ML-7 HYDROCHLORIDE
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- ₹16302.45 - ₹17860
- Product name: ML-7 HYDROCHLORIDE
- CAS: 110448-33-4
- MF: C15H18ClIN2O2S
- MW: 452.74
- EINECS:
- MDL Number:MFCD00065524
- Synonyms:1-(5-IODONAPHTHALENE-1-SULFONYL)-1H-HEXAHYDRO-1,4-DIAZEPINE HCL;1-(5-IODONAPHTHALENE-1-SULFONYL)-1H-HEXAHYDRO-1,4-DIAZEPINE HYDROCHLORIDE;1-(5-IODONAPHTHALENE-1-SULFONYL)HOMOPIPERAZINE, HCL;1-(5-IODONAPHTHALENE-1-SULFONYL)-1H-HEXAHYDRO-1,4-DIAZEPINE;1-(5-iodonaphthalene-1-sulfonyl)-1H-*hexahydro-1,;ML-7, HCl;1-(5-IODONAPHTHALENE-1-SULFONYL)-1H-*HEX AHYDRO-1,4-;1-(5-Iodonaphthalene-1-sulfonyl)-1H-hexahydro-1,4-diazepine, hyd
2 prices
Selected condition：
Brand
- Sigma-Aldrich(India)
Package
- 1MG
- 5MG
- ManufacturerSigma-Aldrich(India)
- Product number475880
- Product descriptionML-7, Hydrochloride - CAS 110448-33-4 - Calbiochem A cell-permeable, potent, reversible, ATP-competitive, and selective inhibitor of myosin light chain kinase (Ki = 300 nM).
- Packaging1MG
- Price₹17860
- Updated2022-06-14
- Buy
- ManufacturerSigma-Aldrich(India)
- Product numberI2764
- Product descriptionML-7 powder
- Packaging5MG
- Price₹16302.45
- Updated2022-06-14
- Buy
| Manufacturer | Product number | Product description | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|
| Sigma-Aldrich(India) | 475880 | ML-7, Hydrochloride - CAS 110448-33-4 - Calbiochem A cell-permeable, potent, reversible, ATP-competitive, and selective inhibitor of myosin light chain kinase (Ki = 300 nM). | 1MG | ₹17860 | 2022-06-14 | Buy |
| Sigma-Aldrich(India) | I2764 | ML-7 powder | 5MG | ₹16302.45 | 2022-06-14 | Buy |
Properties
Melting point :246-249°C dec.
storage temp. :-20°C
solubility :insoluble in EtOH; ≥15.95 mg/mL in DMSO; ≥8.82 mg/mL in H2O with gentle warming and ultrasonic
form :powder
color :white
storage temp. :-20°C
solubility :insoluble in EtOH; ≥15.95 mg/mL in DMSO; ≥8.82 mg/mL in H2O with gentle warming and ultrasonic
form :powder
color :white
Safety Information
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Description
ML-7 inhibits smooth muscle myosin light chain kinase (MLCK) with a Ki value of 0.3 μM and displays reversible, ATP-competitive inhibition of Ca2+-calmodulin-dependent and -independent smooth muscle MLCKs. It exhibits a 10-fold more potent inhibition of MLCK than its parent compound ML-9 .More related product prices
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