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INDOMETHACIN ESTER, N-HEPTYL-

Product Name
INDOMETHACIN ESTER, N-HEPTYL-
CAS No.
282728-47-6
Chemical Name
INDOMETHACIN ESTER, N-HEPTYL-
Synonyms
INDOMETHACIN HEPTYL ESTER;PYBCHCVNKGZCOH-UHFFFAOYSA-N;INDOMETHACIN ESTER, N-HEPTYL-;Indomethacin heptyl ester, 10 mM in DMSO;1H-Indole-3-acetic acid, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-, heptyl ester;1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOLE-3-ACETIC ACID, 1-HEPTYL ESTER;1-(P-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOLE-3-ACETIC ACID, N-HEPTYL ESTER;1-(P-CHLOROBENZOYL)-5-METHOXY-3-METHYL-1H-INDOLE-3-ACETIC ACID, N-HEPTYL ESTER
CBNumber
CB5105498
Molecular Formula
C26H30ClNO4
Formula Weight
455.97
MOL File
Mol file
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INDOMETHACIN ESTER, N-HEPTYL- Property

Flash point:
-16 °C
storage temp. 
−20°C
solubility 
≤17mg/ml in ethanol;17mg/ml in DMSO;17mg/ml in dimethyl formamide
form 
methyl acetate solution
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Safety

Hazard Codes 
F,Xi
Risk Statements 
11-36-66-67
Safety Statements 
16-26-29-33-36
RIDADR 
UN 1231 3/PG 2
WGK Germany 
1
RTECS 
AI9100000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H319Causes serious eye irritation

H336May cause drowsiness or dizziness

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

P242Use only non-sparking tools.

P243Take precautionary measures against static discharge.

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P312Call a POISON CENTER or doctor/physician if you feel unwell.

P337+P313IF eye irritation persists: Get medical advice/attention.

P370+P378In case of fire: Use … for extinction.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

P403+P235Store in a well-ventilated place. Keep cool.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Cayman Chemical
Product number
70271
Product name
Indomethacin heptyl ester
Purity
≥98%
Packaging
1mg
Price
$25
Updated
2024/03/01
Cayman Chemical
Product number
70271
Product name
Indomethacin heptyl ester
Purity
≥98%
Packaging
5mg
Price
$107
Updated
2024/03/01
Cayman Chemical
Product number
70271
Product name
Indomethacin heptyl ester
Purity
≥98%
Packaging
10mg
Price
$186
Updated
2024/03/01
Cayman Chemical
Product number
70271
Product name
Indomethacin heptyl ester
Purity
≥98%
Packaging
50mg
Price
$807
Updated
2024/03/01
AK Scientific
Product number
7192CR
Product name
Indomethacinheptylester
Packaging
1mg
Price
$125
Updated
2021/12/16
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INDOMETHACIN ESTER, N-HEPTYL- Chemical Properties,Usage,Production

Description

Indomethacin is a potent but non-selective inhibitor of both COX-1 and COX-2 in sheep and humans. Structurally, indomethacin is a substituted indole acetic acid, wherein the carboxylate can be derivatized as an ester or amide. These derivatives show enhanced selectivity for the COX-2 isoform. For example, the IC50 for indomethacin heptyl ester for the inhibition of human recombinant COX-2 is 0.04 μM, making it more than 1,700 times more potent as an inhibitor of COX-2 than COX-1. While indomethacin itself has an IC50 of 0.05 μM for the inhibition of COX-2, it also inhibits COX-1 with a corresponding IC50 of 0.67 μM.

Uses

Indomethacin heptyl ester is a selective COX-2 inhibitor with IC50 of 0.04 μM, exhibits anti-inflammatory activity[1].

Definition

ChEBI: Indomethacin heptyl ester is a N-acylindole.

References

[1]. kalgutkar as, marnett ab, crews bc, et al. ester and amide derivatives of the nonsteroidal antiinflammatory drug, indomethacin, as selective cyclooxygenase-2 inhibitors. j med chem. 2000 jul 27;43(15):2860-70.

INDOMETHACIN ESTER, N-HEPTYL- Preparation Products And Raw materials

Raw materials

Preparation Products

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INDOMETHACIN ESTER, N-HEPTYL- Suppliers

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282728-47-6, INDOMETHACIN ESTER, N-HEPTYL-Related Search:


  • PYBCHCVNKGZCOH-UHFFFAOYSA-N
  • INDOMETHACIN ESTER, N-HEPTYL-
  • INDOMETHACIN HEPTYL ESTER
  • 1-(P-CHLOROBENZOYL)-5-METHOXY-3-METHYL-1H-INDOLE-3-ACETIC ACID, N-HEPTYL ESTER
  • 1-(P-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOLE-3-ACETIC ACID, N-HEPTYL ESTER
  • 1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOLE-3-ACETIC ACID, 1-HEPTYL ESTER
  • 1H-Indole-3-acetic acid, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-, heptyl ester
  • Indomethacin heptyl ester, 10 mM in DMSO
  • 282728-47-6
  • Enzymes, Inhibitors, and Substrates
  • Cyclooxygenase (COX) Enzymes
  • Cyclooxygenase Inhibitors
  • Cell Signaling Enzymes
  • Application Index
  • Biochemicals and Reagents
  • BioChemical
  • Cyclooxygenase InhibitorsCancer Research
  • A to
  • Arachidonic Acid Cascade
  • Chemopreventive Agents
  • Cyclooxygenase (COX) Enzymes
  • CyclooxygenaseCell Signaling Enzymes
  • CyclooxygenaseEnzyme Inhibitors by Enzyme
  • Enzyme Inhibitors