Search Result

Search Result

Results for "

Vanillylamine

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Biochemical Assay Reagents (1) Isotope-Labeled Compounds (1) JNK (2)
By Research Areas:	Cancer (2)

4

Inhibitors & Agonists

1

Biochemical Assay Reagents

2

Natural
Products

1

Isotope-Labeled Compounds

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

*Vanillylamine* 1 Publications Verification	JNK	Cancer
Vanillylamine is an immediate precursor for capsaicinoids. Vanillylamine is a derivative of Vanillin (HY-N0098) is synthesized through a transaminase reaction in the phenylpropanoid pathway of capsaicinoid synthesis. Vanillylamine significantly alleviates myelosuppression caused by abdominal and pelvic tumor chemotherapy .

Vanillylamine hydrochloride 1 Publications Verification	Biochemical Assay Reagents	Others
Vanillylamine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-W097899S

Vanillylamine-d3 hydrochloride	Isotope-Labeled Compounds	Others
Vanillylamine-d₃ hydrochloride is the deuterium labeled Vanillylamine hydrochloride .

HY-W097899R

Vanillylamine (Standard)	JNK	Cancer
Vanillylamine is an immediate precursor for capsaicinoids. Vanillylamine is a derivative of Vanillin (HY-N0098) is synthesized through a transaminase reaction in the phenylpropanoid pathway of capsaicinoid synthesis. Vanillylamine significantly alleviates myelosuppression caused by abdominal and pelvic tumor chemotherapy .

Cat. No.	Product Name	Type

Vanillylamine hydrochloride 1 Publications Verification	Biochemical Assay Reagents
Vanillylamine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Cat. No.	Product Name	Category	Target	Chemical Structure

*Vanillylamine* 1 Publications Verification	Monophenols Capsicum annuum L. Classification of Application Fields Source classification Other Diseases Phenols Solanaceae Plants Disease Research Fields	JNK
Vanillylamine is an immediate precursor for capsaicinoids. Vanillylamine is a derivative of Vanillin (HY-N0098) is synthesized through a transaminase reaction in the phenylpropanoid pathway of capsaicinoid synthesis. Vanillylamine significantly alleviates myelosuppression caused by abdominal and pelvic tumor chemotherapy .

HY-W097899R

Vanillylamine (Standard)	Monophenols Capsicum annuum L. Source classification Phenols Solanaceae Plants	JNK
Vanillylamine is an immediate precursor for capsaicinoids. Vanillylamine is a derivative of Vanillin (HY-N0098) is synthesized through a transaminase reaction in the phenylpropanoid pathway of capsaicinoid synthesis. Vanillylamine significantly alleviates myelosuppression caused by abdominal and pelvic tumor chemotherapy .

Cat. No.	Product Name	Chemical Structure

HY-W097899S

Vanillylamine-d3 hydrochloride
Vanillylamine-d₃ hydrochloride is the deuterium labeled Vanillylamine hydrochloride .

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・バイオ株式会社重松貿易株式会社
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:

MedChemExpress Magic Cece

MedChemExpress: Contact Us; About Us; Headquarters; Distributors; Statement on False Report; Careers

Customer Support: Technical Support; Service; Ordering Information; Easy Return; Shipping Rates & Policies; Intellectual Property Promise

Resources: Free Sample; Resources; Molarity Calculator; Dilution Calculator; Terms & Conditions; Reconstitution Calculator; Specific Activity Calculator; DNA/RNA sequence conversion tools

Subscribe to our E-newsletter

Name
Email *

	Sorry, but the email address you supplied was invalid.

Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.

Copyright © 2013-2025 MedChemExpress. All Rights Reserved.: Site Map Privacy Policy

Join with us