An inhibitor of P-glycoprotein
Technical Support & Resources

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

HM30181

Item No. 32873

Technical Information
Formal Name
N-[2-[2-[4-[2-(3,4-dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)ethyl]phenyl]-2H-tetrazol-5-yl]-4,5-dimethoxyphenyl]-4-oxo-4H-1-benzopyran-2-carboxamide
CAS Number
849675-66-7
Synonyms
  • Encequidar
Molecular Formula
C38H36N6O7
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/ml
SMILES
COC(C=C1C2=NN(C3=CC=C(CCN4CC(C=C(OC)C(OC)=C5)=C5CC4)C=C3)N=N2)=C(C=C1NC(C6=CC(C7=C(O6)C=CC=C7)=O)=O)OC
InChi Code
InChI=1S/C38H36N6O7/c1-47-32-17-24-14-16-43(22-25(24)18-33(32)48-2)15-13-23-9-11-26(12-10-23)44-41-37(40-42-44)28-19-34(49-3)35(50-4)20-29(28)39-38(46)36-21-30(45)27-7-5-6-8-31(27)51-36/h5-12,17-21H,13-16,22H2,1-4H3,(H,39,46)
InChi Key
AHJUHHDDCJQACA-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Add

    Cayman Chemical
    Visit Our Cancer Resource Center
    Find Tools & Resources to Study the Hallmarks of Cancer
    • Cancer cell signaling & regulation
    • Cancer metabolism
    • Tumor microenvironment
    EXPLORE NOW
    Product Description

    HM30181 is an inhibitor of P-glycoprotein (P-gp), also known as multidrug resistance protein 1 (MDR1; IC50 = 0.63 nM).1 It is selective for P-gp over breast cancer resistance protein (BCRP; IC50 = 3,700 nM), as well as multidrug resistance-associated protein 1 (MRP1), MRP2, and MRP3 at 100 µM. It inhibits transepithelial basal-to-apical transport of paclitaxel in MDCK monolayers overexpressing P-gp (IC50 = 35.4 nM). HM30181 inhibits tumor growth and induces tumor regression in an HT-29 mouse xenograft model when administered at doses of 10 and 20 mg/kg, respectively, in combination with paclitaxel (Item No. 10461).

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Kwak, J.-O., Lee, S.H., Lee, G.S., et alSelective inhibition of MDR1 (ABCB1) by HM30181 increases oral bioavailability and therapeutic efficacy of paclitaxel. Eur. J. Pharmacol. 627(1-3), 92-98 (2009).