Wee1 Inhibitor II
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    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 562589

CAS#: 622855-50-9

Description: Wee1 Inhibitor II is an ATP-binding site-targeting inhibitor of Wee1.


Chemical Structure

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Wee1 Inhibitor II
CAS# 622855-50-9

Theoretical Analysis

MedKoo Cat#: 562589
Name: Wee1 Inhibitor II
CAS#: 622855-50-9
Chemical Formula: C24H19ClN2O3
Exact Mass: 418.11
Molecular Weight: 418.870
Elemental Analysis: C, 68.82; H, 4.57; Cl, 8.46; N, 6.69; O, 11.46

Price and Availability

Size Price Availability Quantity
1mg USD 385 2 Weeks
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Synonym: Wee1 Inhibitor II; Wee1 Inhibitor-II; Wee1-Inhibitor-II; Wee1-Inhibitor II;

IUPAC/Chemical Name: 6-Butyl-4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3-(2H,6H)-dione

InChi Key: HLSZACLAFZWCCS-UHFFFAOYSA-N

InChi Code: InChI=1S/C24H19ClN2O3/c1-2-3-10-27-18-9-8-13(28)11-16(18)20-19(27)12-15(14-6-4-5-7-17(14)25)21-22(20)24(30)26-23(21)29/h4-9,11-12,28H,2-3,10H2,1H3,(H,26,29,30)

SMILES Code: O=C1NC(C2=C1C3=C(C=C2C4=CC=CC=C4Cl)N(CCCC)C5=C3C=C(O)C=C5)=O

Appearance: Solid powder

Purity: >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).

Solubility: Soluble in DMSO

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: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 418.87 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.

Recalculate based on batch purity %
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
Formulation protocol:
In vitro protocol:
In vivo protocol:

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4: Maller JL, Gross SD, Schwab MS, Finkielstein CV, Taieb FE, Qian YW. Cell cycle transitions in early Xenopus development. Novartis Found Symp. 2001;237:58-73; discussion 73-8. Review. PubMed PMID: 11444050.