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ML141

SKU: orb1224170

Description

ML141 is a potent, selective and reversible non-competitive inhibitor of Rho family GTPase cdc42 with IC50 of 200 nM.

Images & Validation

Key Properties

CAS Number71203-35-5
MW407.49
Purity>98% (HPLC)
FormulaC22H21N3O3S
SMILESO=S(C1=CC=C(N2N=C(C3=CC=CC=C3)CC2C4=CC=C(OC)C=C4)C=C1)(N)=O
TargetCDK
SolubilityDMSO: 81 mg/mL warmed (198.77 mM)

Bioactivity

In Vivo
ML141 (CID-2950007) (10 μM; intracerebroventricular injection) causes acute anxiety in mice. Animal model: C57Bl/6J mice. Dosage: 10 μM. Administration: Intracerebroventricular injection. Result: Increased anxiety in mice.
In Vitro
ML141 (CID-2950007) is not cytotoxic in either cell line at doses of 0.1-3 μM after treatment for 4 days. OVCA429 cells were insensitive to 10 μM compound, whereas some cytotoxicity was observed in SKOV3ip cells at this concentration after a 4-day treatment, although it did not reach statistical significance. ML141 is not cytotoxic toward Swiss 3T3 or Vero E6 cells up to 10 μM for 24 and 48 h, respectively. ML141 inhibits 3T3 fibroblast filopodia formation and inhibits ovarian cancer cell migration.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

CID2950007

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  • ML141 [orb1305451]

    99.36% (May vary between batches)

    71203-35-5

    407.49

    C22H21N3O3S

    50 mg, 2 mg, 5 mg, 25 mg, 1 mg, 1 ml x 10 mM (in DMSO), 10 mg, 100 mg
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Protocol Information

Available Sizes

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2 mg
$ 90.00
5 mg
$ 120.00
10 mg
$ 190.00
25 mg
$ 380.00
50 mg
$ 670.00
100 mg
$ 950.00
500 mg
$ 2,030.00