1. MAPK/ERK Pathway
  2. Raf MEK
  3. Debromohymenialdisine

Debromohymenialdisine  (Synonyms: 10Z-Debromohymenialdisine)

Cat. No.: HY-113632
Handling Instructions Technical Support

Debromohymenialdisine (10Z-Debromohymenialdisine) is a pyrrole alkaloid. Debromohymenialdisine has moderate inhibitory activity with an IC50 value of 881 nM in the initial Raf/MEK-1/MAPK signaling cascade assay. Debromohymenialdisine can be used for the research of proliferation and differentiation.

For research use only. We do not sell to patients.

Debromohymenialdisine Chemical Structure

Debromohymenialdisine Chemical Structure

CAS No. : 75593-17-8

Size Stock
100 μg Get quote

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Top Publications Citing Use of Products

View All Raf Isoform Specific Products:

View All MEK Isoform Specific Products:

  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

Debromohymenialdisine (10Z-Debromohymenialdisine) is a pyrrole alkaloid. Debromohymenialdisine has moderate inhibitory activity with an IC50 value of 881 nM in the initial Raf/MEK-1/MAPK signaling cascade assay. Debromohymenialdisine can be used for the research of proliferation and differentiation[1].

IC50 & Target

IC50: 881 nM (in Raf/MEK-1/MAPK signaling cascade assay)[1].

Cellular Effect
Cell Line Type Value Description References
A498 ED50
24.7 μg/mL
Compound: 2
Cytotoxicity against human A498 cells by SRB assay
Cytotoxicity against human A498 cells by SRB assay
[PMID: 9051914]
KM-20L2 ED50
8.5 μg/mL
Compound: 2
Cytotoxicity against human KM20L2 cells by SRB assay
Cytotoxicity against human KM20L2 cells by SRB assay
[PMID: 9051914]
L5178Y EC50
1.8 μg/mL
Compound: 1d; DBH
Cytotoxicity against mouse L5178Y cells by MTT assay
Cytotoxicity against mouse L5178Y cells by MTT assay
[PMID: 33901899]
MONO-MAC-6 IC50
2.4 μg/mL
Compound: 5
Cytotoxicity against human MONO-MAC 6 cells assessed as [3H]thymidine incorporation after 48 hrs
Cytotoxicity against human MONO-MAC 6 cells assessed as [3H]thymidine incorporation after 48 hrs
[PMID: 9917317]
MONO-MAC-6 IC50
9.67 μM
Compound: 7
Cytotoxicity against human MONO-MAC-6 cells incubated for 48 hrs by [3H]-thymidine incorporation based liquid scintillation counter analysis
Cytotoxicity against human MONO-MAC-6 cells incubated for 48 hrs by [3H]-thymidine incorporation based liquid scintillation counter analysis
[PMID: 36496202]
NCI-H460 ED50
42 μg/mL
Compound: 2
Cytotoxicity against human H460 cells by SRB assay
Cytotoxicity against human H460 cells by SRB assay
[PMID: 9051914]
OVCAR-3 ED50
1.8 μg/mL
Compound: 2
Cytotoxicity against human OVCAR-3 cells by SRB assay
Cytotoxicity against human OVCAR-3 cells by SRB assay
[PMID: 9051914]
SF-295 ED50
38.9 μg/mL
Compound: 2
Cytotoxicity against human SF295 cells by SRB assay
Cytotoxicity against human SF295 cells by SRB assay
[PMID: 9051914]
SK-MEL-5 ED50
5.7 μg/mL
Compound: 2
Cytotoxicity against human SK-MEL-5 cells by SRB assay
Cytotoxicity against human SK-MEL-5 cells by SRB assay
[PMID: 9051914]
In Vitro

Debromohymenialdisine has moderate inhibitory activity with an IC50 value of 881 nM in the initial Raf/MEK-1/MAPK signaling cascade assay[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

245.24

Formula

C11H11N5O2

CAS No.
SMILES

NC(N/C1=C2CCNC(C3=C/2C=CN3)=O)=NC1=O

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass   Concentration   Volume   Molecular Weight *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Your Recently Viewed Products:

Inquiry Online

Your information is safe with us. * Required Fields.

Product Name

 

Salutation

Applicant Name *

 

Email Address *

Phone Number *

 

Organization Name *

Department *

 

Requested quantity *

Country or Region *

     

Remarks

Bulk Inquiry

Inquiry Information

Product Name:
Debromohymenialdisine
Cat. No.:
HY-113632
Quantity:
MCE Japan Authorized Agent: