 45 nM. CYM50260 displays no activity against S1P1-R, S1P2-R, S1P3-R and S1P5-R .
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Cat. No.: HY-40041
CAS No.: 163765-44-4
(R)-1-Boc-3-methyl-piperazine (Compound I3-1) is a chemical intermediate. (R)-1-Boc-3-methyl-piperazine can be used for the preparation of Compound I3. Compound I3 exhibits anticancer activity against colorectal adenocarcinoma with BRCA2 gene deletion .
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Cat. No.: HY-W111383
CAS No.: 193693-65-1
Synonyms: (R)-1-Fmoc-3-pyrrolidinecarboxylic acid
Target:  

Drug Intermediate

Research Areas:  

Others

Fmoc-D-β-Pro-OH ((R)-1-Fmoc-3-pyrrolidinecarboxylic acid) is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-40097
CAS No.: 147081-49-0
(R)-1-Boc-3-aminopyrrolidine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-P11540
CAS No.: 2923120-30-1
CCKBR agonist-1 (Compound 3r1) is a Gq-protein-preferring cholecystokinin B receptor (CCKBR) agonist with an EC50 of 35 pM. CCKBR agonist-1 significantly increases the survival rate of neurons, with an EC50 of 37 pM. CCKBR agonist-1 can improve the cognitive decline in mice by upregulating α-secretase (ADAM10) and calcium signaling molecule PLCB4, reduce the number of amyloid β () plaques, and promote long-term potentiation (LTP). CCKBR agonist-1 can be used for the study of Alzheimer's disease .
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Cat. No.: HY-162774A
Target:  

Apoptosis

Research Areas:  

Cancer

GRP75-IN-1 hydrochloride (compound 33) is an anti-endometrial cancer (EC) agent that induces apoptosis. GRP75-IN-1 hydrochloride reduces Ca 2+ levels in mitochondria by targeting GRP75 and disrupting its interaction with IP3R .
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Cat. No.: HY-111501
CAS No.: 1429375-54-1
Purity:  99.82%
Target:  

Histamine Receptor

H4R antagonist 1 is a potent and highly selective histamine H4 receptor (H4R) antagonist with an IC50 of 27 nM. H4R antagonist 1 does not show any noticeable binding affinity to other subtypes of histamine receptors, H1R, H2R, and H3R .
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Cat. No.: HY-P3862
CAS No.: 110880-53-0
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease Endocrinology

[MePhe7]-Neurokinin B is an neurokinin NK-3 receptor (NK3R) agonist with an IC50 value of 3 nM. [MePhe7]-Neurokinin B is a potential regulator of pulsatile gonadotropin-releasing hormone (GnRH) secretion via activation of the neurokinin-3 receptor (NK3R) .
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Cat. No.: HY-103178
CAS No.: 252979-43-4
Purity:  98.34%
Target:  

Adenosine Receptor

Research Areas:  

Inflammation/Immunology

MRE3008F20 is a highly efficient, highly selective and radioactive adenosine A3 receptor (AA3R) antagonist (Ki=1.8 nM). MRE3008F20 effectively antagonises Cl-IB-MECA-induced cAMP production in resting lymphocytes with an IC50 value of 5 nM. MRE3008F20 can be used in the study of AA3R .
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Cat. No.: HY-161366
CAS No.: 3033806-03-7
Target:  

PI3K

Research Areas:  

Cancer

OMS14 is exhibits inhibitory activity for phosphoinositide 3-kinase γ (PI3Kγ) and PIK3CD/PIK3R1, which inhibits 19% PI3Kγ and 65% PIK3CD/PIK3R1 activity at 100 μM. OMS14 exhibits anticancer efficacy in various cancer cells .
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Cat. No.: HY-W590670
CAS No.: 121459-06-1
Synonyms: N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]icosanamide
C20-Dihydroceramide is a biochemical assay reagent.
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Cat. No.: HY-100617A
CAS No.: 7292-81-1
Synonyms: (RS)-4-Carboxyphenylglycine
Target:  

mGluR

Research Areas:  

Others

(RS)-4CPG ((RS)-4-Carboxyphenylglycine) is a type I metabotropic glutamate receptor antagonist with activity in blocking LTP induction. In mice lacking IP3R1, (RS)-4CPG (500μM) nearly blocked long-term potentiation (LTP) induced by type I metabotropic glutamate receptor activation, with LTP of 117.6±1.7% (n = 8) in IP3R1(-/-) mice and 116.9±1.8% (n = 5) in IP3R1(+/+) mice.
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Cat. No.: HY-40062
CAS No.: 928025-57-4
Target:  

Drug Intermediate

Research Areas:  

Others

(R)-1-Boc-3-propylpiperazine is a drug intermediate for synthesis of various active compounds.
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