ChemicalBook > CAS DataBase List > BL-1249

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
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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
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
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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.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
B2186
Product name
BL-1249
Purity
≥98% (HPLC)
Packaging
10mg
Price
$261
Updated
2024/03/01
Sigma-Aldrich
Product number
B2186
Product name
BL-1249
Purity
≥98% (HPLC)
Packaging
50mg
Price
$416
Updated
2024/03/01
TRC
Product number
B595828
Product name
BL1249
Packaging
2.5mg
Price
$220
Updated
2021/12/16
ChemScene
Product number
CS-0029274
Product name
BL-1249
Purity
>99.0%
Packaging
5mg
Price
$235
Updated
2021/12/16
ApexBio Technology
Product number
B7500
Product name
BL1249
Packaging
10mg
Price
$276
Updated
2021/12/16
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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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BL-1249 Suppliers

Wuhan Shanhai Zhihe Biotechnology Co., Ltd.
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18200-13-0, BL-1249Related Search:


  • 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]-
  • 18200-13-0