WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 407186

CAS#: 1652573-86-8

Description: PLX7683 is a paradox breaker. Paradox breakers overcame several known mechanisms of resistance to first-generation RAF inhibitors. Dissociating MAPK pathway inhibition from paradoxical activation might yield both improved safety and more durable efficacy than first-generation RAF inhibitors

Chemical Structure

CAS# 1652573-86-8

Theoretical Analysis

MedKoo Cat#: 407186
Name: PLX7683
CAS#: 1652573-86-8
Chemical Formula: C23H19ClF2N4O3S
Exact Mass: 504.08345
Molecular Weight: 504.94
Elemental Analysis: C, 54.71; H, 3.79; Cl, 7.02; F, 7.53; N, 11.10; O, 9.51; S, 6.35

Size Price Shipping out time Quantity
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Pricing updated 2021-03-07. Prices are subject to change without notice.

PLX7683 is not in stock, may be available through custom synthesis. For cost-effective reason, minimum 1 gram order is requested. The product will be characterized by NMR, HPLC and MS analysis. Purity (HPLC) is usually >98%. CoA, QC data, MSDS will be provided when product is successfully made. The estimated lead time is 2-3 months. Please send email to to inquire quote.

Synonym: PLX7683; PLX-7683; PLX 7683.

IUPAC/Chemical Name: Sulfamide, N'-[4-[[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]carbonyl]-3,5-difluorophenyl]-N-ethyl-N-methyl-


InChi Code: InChI=1S/C23H19ClF2N4O3S/c1-3-30(2)34(32,33)29-16-9-19(25)21(20(26)10-16)22(31)18-12-28-23-17(18)8-14(11-27-23)13-4-6-15(24)7-5-13/h4-12,29H,3H2,1-2H3,(H,27,28)

SMILES Code: O=S(NC1=CC(F)=C(C(C2=CNC3=NC=C(C4=CC=C(Cl)C=C4)C=C32)=O)C(F)=C1)(N(CC)C)=O

Solid powder

>98% (or refer to the Certificate of Analysis)

Shipping Condition:
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition:
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Soluble in DMSO, not in water

Shelf Life:
>2 years if stored properly

Drug Formulation:
This drug may be formulated in DMSO

Stock Solution Storage:
0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code:

Handling Instructions:

Preparing Stock Solutions

The following data is based on the product molecular weight 504.94 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Select a batch to recalculate based on the batch molecular weight:
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL

Molarity Calculator

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*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and SDS / CoA (available online).

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1: Zhang C, Spevak W, Zhang Y, Burton EA, Ma Y, Habets G, Zhang J, Lin J, Ewing
T, Matusow B, Tsang G, Marimuthu A, Cho H, Wu G, Wang W, Fong D, Nguyen H, Shi S,
Womack P, Nespi M, Shellooe R, Carias H, Powell B, Light E, Sanftner L, Walters
J, Tsai J, West BL, Visor G, Rezaei H, Lin PS, Nolop K, Ibrahim PN, Hirth P,
Bollag G. RAF inhibitors that evade paradoxical MAPK pathway activation. Nature.
2015 Oct 22;526(7574):583-6. doi: 10.1038/nature14982. Epub 2015 Oct 14. PubMed
PMID: 26466569.