P5640
Prostaglandin E2
≥93% (HPLC), synthetic
Manufacturer: Sigma Aldrich
CAS Number: 363-24-6
Synonym(S): (5Z,11α,13E,15S)-11,15-Dihydroxy-9-oxoprosta-5,13-dienoic acid, Dinoprostone, PGE2
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 MG | P5640-1-MG | In Stock | ₹ 16,529.78 |
| 5 MG | P5640-5-MG | In Stock | ₹ 32,420.88 |
| 10 MG | P5640-10-MG | In Stock | ₹ 58,898.83 |
P5640 - 1 MG
In Stock
Quantity
1
Base Price: ₹ 16,529.78
GST (18%): ₹ 2,975.36
Total Price: ₹ 19,505.14
biological source
synthetic
Quality Level
200
Assay
≥93% (HPLC)
form
powder
functional group
carboxylic acidhydroxyl
shipped in
ambient
storage temp.
−20°C
SMILES string
O[C@@H]1CC([C@H](C/C=C\CCCC(O)=O)[C@H]1/C=C/[C@@H](O)CCCCC)=O
InChI
1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,15-17,19,21,23H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16+,17+,19+/m0/s1
InChI key
XEYBRNLFEZDVAW-ARSRFYASSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Enzo Life Sciences Prostaglandin E2, (1mg), CAS Number: 363-24-6 | Enzo Life Sciences | ₹ 3,935.76 | |
 | Selleck Chemical LLC Prostaglandin E2 (PGE2) 5mg 363-24-6 Dinoprostone | Selleck Chemical LLC | ₹ 15,092.78 | |
 | Cayman Chemical Prostaglandin E2, 363-24-6, 10 mg | Cayman Chemical | ₹ 13,283.19 | |
 | Sigma Aldrich Fine Chemicals Biosciences Prostaglandin E2, 363-24-6, MFCD00077861, 1mg | Sigma Aldrich Fine Chemicals Biosciences | ₹ 35,950.60 | |
 | Sigma Aldrich Fine Chemicals Biosciences Prostaglandin E2 synthetic, powder, BioReagent, suitable for cell culture, 363-24-6, MFCD00077861 | Sigma Aldrich Fine Chemicals Biosciences | ₹ 28,298.97 | |
 | Prostaglandin E2 | Sigma Aldrich | ₹ 27,647.05 - ₹ 1,25,310.20 | |
| | Prostaglandin E2 | Sigma Aldrich | ₹ 36,924.08 | |
| | Prostaglandin E2 | Sigma Aldrich | ₹ 36,924.08 | |
 | 363-24-6 | (5Z,11α,13E,15S)-11,15-dihydroxy-9-oxoprosta-5,13-dien-1-oic acid | A2B Chem | ₹ 2,053.44 - ₹ 65,196.72 |
Related Products
Description
- Application: Post-resolution macrophages shape long-term tissue immunity and integrity in a mouse model of pneumococcal pneumonia.: Investigating the influence of prostaglandin E2 within the resolution phase of inflammation, this study demonstrates its essential role in macrophage-mediated tissue repair and immune memory following bacterial lung infections, providing insights into immune system regulation and recovery processes (Feehan et al., 2024).
- Biochem/physiol Actions: Most biologically active prostaglandin. PGE2 induces cervical ripening and parturition; mediates bradykinin-induced vasodilation; regulates adenylyl cyclase. Tumor cells that over-express cyclooxygenase 2 display increased invasiveness, angiogenesis, and resistance to apoptosis that may be due to the PGE2-induced expression of angiogenic factors and stabilization of the anti-apoptotic protein, survivin.The effect of PGE2 on the immune system is mixed. It inhibits T cell activation in vitro, suggesting it is an immunosuppressant. However, in vivo, it appears to effect expansion of the Th17 subset and differentiation of the Th1 subset of T helper cells, marking it as an immunoactivator.
SAFETY INFORMATION
Pictograms
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Repr. 1B
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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biological source: synthetic
Quality Level: 200
Assay: ≥93% (HPLC)
form: powder
functional group: carboxylic acidhydroxyl
shipped in: ambient
storage temp.: −20°C
SMILES string: O[C@@H]1CC([C@H](C/C=C\CCCC(O)=O)[C@H]1/C=C/[C@@H](O)CCCCC)=O
InChI: 1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,15-17,19,21,23H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16+,17+,19+/m0/s1
InChI key: XEYBRNLFEZDVAW-ARSRFYASSA-N
biological source:
synthetic
Quality Level:
200
Assay:
≥93% (HPLC)
form:
powder
functional group:
carboxylic acidhydroxyl
shipped in:
ambient
storage temp.:
−20°C
SMILES string:
O[C@@H]1CC([C@H](C/C=C\CCCC(O)=O)[C@H]1/C=C/[C@@H](O)CCCCC)=O
InChI:
1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,15-17,19,21,23H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16+,17+,19+/m0/s1
InChI key:
XEYBRNLFEZDVAW-ARSRFYASSA-N
biological source: __
Quality Level: 200
Assay: ≥99.0%
form: powder
functional group: __
shipped in: __
storage temp.: __
SMILES string: __
InChI: __
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biological source:
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Quality Level:
200
Assay:
≥99.0%
form:
powder
functional group:
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shipped in:
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storage temp.:
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SMILES string:
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InChI:
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InChI key:
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biological source: __
Quality Level: 200
Assay: ≥99.0%
form: powder
functional group: __
shipped in: __
storage temp.: __
SMILES string: __
InChI: __
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biological source:
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Quality Level:
200
Assay:
≥99.0%
form:
powder
functional group:
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shipped in:
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storage temp.:
__
SMILES string:
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InChI:
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InChI key:
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biological source: __
Quality Level: 200
Assay: ≥99.0%
form: powder
functional group: __
shipped in: __
storage temp.: __
SMILES string: __
InChI: __
InChI key: __
biological source:
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Quality Level:
200
Assay:
≥99.0%
form:
powder
functional group:
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shipped in:
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storage temp.:
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SMILES string:
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InChI:
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InChI key:
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