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萘普生(钠盐)

(S)-6-Methoxy-alpha-methyl-2-naphthaleneacetic acid sodium salt

CAS: 26159-34-2

Molecular Formula: C14H13O3.Na

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萘普生(钠盐) - Names and Identifiers

Name (S)-6-Methoxy-alpha-methyl-2-naphthaleneacetic acid sodium salt
Synonyms aleve
RS-3650
Anaprox
apranax
sodiumnaprosyn
naprosynsodium
Naproxen Sodium
Naproxen Sodium (200 mg)
sodium 2-(6-methoxynaphthalen-2-yl)propanoate
sodium (2S)-2-(6-methoxynaphthalen-2-yl)propanoate
(2S)-2-(6-Methoxy-2-naphthyl)propanoicacidsodiumsalt
6-methoxy-alpha-methyl-,sodiumsalt,(s)-2-naphthaleneaceticaci
l-(-)-6-methoxy-alpha-methyl-2-naphthaleneaceticacidsodiumsalt
6-methoxy-alpha-methyl-,sodiumsalt,l-(-)-2-naphthaleneaceticaci
[R,(-)]-6-Methoxy-α-methyl-2-naphthaleneacetic acid sodium salt
(S)-6-Methoxy-alpha-methyl-2-naphthaleneacetic acid sodium salt
6-methoxy-alpha-methyl-,sodiumsalt,l-(-)-2-naphthaleneaceticacid
CAS 26159-34-2
EINECS 247-486-2
InChI InChI=1/C14H14O3.Na/c1-9(14(15)16)10-3-4-12-8-13(17-2)6-5-11(12)7-10;/h3-9H,1-2H3,(H,15,16);/q;+1/p-1/t9-;/m0./s1

萘普生(钠盐) - Physico-chemical Properties

Molecular FormulaC14H13O3.Na
Molar Mass252.24
Melting Point250-251°C
Boling Point403.9°C at 760 mmHg
Specific Rotation(α)D -11° (in methanol)
Flash Point154.5°C
Water SolubilitySoluble in water up to 100mg/mlSoluble in methanol and chloroform. Slightly soluble in ether. Insoluble in water.
Solubility Freely soluble in water, freely soluble or soluble in methanol, sparingly soluble in ethanol (96 per cent).
Vapor Presure3.01E-07mmHg at 25°C
AppearanceWhite powder
ColorWhite to Off-White
Storage ConditionInert atmosphere,Room Temperature
UseThis product is for scientific research only and shall not be used for other purposes.
In vitro studyNaproxen acts on intact cells and inhibits COX-1 and COX-2 with an IC50 of 2.2 μg/mL and 1.3 μg/mL, respectively. In Vitro, Naproxen acts on rats and humans to reduce the production of PGE 2 and TXB 2 induced by LPS, and when PGE 2 is inhibited, the IC50 is 30.7 μm and 79.5 μm, respectively, when TXB 2 was inhibited, the IC50 was 72.4 μm and 48.3 μm, respectively. Naproxen inhibited human platelet TXB 2 Production and LPS-induced human monocyte TXB 2 production with IC50 of 5.7 and 6.4, respectively, and also slightly selectively inhibited constitutive and inducible COX-2, the ratio of the IC50 value acting on COX-1 to the IC50 value acting on COX-2 is 6.3. Only high concentration of Naproxen on HCA-7 colon cancer cells for 48 hours, can significantly induce apoptosis, IC50 is 1.45 mM.
In vivo studyIn Vivo, treatment of rats by Naproxen reduced the production of PGE 2 and TXB 2 induced by LPS with IC50 of 12.8 μm and 5.9 μm, respectively, indicating that Naproxen is a non-selective COX inhibitor. Naproxen acts on the analgesia rat model of Carrageenan-induced arthritis, IC50 is 27 μm, and on yeast-induced fever rats, IC50 is 40 μm, when PGE 2 and TXB 2 are inhibited, the IC50 was 13 μm and 5 μm, respectively.

萘普生(钠盐) - Risk and Safety

Risk CodesR22 - Harmful if swallowed
R61 - May cause harm to the unborn child
Safety DescriptionS53 - Avoid exposure - obtain special instructions before use.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
UN IDs3249
WGK Germany3
RTECSQJ1047000
HS Code2918992090
Hazard Class6.1(b)
Packing GroupIII
萘普生(钠盐)
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Tel: +86-18821248368
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View History
萘普生(钠盐)
2-Hydrazinobenzoic acid
1-Methyl-17b-hydroxy-5a-androst-1-en-3-one acetate
Isocyanic acid 3,4-dichlorophenyl ester
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