| Company Name: |
3B Pharmachem (Wuhan) International Co.,Ltd.
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| Tel: |
821-50328103-801 18930552037 |
| Email: |
3bsc@sina.com |
| Products Intro: |
Product Name:L-368,899 hydrochloride;(2S)-2-AMino-N-[(1S,2S,4R)-7,7-diMethyl-1-[[[4-(2-Methylphenyl)-1-piperazinyl]sulfonyl]Methyl]bicyclo[2.2.1]hept-2-yl]-4-(Methylsulfonyl)butanaMide
CAS:148927-60-0
Purity:99% HPLC Package:1Mg ; 5Mg;10Mg ;100Mg;250Mg ;500Mg ;1g;2.5g ;5g ;10g
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| Company Name: |
EMMX Biotechnology LLC
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| Tel: |
888-539-0666 |
| Email: |
info@emmx.com |
| Products Intro: |
Product Name:L-368,899 hydrochloride
CAS:148927-60-0
Purity:98% HPLC Package:5mg;10mg;25mg;50mg;100mg;250mg;500mg;1g
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| Company Name: |
Shanghai meikai technology co., ltd
|
| Tel: |
021-18721550-091 18721550091 |
| Email: |
yangdong@pharma.com |
| Products Intro: |
Product Name:L-368899
CAS:148927-60-0
Purity:>95% Package:5 mg|10 mg|25 mg Remarks:MC017602
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| | L-368,899hydrochloride Basic information |
| Product Name: | L-368,899hydrochloride | | Synonyms: | (2S)-2-Amino-N-[(1S,2S,4R)-7,7-dimethyl-1-[[[4-(2-methylphenyl)-1-piperazinyl]sulfonyl]methyl]bicyclo[2.2.1]hept-2-yl]-4-(methylsulfonyl)butanamide;(2S)-2-amino-N-[(1R,3S,4S)-7,7-dimethyl-4-[[4-(2-methylphenyl)piperazin-1-yl]sulfonylmethyl]-3-bicyclo[2.2.1]heptanyl]-4-methylsulfonylbutanamide;Butanamide, 2-amino-N-[(1S,2S,4R)-7,7-dimethyl-1-[[[4-(2-methylphenyl)-1-piperazinyl]sulfonyl]methyl]bicyclo[2.2.1]hept-2-yl]-4-(methylsulfonyl)-, (2S)-;L-368,899 hydrochlor;L-368899 free base | | CAS: | 148927-60-0 | | MF: | C26H42N4O5S2 | | MW: | 554.77 | | EINECS: | | | Product Categories: | | | Mol File: | 148927-60-0.mol |  |
| | L-368,899hydrochloride Chemical Properties |
| storage temp. | Store at +4°C | | solubility | Chloroform (Slightly), Methanol (Slightly), Water (Slightly) | | form | Solid | | color | Off-White to Pale Yellow | | Stability: | Hygroscopic |
| | L-368,899hydrochloride Usage And Synthesis |
| Uses | L-368,899 Dihydrochloride is an oxytoxin antagonist and may be used in the treatment of early pregnancy failure. | | Biological Activity | Potent, non-peptide and orally active oxytocin receptor antagonist (IC 50 = 8.9 nM) that displays > 40-fold selectivity over vasopressin V 1a and V 2 receptors (IC 50 values are 370 and 570 nM respectively). Antagonizes oxytocin-induced uterine contractions in vitro and in vivo . |
| | L-368,899hydrochloride Preparation Products And Raw materials |
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