BL-1249
- Product Name
- BL-1249
- CAS No.
- 18200-13-0
- Chemical Name
- BL-1249
- Synonyms
- 5,6,7,8-Tetrahydro-N-[2-(2H-tetrazol-5-yl)phenyl]-1-naphthalenamine;1-Naphthalenamine, 5,6,7,8-tetrahydro-N-[2-(2H-tetrazol-5-yl)phenyl]-
- CBNumber
- CB4503185
- Molecular Formula
- C17H17N5
- Formula Weight
- 291.35
- MOL File
- 18200-13-0.mol
BL-1249 Property
- Boiling point:
- 492.6±55.0 °C(Predicted)
- Density
- 1.291±0.06 g/cm3(Predicted)
- storage temp.
- -20°C
- solubility
- DMSO: ~17.5mg/mL
- form
- solid
- pka
- 4.10±0.10(Predicted)
- color
- pink to brown
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
H413May cause long lasting harmful effects to aquatic life
- Precautionary statements
-
P273Avoid release to the environment.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- B2186
- Product name
- BL-1249
- Purity
- ≥98% (HPLC)
- Packaging
- 10mg
- Price
- $261
- Updated
- 2024/03/01
- Product number
- B2186
- Product name
- BL-1249
- Purity
- ≥98% (HPLC)
- Packaging
- 50mg
- Price
- $416
- Updated
- 2024/03/01
- Product number
- B595828
- Product name
- BL1249
- Packaging
- 2.5mg
- Price
- $220
- Updated
- 2021/12/16
- Product number
- CS-0029274
- Product name
- BL-1249
- Purity
- >99.0%
- Packaging
- 5mg
- Price
- $235
- Updated
- 2021/12/16
- Product number
- B7500
- Product name
- BL1249
- Packaging
- 10mg
- Price
- $276
- Updated
- 2021/12/16
BL-1249 Chemical Properties,Usage,Production
Uses
BL-1249 has been used:
- as an activator of mechano-gated K2P channel in contracted mouse ileum and colon tissues
- as a TWIK related potassium channel?(TREK2) modulator and in U-2 OS osteosarcoma cell line
- as a TREK1 and TREK2 activator in mice.
General Description
BL-1249 is a non-steroid anti-inflammatory drug and an inhibitor of the cyclooxygenase (COX) enzyme.
Biological Activity
[(5, 6, 7, 8-tetrahydro-naphthalen-1-yl)-[2-(1h-tetrazol-5-yl)-phenyl]-amine], named bl 1249, is a putative potassium channel opener with bladder-relaxant properties. in cultured bladder smooth muscle cells, bl 1249 decreased dibac4 (3) fluorescence in a concentration-dependent manner with an ec50 of 1.26 ± 0.6 μm. in human bladder cells, bl 1249 resulted in hyperpolarization in a concentration-dependent manner and yielded an ec50 of 1.49±0.08 μm. bl 1249 relaxed 30 mm kcl precontracted bladder strips in a concentration-dependent manner and yielded an ec50 of 1.1 ± 0.37 μm [1].there are several types of potassium channels in urinary bladder myocytes and they are important in determining contractility and excitability of bladder smooth muscle. these channels include maxi-k+, katp, members of the voltage-gated kv family, sk family and, possibly, members of the kcnq family. open potassium channels can increase potassium efflux from the cell and produce membrane potential hyperpolarization, thereby decrease the activation of voltage-dependent calcium channels [1].in human bladder myocytes, bl 1249 produced large instantaneously non-inactivating, activating outward currents that were readily reversible following drug washout. the bl 1249-induced current was hence of a reversal potential of near -80 mv under the physiological k+ gradient, this indicated that the current is carried by k+ ions [1].in anesthetized rats, bl 1249 at a concentration of 1 mg/kg significantly decreased (p< 0.01) micturition contractions during the 15-min period immediately following dosing; for the 15- to 30-min period, the decrease was significant but less (p< 0.05). administration of bl 1249 at a concentration of 1 mg/kg had no effect on mean arterial blood pressure (mabp) during the 0- to 15-min period immediately following administration. during the 15- to 30-min period, bl 1249 administration increased mabp by less than 10% [1].
Biochem/physiol Actions
BL-1249 also activates TWIK related potassium channel 2?(TREK2). It interacts with K2P channel at the negatively charged activator site and modulates channel opening.
storage
Store at -20°C
References
[1]. svetlana tertyshnikova, ronald j. knox, mary jane plym, et al. bl-1249 [(5, 6, 7, 8-tetrahydro-naphthalen-1-yl)-[2-(1h-tetrazol-5-yl)-phenyl]-amine]: a putative potassium channel opener with bladder-relaxant properties. the journal of pharmacology and experimental therapeutics, 2015, 313(1):250-259.
BL-1249 Preparation Products And Raw materials
Raw materials
Preparation Products
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