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Lornoxicam

CAS No.
70374-39-9
Chemical Name:
Lornoxicam
Synonyms
Lornoxicam Impurity 33;6-Chloro-4-hydroxy-2-methyl-N-pyridin-2-yl-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide 1,1-dioxide (Lornoxicam);Xefo;Telos;TS 110;Xefocam;ornoxicam;AKOS 93662;LORNOXICAM;Ro 13-9297
CBNumber:
CB7224647
Molecular Formula:
C13H10ClN3O4S2
Molecular Weight:
371.82
MDL Number:
MFCD00866163
MOL File:
70374-39-9.mol
Last updated:2023-12-22 17:53:22

Lornoxicam Properties

Melting point 225-230°C (dec.)
Density 1.742±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility DMSO: >5mg/mL (warmed)
pka pKa2 4.7(at 25℃)
form powder
color faint yellow to dark yellow
Merck 14,5582
InChIKey WLHQHAUOOXYABV-UHFFFAOYSA-N
CAS DataBase Reference 70374-39-9(CAS DataBase Reference)
FDA UNII ER09126G7A
ATC code M01AC05

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H300
Precautionary statements  P264-P301+P310
Hazard Codes  Xi,T+
Risk Statements  36/37/38-28
Safety Statements  26-36-45-36/37-28
RIDADR  UN 2811 6.1 / PGII
WGK Germany  3
RTECS  XJ9095000
HazardClass  IRRITANT
PackingGroup  II
HS Code  29349990
Toxicity LD50 orally in mice, rats, rabbits, dogs, monkeys: >10 mg/kg (Pruss)
NFPA 704
0
4 0

Lornoxicam price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML0338 Lornoxicam ≥98% (HPLC) 70374-39-9 10mg $96.7 2024-03-01 Buy
Sigma-Aldrich SML0338 Lornoxicam ≥98% (HPLC) 70374-39-9 50mg $314 2024-03-01 Buy
TCI Chemical L0239 Lornoxicam >98.0%(HPLC)(N) 70374-39-9 1g $135 2024-03-01 Buy
TCI Chemical L0239 Lornoxicam >98.0%(HPLC)(N) 70374-39-9 5g $404 2024-03-01 Buy
Cayman Chemical 70220 Lornoxicam ≥98% 70374-39-9 50mg $57 2024-03-01 Buy
Product number Packaging Price Buy
SML0338 10mg $96.7 Buy
SML0338 50mg $314 Buy
L0239 1g $135 Buy
L0239 5g $404 Buy
70220 50mg $57 Buy

Lornoxicam Chemical Properties,Uses,Production

Description

Lornoxicam (Trade name: “Xefo”) belongs to a non-steroidal anti-inflammatory drug. As a kind of oxicam class drug, it has analgesic, anti-inflammatory and antipyretic properties. It can be used for the treatment of various type of acute mild to moderate pain which results from inflammatory diseases of the joints, osteoarthritis, surgery, sciatica and rheumatic diseases. Lornoxicam is capable of potently inhibiting the prostaglandin biosynthesis process, making it have highly pronounced efficacy. The exact mechanism of Lornoxicam is not exactly understood. However, it is indicated that Lornoxicam can inhibit the prostaglandin and thromboxane synthesis by inhibiting both COX-1 and COX-2, leading to reduction of inflammation, pain, fever, and swelling.

References

https://www.drugbank.ca/drugs/DB06725
https://en.wikipedia.org/wiki/Lornoxicam

Description

Lornoxicam is a COX inhibitor and non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory and analgesic properties. It inhibits production of thromboxane B2 (TXB2; ) from arachidonic acid (Item Nos. 90010 | 90010.1 | 10006607) in HEL human erythroleukemic cells (IC50 = 3 nM), which endogenously express COX-1, as well as inhibits LPS-induced formation of prostaglandin F (PGF; ) from arachidonic acid in Mono-Mac-6 cells (IC50 = 8 nM), which endogenously express COX-2. Lornoxicam reduces LPS-induced production of nitric oxide and IL-6 in cell-based assays with IC50 values of 65 and 54 μM, respectively. It reduces carrageenan-induced paw edema in rats when administered intravenously at doses ranging from 0.1 to 9 mg/kg. Formulations containing lornoxicam have been used in the management of postoperative pain.

Description

Lornoxicam is a nonselective NSAID for oral and intravenous administration. It has been available for human use since two decades and there is a growing body of evidence supporting its efficacy and tolerability for management of acute pain.
Xefo, a member of the oxicam family of nonsteroidal antiinflammatory agents, was launched in Denmark for mild to moderate pain and inflammation. A seven step synthesis, beginning with 2,5-dichlorothiophene, provides access to this compound. It inhibits prostaglandin synthesis at the level of cyclooxygenase (Cox1 :Cox2 = 0.6) but does not inhibit 5-lipoxygenase. Xefo did not increase serum levels of pepsinogen I (an indicator of gastric mucosal status) and readily penetrates perivascular interstitial spaces including synovial fluid. It is as effective as morphine, meperidine and tramadol in relieving post operative pain and as efficient as other NSAlDs in relieving the symptoms of osteoarthritis and rheumatoid arthritis. It is 100 times more potent than Tenoxicam in inhibiting PGD2 and more active than indomethacin (6x) or piroxicam (10x) in preventing arachadonic acid influenced lethality in mice. Xefo has inhibitor effects on spinal nocicceptive processing presumably via release of endogenous opiods and evidence suggests it is good for migraine.

Chemical Properties

Crystalline Solid

Originator

Nycomed Amersham (Norway)

Uses

For the treatment of acute mild to moderate pain, as well as pain and inflammation of the joints caused by certain types of rheumatic diseases.

Uses

keratolytic, antiacne, antineoplastic

Uses

Cyclooxygenase inhibitor; structurally similar to tenoxicam. Anti-inflammatory; analgesic

Uses

Lornoxicam belongs to the oxicam class. It has anti-inflammatory and antipyretic properties. Lornoxicam prevents the synthesis of prostaglandin (PG) by inhibiting cyclo-oxygenase. It is used to relieve various types of symptoms associated with osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, acute sciatica and low back pain.Lornoxicam is approved for use in Japan.
Lornoxicam has been used as a drug in melanin binding study with cassette dosing and rapid equilibrium dialysis inserts. Lornoxicam differs from other oxicam compounds in its potent inhibition of prostaglandin biosynthesis, a property that explains the particularly pronounced efficacy of the drug.

Indications

Lornoxicam is a non-steroidal anti-inflammatory drug (NSAID) that is used as a painkiller (analgesic). A high level of pain relief is experienced by about 45% of those with moderate to severe postoperative dental pain after a single dose of lornoxicam 8 mg, compared to about 10% with placebo. This is comparable to the proportion experiencing the same level of pain relief with ibuprofen 200 to 400 mg. Adverse events were generally mild and did not differ from placebo in these singe dose studies. There were insufficient data to assess duration of action, but it is likely to be similar to ibuprofen 200 mg.

Definition

ChEBI: A thienothiazine-derived monocarboxylic acid amide obtained by formal condensation of the carboxy group of 6-chloro-4-hydroxy-2-methylthieno[2,3-e][1,2]thiazine-3-carboxylic acid 1,1-dioxide with the amino group of 2-aminopyridine. Used for th treatment of pain, primarily resulting from inflammatory diseases of the joints, osteoarthritis, surgery, sciatica and other inflammations.

brand name

Xefo

in vitro

studies on intact human cells showed that lornoxicam intensively inhibit cox-1 and cox-2 with the lowest ic50 among a large panel of nsaids tested. similar findings were obtained in the whole blood for cox-1/-2. in addition lornoxicam suppressed no formation in a dose-dependently manner with an ic50 of 65 μm. [2]

in vivo

in vivo studies found that lornoxicam was as effective as comparative nsaids and that 8 mg lornoxicam was more effective than 10 mg morphine as a pain-reliever after oral surgery. orally administration of lornoxicam at 16-24 mg daily was more effective than tramadol at 300 mg daily in pain-alleviating after knee surgery. compared to naproxen, lornoxicam showed higher therapeutic potency and lower gastrointestinal toxicity. this was probably due to the short half-life of lornoxicam as compared to the other oxicams. [3]

IC 50

a potent cox-1 and cox-2 inhibitor with ic50 values of 5 nm and 8 nm, respectively.

References

[1]balfour ja, fitton a and barradell lb. lornoxicam, a review of its pharmacology and therapeutic potential in the management of painful and inflammatory conditions. drugs. 1996 apr; 51(4): 639-57.
[2]berg j, fellier h, christoph t, grarup j and stimmeder d. the analgesic nsaid lornoxicam inhibits cyclooxygenase (cox)-1/-2, inducible nitric oxide synthase (inos), and the formation of interleukin (il)-6 in vitro. inflamm res. 1999 jul; 48(7): 369-79.
[3]radhofer-welte s and rabasseda x. lornoxicam, a new potent nsaid with an improved tolerability profile. drugs today (barc). 2000 jan; 36(1): 55-76.
[4]sharma a, pingle a, and baliga vp. lornoxicam efficacy in acute pain (leap) trial. j indian med assoc. 2008 dec; 106(12): 811-3.

504-29-0
70374-39-9
Synthesis of Lornoxicam from 2-Aminopyridine

Lornoxicam Preparation Products And Raw materials

Global( 544)Suppliers
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Hebei Jingbo New Material Technology Co., Ltd
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View Lastest Price from Lornoxicam manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Lornoxicam pictures 2023-12-25 Lornoxicam
70374-39-9
US $8.00 / kg 1kg 99% 200000 Hebei Jingbo New Material Technology Co., Ltd
Lornoxicam;Chlortenoxicam pictures 2023-04-12 Lornoxicam;Chlortenoxicam
70374-39-9
US $1.00 / kg 1kg 99.73%HPLC 5000tons/year Wuhan Dujiang Industrial Co., Ltd.
Lornoxicam pictures 2023-03-27 Lornoxicam
70374-39-9
US $12.00 / KG 1KG 0.99 25t XINGTAI XINGJIU NEW MATERIAL TECHNOLOGY CO., LTD
  • Lornoxicam pictures
  • Lornoxicam
    70374-39-9
  • US $8.00 / kg
  • 99%
  • Hebei Jingbo New Material Technology Co., Ltd
  • Lornoxicam pictures
  • Lornoxicam
    70374-39-9
  • US $12.00 / KG
  • 0.99
  • XINGTAI XINGJIU NEW MATERIAL TECHNOLOGY CO., LTD

Lornoxicam Spectrum

LORNOXICAM AKOS 93662 6-Chloro-4-hydroxy-2-methyl-N-(2-pyridyl)-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide 1,1-dioxide LornoxicaM for injection 6-Chloro-4-hydroxy-2-Methyl-N-2-pyridinyl- LornoxicaM API 6-Chloro-4-hydroxy-2-Methyl-N-pyridin-2-yl-2H-thieno[2,3-e][1,2]thiazine-3-carboxaMide LornoxicaM (Xefo) 6-Chloro-4-hydroxy-2-methyl-N-pyridin-2-yl-2H-thie no[2,3-e][1,2]thiazine-3-carboxamide 1,1-dioxi 1,1-dioxide-6-chloro-4-hydroxy-2-methyl-N-2-pyridinyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 6-Chloro-4-hydroxy-2-methyl-N-pyridin-2-yl-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide 1,1-dio 6-CHLORO-4-HYDROXY-2-METHYL-N-2-PYRIDINYL-2H-THIENO[2,3-E]-1,2-THIAZINE-3-CARBOXAMIDE 1,1-DIOXIDE 2h-thieno(2,3-e)-1,2-thiazine-3-carboxamide,6-chloro-4-hydroxy-2-methyl-n-2-py chlortenoxicam ridinyl-,1,1-dioxide 6-Chloro-4-hydroxy-2-methyl-N-pyridin-2-yl-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide-1,1-dioxide LornoxicamConsultedStandard Ro 13-9297 Telos TS 110 Xefo Xefocam 6-Chloro-4-hydroxy-2-methyl-N-2-pyridinyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamidel,1-dioxide Lornoxicam, 98%, a non-steroidal COX-1/COX-2 inhibitor (3Z)-6-chloro-3-[hydroxy-(2-pyridinylamino)methylidene]-2-methyl-1,1-dioxo-4-thieno[2,3-e]thiazinone Lornoxicam> ornoxicam 6-chloro-4-hydroxy-2-methyl-1,1-dioxo-N-(pyridin-2-yl)-2H-1$l^{6},5,2-thieno[2,3-e][1$l^{6},2]thiazine-3-carboxamide 2H-Thieno[2,3-e]-1,2-thiazine-3-carboxamide, 6-chloro-4-hydroxy-2-methyl-N-2-pyridinyl-, 1,1-dioxide Lornoxicam USP/EP/BP Lornoxicam (Chlortenoxicam LornoxicamQ: What is Lornoxicam Q: What is the CAS Number of Lornoxicam Q: What is the storage condition of Lornoxicam Q: What are the applications of Lornoxicam 6-Chloro-4-hydroxy-2-methyl-N-pyridin-2-yl-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide 1,1-dioxide (Lornoxicam) Lornoxicam Impurity 33 Yesterday, the chlorine methyl 5-chloro-3-(ethoxysulfonyl)thiophene-2-carboxylate Lornoxicam INH Lornoxicam, ≥ 98.0% 70374-39-9 原料药 > 解热镇痛药 > 非甾抗炎药 > 氯诺昔康 C13H10ClN3O4S2 Sulfur & Selenium Compounds Pharmaceuticals Intermediates & Fine Chemicals Inhibitors APIs Fused Ring Systems API Other APIs AVITA 70374-39-9