Piperazines

eMolecules​ 129830-38-2 | Medchem Express | Y-27632 (dihydrochloride) | 10mg | 446258908 | HY-10583 | MFCD03490488 | 320.26 | C14H23Cl2N3O

Ambeed | 3-(Cyclopropylmethoxy)-4-(difluoromethoxy)benzaldehyde | 250mg | 521427998 | A243077 | 151103-09-2 | MFCD07779381 | 242.222 | C12H12F2O3

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Apexbio Technology LLC MPP dihydrochloride(Synonyms: MPP dihydrochloride, Methyl-piperidino-pyrazole dihydrochloride, ER-alpha antagonist MPP), 10mg, CAS: 911295-24-4.

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MPP dihydrochloride (CAS 911295-24-4) is a selective modulator of estrogen receptor (ER) activity demonstrating both agonist and antagonist properties Through modulation of ER-mediated signaling pathways this compound counteracts the biological effects driven by -estradiol inducing apoptosis specifically in ovarian and endometrial cancer cell types Due to its targeted interaction with ER MPP dihydrochloride serves as a research tool for investigating estrogen receptor pathways and their implications in oncology

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eMolecules​ 57260-71-6 | Tert-Butyl 1-Piperazinecarboxylate | AA Blocks LLC | MFCD00075265 | 186.255 | C9H18N2O2 | 0.000 | CC(C)(C)OC(=O)N1CCNCC1 | 5g | 497021906

Tert-Butyl 1-Piperazinecarboxylate | AA Blocks LLC | 57260-71-6 | MFCD00075265 | 186.255 | C9H18N2O2 | 0.000 | CC(C)(C)OC(=O)N1CCNCC1 | 5g | 497021906

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Ambeed TERT-BUTYL PIPERAZINE-1-100G

tert-Butyl piperazine-1-carboxylate, 100G, CAS# 57260-71-6, MOLWT: 186.25, MFCD00075265,

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Apexbio Technology LLC IT1t dihydrochloride 1092776-63-0 50mg

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IT1t dihydrochloride (CAS 1092776-63-0) is a small-molecule antagonist targeting the chemokine receptor CXCR4 It is designed to inhibit CXCR4-mediated signaling by disrupting interactions with its natural ligand CXCL12 as well as the HIV envelope protein gp120 thereby interfering with cellular chemotaxis and viral entry mechanisms IT1t dihydrochloride exerts its biological activity primarily by antagonizing CXCR4 to inhibit receptor-mediated Ca2 mobilization and virus attachment In in vitro assays IT1t dihydrochloride demonstrates potent inhibition with IC50 values of approximately 8 nM in human CXCR4 receptor binding assays 1 1 nM in Ca2 mobilization assays and 7 nM in HIV attachment assays Based on these pharmacological properties IT1t dihydrochloride holds research potential in CXCR4-related signaling and HIV entry studies

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Medchemexpress LLC Benzyl-piperazine-co-benzothiazole-4-methylpiperidine | 906258-48-8 | 99.0% | 434.60 | C25H30N4OS | 5 MG

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Benzyl-piperazine-CO-benzothiazole-4-methylpiperidine is a small-molecule research reagent reported to alter lifespan in eukaryotic organisms. It is supplied as a high-purity solid intended for laboratory research use only and is typically handled and stored under standard compound management conditions.

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Medchemexpress LLC N-(tert-Butoxycarbonyl)-N-methyl-D-leucine | 89536-84-5 | 97.0% | 245.32 | 100 G

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N-(tert-Butoxycarbonyl)-N-methyl-D-leucine is a leucine derivative, intended for research use only, not for sale to patients. Amino acids and amino acid derivatives, such as this product, are commercially utilized as ergogenic supplements. They are known to influence anabolic hormone secretion, fuel supply during exercise, mental performance under stress, and help prevent exercise-induced muscle damage, making them beneficial ergogenic dietary substances.

• Leucine derivative
• Influences anabolic hormone secretion
• Supplies fuel during exercise
• Improves mental performance during stress-related tasks
• Prevents exercise-induced muscle damage
• Used as an ergogenic supplement
• Related to amino acids and derivatives
• Used as reagents for peptide synthesis
• Classified under peptides

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eMolecules​ 1416439-26-3 | 8-BENZYL-3,8-DIAZABICYCLO[4.2.0]OCTANE | AstaTech | MFCD22690157 | 202.301 | C13H18N2 | 95.000 | C(N1CC2CCNCC12)c1ccccc1 | 1g | 200615541

8-BENZYL-3,8-DIAZABICYCLO[4.2.0]OCTANE | AstaTech | 1416439-26-3 | MFCD22690157 | 202.301 | C13H18N2 | 95.000 | C(N1CC2CCNCC12)c1ccccc1 | 1g | 200615541

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eMolecules​ 110-85-0 | Piperazine | Apollo Scientific US | MFCD00005953 | 86.138 | C4H10N2 | 97.000 | C1CNCCN1 | 100g | 686668683

Piperazine | Apollo Scientific US | 110-85-0 | MFCD00005953 | 86.138 | C4H10N2 | 97.000 | C1CNCCN1 | 100g | 686668683

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eMolecules​ 138775-03-8 | (2S)-4-benzyloxycarbonyl-1-tert-butoxycarbonyl-piperazine-2-carboxylic acid | Pharmablock | MFCD02179111 | 364.398 | C18H24N2O6 | 97.000 | CC(C)(C)OC(=O)N1CCN(C[C@H]1C(O)=O)C(=O)OCc1ccccc1 | 2.5g | 686927922

(2S)-4-benzyloxycarbonyl-1-tert-butoxycarbonyl-piperazine-2-carboxylic acid | Pharmablock | 138775-03-8 | MFCD02179111 | 364.398 | C18H24N2O6 | 97.000 | CC(C)(C)OC(=O)N1CCN(C[C@H]1C(O)=O)C(=O)OCc1ccccc1 | 2.5g | 686927922

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TARGETMOL CHEMICALS INC LM11A-31 dihydrochloride 50MG

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Also available in 10 mg, 25 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. LM11A-31 dihydrochloride is a water-soluble, non-peptide with high blood-brain barrier permeability.LM11A-31 dihydrochloride, a p75NTR (neurotrophin receptor p75) Ligand, is a potent proNGF (nerve growth factor) antagonist. Purity 98%

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eMolecules​ 141302-36-5 | 5-Bromo-2-(4-methylpiperazin-1-yl)pyrimidine | MFCD03646018 | 1g

Pharmablock | methyl 4-(aminomethyl)benzoate | 25mg | 784546181 | PBJZHC151 | 18469-52-8 | MFCD00468795 | 165.192 | C9H11NO2

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eMolecules​ 93428-55-8 | 8-BENZYL-3,8-DIAZABICYCLO[3.2.1]OCTANE 2HCL | AstaTech | MFCD23135612 | 275.220 | C13H20Cl2N2 | 95.000 | Cl.Cl.C(N1C2CCC1CNC2)c1ccccc1 | 1g | 449748365

8-BENZYL-3,8-DIAZABICYCLO[3.2.1]OCTANE 2HCL | AstaTech | 93428-55-8 | MFCD23135612 | 275.220 | C13H20Cl2N2 | 95.000 | Cl.Cl.C(N1C2CCC1CNC2)c1ccccc1 | 1g | 449748365

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Selleck Chemical LLC HA-100 dihydrochloride S2964-25mg

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HA-100 dihydrochloride is an inhibitor of cGMP-dependent protein kinase (PKG) cAMP-dependent protein kinase (PKA) protein kinase C (PKC) and MLC-kinase with IC50 of 4 M 8 M 12 M and 240 M respectively

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Medchemexpress LLC MPP dihydrochloride | 911295-24-4 | MFCD06411603 | 99.5% | 542.50 g/mol | C29H33Cl2N3O3 | 50 MG

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MPP dihydrochloride is a selective estrogen receptor (ER) modulator used in research to probe ER signaling, study agonist/antagonist effects on ERα, and induce apoptosis in estrogen-responsive cancer cell lines. It is supplied as a solid research chemical with high reported purity.

• Selective ER modulator for receptor pharmacology studies.
• Induces apoptosis in endometrial and other estrogen-responsive cell lines.
• High reported purity (≈99.5%).
• Soluble in DMSO at 30 mg/mL; ultrasonic warming may be required.
• Store sealed at 4°C; in solution keep at -80°C (6 months) or -20°C (1 month).

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