Search Result

Results for "

piperidine

" in MedChemExpress (MCE) Product Catalog:

By Targets:	5-HT Receptor (4) ADC Linker (4) Adrenergic Receptor (1) Amino Acid Derivatives (1) Androgen Receptor (1) Apoptosis (3) Autophagy (18) Bacterial (2) Biochemical Assay Reagents (8) Btk (2) CD38 (1) DNA/RNA Synthesis (2) Drug Derivative (5) Drug Intermediate (2) Drug Metabolite (1) E3 Ligase Ligand-Linker Conjugates (24) Endogenous Metabolite (2) Epigenetic Reader Domain (1) Epoxide Hydrolase (1) Estrogen Receptor/ERR (1) Fungal (2) GABA Receptor (1) GHSR (2) Glycosidase (1) Histone Demethylase (3) iGluR (1) Isotope-Labeled Compounds (6) Itk (1) Ligands for E3 Ligase (28) Ligands for Target Protein for PROTAC (4) mAChR (5) Melanocortin Receptor (1) Mitochondrial Metabolism (2) Monoamine Oxidase (1) nAChR (2) Neuropeptide FF Receptor (1) Opioid Receptor (3) PARP (2) Phosphodiesterase (PDE) (1) Potassium Channel (3) PPAR (1) PROTAC Linkers (16) PROTACs (5) Ras (1) Reactive Oxygen Species (2) Reference Standards (3) Target Protein Ligand-Linker Conjugates (3) Tyrosinase (1)
By Research Areas:	Cancer (95) Cardiovascular Disease (5) Endocrinology (2) Infection (5) Inflammation/Immunology (4) Metabolic Disease (2) Neurological Disease (23)
Click Chemistry:	PROTAC Synthesis (1)

147

Inhibitors & Agonists

Biochemical Assay Reagents

Peptides

Natural
Products

Isotope-Labeled Compounds

Click Chemistry

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-139116

Piperidine-4-sulfonic acid	GABA Receptor	Neurological Disease
Piperidine-4-sulfonic acid is a potent GABA agonist with an IC₅₀ of 0.034 μM for the inhibition of the binding of H-GABA .

HY-134592

Piperidine-GNE-049-N-Boc	Ligands for Target Protein for PROTAC	Cancer
Piperidine-GNE-049-N-Boc is a ligand for target protein for PROTAC of dCBP-1 (HY-134582). dCBP-1 is a potent and selective heterobifunctional degrader of p300/CBP .

HY-W687952

Piperidine-C-piperidine-Boc	PROTAC Linkers	Others
Piperidine-C-piperidine-Boc is a PROTAC linker. Piperidine-C-piperidine-Boc is the linker of CDK2 degrader 2 (HY-163815) .

HY-W012935

Piperidine-4-carbaldehyde piperidine-4-carboxaldehyde	PROTAC Linkers	Cancer
Piperidine-4-carbaldehyde (Piperidine-4-carboxaldehyde) is a PROTAC Linker. Piperidine-4-carbaldehyde can be used to optimize combined with the target protein affinity, thus improve the PROTAC the molecular degradation efficiency. Piperidine-4-carbaldehyde can be used in the CDK2 PROTACs (HY-161708) .

HY-W012748S

Piperidine-4-carboxamide-d9	Isotope-Labeled Compounds	Others
Piperidine-4-carboxamide-d₉ is the deuterium labeled Piperidine-4-carboxamide .

HY-168388

Piperidine-C2-piperazine-Boc	PROTAC Linkers	Cancer
Piperidine-C2-piperazine-Boc is a PROTAC linker that can be used in the synthesis of PROTACs .

HY-168297

Piperidine-C2-Pip-C-COOH	PROTAC Linkers	Cancer
Piperidine-C2-Pip-C-COOH is a linker for PROTAC BTK Degrader-5 (HY-155072), significantly improving metabolic stability, and can be used in cancer research .

HY-168723

Piperidine-C-Pip-C2-Pip-C2-OH	PROTAC Linkers	Cancer
Piperidine-C-Pip-C2-Pip-C2-OH is a PROTAC Linker that can be used to synthesize the PROTAC PARP1 degrader-3 (HY-168722) for tumor research .

HY-W584986

Thalidomide-(2)piperidine	Ligands for E3 Ligase	Cancer
Thalidomide-(2)piperidine (compound 9) is a potent E3 ligase ligand. Thalidomide-(2)piperidine can be used for synthesis of PROTACs .

HY-161202

*Thalidomide-piperidine-O-piperidine-C2-OH*	Ligands for E3 Ligase Autophagy	Cancer
Thalidomide-piperidine-O-piperidine-C2-OH is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Thalidomide-piperidine-O-piperidine-C2-OH can serve as a Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

HY-169050

Thalidomide-piperidine	E3 Ligase Ligand-Linker Conjugates	Cancer
Thalidomide-piperidine is an E3 Ligase Ligand-Linker Conjugate. Thalidomide-piperidine can be used to synthesize SMART1 (HY-W998345) .

HY-138783A

*Thalidomide-Piperazine-Piperidine* hydrochloride**	E3 Ligase Ligand-Linker Conjugates	Cancer
Thalidomide-Piperazine-Piperidine hydrochloride is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-Piperazine-Piperidine hydrochloride incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology .

HY-125828

1-(3,4-Dimethoxycinnamoyl)piperidine	Bacterial	Infection
1-(3,4-Dimethoxycinnamoyl)piperidine, a synthesized piperidine analog, possesses antimicrobial and antioxidant activity .

HY-33540S

*1-(Chlorocarbonyl)piperidine-d10*	Isotope-Labeled Compounds	Others
1-(Chlorocarbonyl)piperidine-d₁₀ is the deuterium labeled 1-(Chlorocarbonyl)piperidine .

HY-P2336A

CCZ01048 TFA 2 Publications Verification	Melanocortin Receptor	Cancer
CCZ01048 TFA, a α-MSH analogue, exhibits high binding affinity to melanocortin 1 receptor (MC1R) with a K_i of 0.31 nM. CCZ01048 TFA shows rapid internalization into B16F10 melanoma cells and high in vivo stability. CCZ01048 TFA is a promising candidate for PET imaging of malignant melanoma .

HY-130983

*N-piperidine* Ibrutinib hydrochloride**	Btk Ligands for Target Protein for PROTAC	Cancer
N-piperidine Ibrutinib hydrochloride (Compound 1) is a reversible Ibrutinib derivative. N-piperidine Ibrutinib hydrochloride is a potent BTK inhibitor with IC₅₀s of 51.0 and 30.7 nM for WT BTK and C481S BTK, respectively . N-piperidine Ibrutinib hydrochloride can be used as a BTK ligand in the synthesis of a series of PROTACs, such as SJF620 (HY-133137). SJF620 is a potent PROTAC BTK degrader with a DC₅₀ of 7.9 nM .

HY-176187

DDR1 ligand 1-piperidine	Target Protein Ligand-Linker Conjugates	Cancer
DDR1 ligand 1-piperidine is a target protein ligand and linker conjugate, which can be used for the synthesis of PROTAC DDR1 degrader-1 (HY-176184) .

HY-163237

*Thalidomide-piperidine-O-azetidineethanol*	Ligands for E3 Ligase Autophagy	Cancer
Thalidomide-piperidine-O-azetidineethanol is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Thalidomide-piperidine-O-azetidineethanol can serve as a Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

HY-163232

*Phthalimidinoglutarimide-piperidine-NH-Boc*	E3 Ligase Ligand-Linker Conjugates	Cancer
Phthalimidinoglutarimide-piperidine-NH-Boc is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Phthalimidinoglutarimide-piperidine-NH-Boc can serve as a Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

HY-163234

*Phthalimidinoglutarimide-piperidine-NH2*	E3 Ligase Ligand-Linker Conjugates	Cancer
Phthalimidinoglutarimide-piperidine-NH2 is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Phthalimidinoglutarimide-piperidine-NH2 can serve as a Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

HY-150666S

1-(3,4-Dimethoxy-d6-benzoyl)piperidine	Isotope-Labeled Compounds	Others
1-(3,4- Dimethoxy-d₆-benzoyl) piperidine is the deuterium labeled 1-(3,4- Dimethoxy-benzoyl) piperidine .

HY-121964

*cis-Piperidine-2,3-dicarboxylic acid*	iGluR	Neurological Disease
Cis-piperidine-2,3-dicarboxylic acid is a non-specific antagonist of NMDA, AMPA and kainate ionotropic receptors and a partial agonist for NMDA receptors. Cis-piperidine-2,3-dicarboxylic acid can be used in blocking general excitatory synaptic transmissions .

HY-168203

*Thalidomide-piperidine-O-Ph-NH2*	E3 Ligase Ligand-Linker Conjugates	Cancer
Thalidomide-piperidine-O-Ph-NH2 is the conjugate of E3 ligase and linker. Thalidomide-piperidine-O-Ph-NH2 can be used for synthesis of PROTAC degrader MJP6412 (HY-168201) .

HY-W904851

*Boc-Piperidine-piperazine-Cbz*	PROTAC Linkers	Cancer
Boc-Piperidine-piperazine-Cbz is a PROTAC linker that can be used in the synthesis of ZLC491 (HY-168162) .

HY-168039

*Boc-NH-Piperidine-C5-OH*	PROTAC Linkers	Cancer
Boc-NH-Piperidine-C5-OH is a PROTAC linker. Boc-NH-Piperidine-C5-OH can be used in the synthesis of PROTAC PIN1 degrader-1 (HY-168037) .

HY-163236

*Thalidomide-piperidine-O-azetidine-acetic acid*	Ligands for E3 Ligase Autophagy	Cancer
Thalidomide-piperidine-O-azetidine-acetic acid is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Thalidomide-piperidine-O-azetidine-acetic acid can serve as a Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

HY-138783

Thalidomide-Piperazine-Piperidine	E3 Ligase Ligand-Linker Conjugates Autophagy Apoptosis	Cancer
Thalidomide-Piperazine-Piperidine is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology .

HY-163922

*CRBN ligand-1-piperidine-Me*	E3 Ligase Ligand-Linker Conjugates	Cancer
CRBN ligand-1-piperidine-Me is an E3 ligase ligand-linker conjugate.

HY-168217

*Thalidomide-piperazine-piperidine-2-F-Ph-CHO*	E3 Ligase Ligand-Linker Conjugates	Cancer
Thalidomide-piperazine-piperidine-2-F-Ph-CHO is a E3 ligase ligand-linker conjugate, which is consisted of a Thalidomide (HY-14658) and a linker Boc-Piperazine-piperidine-2-F-Ph-CHO (HY-168218). Thalidomide-piperazine-piperidine-2-F-Ph-CHO is utilized for synthesis of PROTAC molecule YDR1 (HY-168215) .

HY-176137

*7-Azaspiro[3.5]nonane-piperidine-Boc*	PROTAC Linkers	Cancer
7-Azaspiro[3.5]nonane-piperidine-Boc is a PROTAC linker. 7-Azaspiro[3.5]nonane-piperidine-Boc can be used to synthesize RP03707 (HY-176134) .

HY-168389

*Thalidomide-piperidine-C2-piperazine-Boc*	E3 Ligase Ligand-Linker Conjugates	Cancer
Thalidomide-piperidine-C2-piperazine-Boc is an E3 ligase ligand-linker conjugate that incorporates the Thalidomide (HY-130639) based cereblon ligand and a linker used in PROTAC technology. Thalidomide-piperidine-C2-piperazine-Boc can be used for synthesis of PROTACs .

HY-168272

(3S)Lenalidomide-piperazine-C-piperidine	E3 Ligase Ligand-Linker Conjugates	Cancer
(3S)Lenalidomide-piperazine-C-piperidine is an E3 ubiquitinase ligand + linker conjugate (E3 Ligase Ligand-Linker Conjugates). (3S)Lenalidomide-piperazine-C-piperidine can be used to synthesize PROTAC PROTAC ER Degrader-11 (HY-168270) .

HY-168231

*trans-Boc-Piperidine-C-PIP-O-cyclobutane-OH*	PROTAC Linkers	Cancer
trans-Boc-Piperidine-C-PIP-O-cyclobutane-OH is a PROTAC linker. trans-Boc-Piperidine-C-PIP-O-cyclobutane-OH can be used to synthesize PROTAC SMARCA2 degrader-27 (HY-168229) .

HY-168040

*Thalidomide-O-C5-piperidine-NH-Boc*	E3 Ligase Ligand-Linker Conjugates	Cancer
Thalidomide-O-C5-piperidine-NH-Boc is an E3 Ligase Ligand-Linker Conjugate. Thalidomide-O-C5-piperidine-NH-Boc can be used to synthesize PROTAC PIN1 degrader-1 (HY-168037) .

HY-135670A

β-glycosidase-IN-1	Glycosidase	Metabolic Disease
β-glycosidase-IN-1 (Compound 33) is a piperidine derivative and a β-glycosidase inhibitor. β-glycosidase-IN-1 has hypoglycemic activity .

HY-161185

*Thalidomide-piperidine-O-azetidine-boc*	Ligands for E3 Ligase	Cancer
Thalidomide-piperidine-O-azetidine-boc is a conjugate of E3 ubiquitin ligase ligand-Linker, which can be used to synthesize complete PROTACs molecules.

HY-169489

*2F-Pyrimidine-piperidine-spiro[3.3]heptane-acid*	PROTAC Linkers	Cancer
2F-Pyrimidine-piperidine-spiro[3.3]heptane-acid is a PROTAC linker. 2F-Pyrimidine-piperidine-spiro[3.3]heptane-acid can be used in the synthesis of PROTACs (e.g. HY-169272) .

HY-W200249

Meta-methyl 4-anilino-1-Boc-piperidine	Drug Derivative	Neurological Disease
Meta-methyl 4-anilino-1-Boc-piperidine is a precursor in the synthesis of a compound.

HY-150341

Ortho-methyl 4-anilino-1-boc-piperidine	Opioid Receptor	Neurological Disease
Ortho-methyl 4-anilino-1-boc-piperidine is a precursor in the synthesis of a compound.

HY-W399538

Para-methyl 4-anilino-1-boc-piperidine	Drug Derivative	Neurological Disease
Para-methyl 4-anilino-1-boc-piperidine is a precursor in the synthesis of a compound.

HY-161198

*Thalidomide-azetidine-pyrrolidine-C-piperidine-C-boc*	Ligands for E3 Ligase Autophagy	Cancer
Thalidomide-azetidine-pyrrolidine-C-piperidine-C-boc is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Thalidomide-azetidine-pyrrolidine-C-piperidine-C-boc can serve as a Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

HY-161195

*Deoxy-thalidomide-piperidine-C-piperazine-C-boc*	Ligands for E3 Ligase Autophagy	Cancer
Deoxy-thalidomide-piperidine-C-piperazine-C-boc is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Deoxy-thalidomide-piperidine-C-piperazine-C-boc can serve as a Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

HY-40007

1-Boc-4-(aminomethyl)piperidine	Biochemical Assay Reagents	Others
1-Boc-4-(aminomethyl)piperidine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-168197

*Thalidomide-F-piperidine-piperazine-Cbz*	PROTACs	Cancer
Thalidomide-F-piperidine-piperazine-Cbz Conjugate 110 is a conjugate of E3 ligase and linker for the synthesis of CDK12/13 PROTAC degrader (HY-168162) .

HY-N3526

Calyxamine B	Others	Others
Calyxamine B is a piperidine alkaloid that can be isolated from Calyx podatypa .

HY-168227

*trans-Boronic acid pinacol-pyrazole-C-cyclobutane-O-piperidine-Boc*	PROTAC Linkers	Cancer
trans-Boronic acid pinacol-pyrazole-C-cyclobutane-O-piperidine-Boc is a PROTAC linker. trans-Boronic acid pinacol-pyrazole-C-cyclobutane-O-piperidine-Boc can be used in the synthesis of PROTAC SMARCA2/4-degrader-35 (HY-168225) .

HY-172625

*VH 101-amide-piperidine-Pip-alkyne*	E3 Ligase Ligand-Linker Conjugates	Cancer
VH 101-amide-piperidine-Pip-alkyne is an E3 Ligase Ligand-Linker Conjugates that can be used to synthesize PROTAC degrader. The linker part of VH 101-amide-piperidine-Pip-alkyne is tert-Butyl 4-ethynyl-[1,4'-bipiperidine]-1'-carboxylate (HY-W442074), and the VHL-type E3 ubiquitinase ligand is VH 101, acid (HY-47070) .

HY-168239

*Thalidomide-piperidine-CO-piperazine-C-3-Br-Ph*	E3 Ligase Ligand-Linker Conjugates	Cancer
Thalidomide-piperidine-CO-piperazine-C-3-Br-Ph is an E3 ligase ligand-linker conjugate (E3 Ligase Ligand-Linker Conjugates). Thalidomide-piperidine-CO-piperazine-C-3-Br-Ph can be used for the synthesis of PROTAC SMARCA2 degrader-28 (HY-168236) .

HY-161199

*Thalidomide-azetidine-pyrrolidine-C-piperidine-C2-OH*	Ligands for E3 Ligase Autophagy	Cancer
Thalidomide-azetidine-pyrrolidine-C-piperidine-C2-OH is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Thalidomide-azetidine-pyrrolidine-C-piperidine-C2-OH can serve as Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

HY-161184

*Deoxy-thalidomide-piperidine-C-piperazine-C2-OH*	Ligands for E3 Ligase Autophagy	Cancer
Deoxy-thalidomide-piperidine-C-piperazine-C2-OH is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Deoxy-thalidomide-piperidine-C-piperazine-C2-OH can serve as a Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

Cat. No.	Product Name	Target	Research Area

HY-P2336A

CCZ01048 TFA 2 Publications Verification	Melanocortin Receptor	Cancer
CCZ01048 TFA, a α-MSH analogue, exhibits high binding affinity to melanocortin 1 receptor (MC1R) with a K_i of 0.31 nM. CCZ01048 TFA shows rapid internalization into B16F10 melanoma cells and high in vivo stability. CCZ01048 TFA is a promising candidate for PET imaging of malignant melanoma .

HY-43459

*(4-(Thiazol-2-ylcarbamoyl)piperidine-1-carbonyl)-L-leucine*	Amino Acid Derivatives	Others
(4-(Thiazol-2-ylcarbamoyl)piperidine-1-carbonyl)-L-leucine is a leucine derivative .

HY-P10563

Noraramtide BHV-1100	CD38	Cancer
Noraramtide (BHV-1100) is an antibody recruitment molecule. Noraramtide can specifically bind to CD38 molecules to recruit natural killer (NK) cells. Noraramtide enhances the ability of NK cells to kill tumor cells through antibody-dependent cellular cytotoxicity (ADCC). This mechanism allows NK cells to more effectively recognize and eliminate tumor cells while avoiding mutual killing between NK cells. Noraramtide can be used for the study of autologous cancer immunity .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-N3526

Calyxamine B	Structural Classification Alkaloids Piperidine Alkaloids Source classification Marine natural products Sponge	Others
Calyxamine B is a piperidine alkaloid that can be isolated from Calyx podatypa .

HY-114791

Lobelanidine	Structural Classification Alkaloids Lobelia tupa L. Other Alkaloids Source classification Campanulaceae Plants	nAChR
Lobelanidine is an antagonist for nicotinic acetylcholine receptor (nAChR), which inhibits α7 nAChR response and α3β2/α3β4 nAChR responses, with IC₅₀ of 2.8 and 8.2 μM .

HY-121229A

(±)-Coniine 2-Propylpiperidine	Alkaloids Piperidine Alkaloids Structural Classification Tsuga chinensis (Franch.) Pritz. Classification of Application Fields Pinaceae Source classification Other Diseases Plants Disease Research Fields	nAChR
(±)-Coniine (2-Propylpiperidine) is a piperidine alkaloid and nAChR agonist (EC₅₀=0.3 mM). (±)-Coniine is acutely toxic to mice with an LD50 value of 7.7 mg/kg .

Cat. No.	Product Name	Chemical Structure

HY-W012748S

Piperidine-4-carboxamide-d9
Piperidine-4-carboxamide-d₉ is the deuterium labeled Piperidine-4-carboxamide .

HY-33540S

*1-(Chlorocarbonyl)piperidine-d10*
1-(Chlorocarbonyl)piperidine-d₁₀ is the deuterium labeled 1-(Chlorocarbonyl)piperidine .

HY-150666S

1-(3,4-Dimethoxy-d6-benzoyl)piperidine
1-(3,4- Dimethoxy-d₆-benzoyl) piperidine is the deuterium labeled 1-(3,4- Dimethoxy-benzoyl) piperidine .

HY-12760S

Indoramin-d5
Indoramin-d₅ is deuterium labeled Indoramin, which is a piperidine antiadrenergic agent.

HY-W697671S

Paroxetine-d6 hydrochloride
Paroxetine-d₆ (hydrochloride) is deuterium labeled trans-3-((Benzo[d][1,3]dioxol-5-yloxy)methyl)-4-(4-fluorophenyl)piperidine hydrochloride .

HY-Z1430S

(3R,4S)-Paroxetine-d4 hydrochloride
Paroxetine EP impurity D-d₄ (hydrochloride) is deuterium labeled (3R,4S)-3-((benzo[d][1,3]dioxol-5-yloxy)methyl)-4-(4-fluorophenyl)piperidine (Paroxetine Impurity).

Cat. No.	Product Name		Classification

HY-114402

ARD-69		PROTAC Synthesis
ARD-69 is a PROTAC degrader based on the E3 ubiquitin ligase VHL and targeting the androgen receptor, which can induce androgen receptor (AR) protein degradation in AR-positive prostate cancer cells. ARD-69 inhibits AR-regulated gene expression, binds to the AR ligand binding domain at one end and binds to VHL at the other end, prompting AR to be recruited to the E3 ubiquitin ligase complex, triggering proteasome degradation, thereby inhibiting AR signaling pathways and downstream gene expression (such as PSA, TMPRSS2). ARD-69 can be used to study the treatment of castration-resistant prostate cancer (mCRPC) . ARD-69 is composed of a target protein ligand (pink part) AR antagonist 14 (HY-172624), a PROTAC linker (black part) tert-Butyl 4-ethynyl-[1,4'-bipiperidine]-1'-carboxylate (HY-W442074), and a VHL-type E3 ubiquitinase ligand (blue part) VH 101, acid (HY-47070); among them, the VHL ligand and the linker can form a conjugate VH 101-amide-piperidine-Pip-alkyne (HY-172625).

Inquiry Online

Your information is safe with us. * Required Fields.

MCE Japan Authorized Agent ナミキ商事株式会社コスモ・バイオ株式会社
Salutation			Country or Region *
Applicant Name *			Organization Name *
Department *
Email Address *			Product Name *
Cat. No.			Requested quantity *
Phone Number *
Remarks

Inquiry Online

Inquiry Information

Product Name:
Cat. No.:
Quantity:
MCE Japan Authorized Agent:

piperidine

Inhibitors & Agonists

Biochemical Assay Reagents

Peptides

NaturalProducts

Isotope-Labeled Compounds

Click Chemistry

Natural
Products