LEUKOTRIENE D4
- Product Name
- LEUKOTRIENE D4
- CAS No.
- 73836-78-9
- Chemical Name
- LEUKOTRIENE D4
- Synonyms
- LTD4;leukotriened;LEUKOTRIENE D4;leukotriened(sub4);LTD4 (Leukotriene D4);Leukotriene D4 (LTD4);Leukotriene D4;YEESKJGWJFYOOK-IJHYULJSSA-N;(r-(r*,s*-(e,e,z,z)))-inyl);Leukotriene D4 MaxSpecStandard
- CBNumber
- CB1283439
- Molecular Formula
- C25H40N2O6S
- Formula Weight
- 496.66
- MOL File
- 73836-78-9.mol
LEUKOTRIENE D4 Property
- Boiling point:
- 785.8±60.0 °C(Predicted)
- Density
- 1.162±0.06 g/cm3(Predicted)
- Flash point:
- 9℃
- storage temp.
- -70°C
- solubility
- A solution in ethanol
- form
- Liquid.
- pka
- 3.03±0.10(Predicted)
- color
- Colorless to light yellow
Safety
- Hazard Codes
- F,T
- Risk Statements
- 11-23/24/25-39/23/24/25
- Safety Statements
- 7-16-36/37-45
- RIDADR
- UN 1230 3/PG 2
- WGK Germany
- 3
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H225Highly Flammable liquid and vapour
H370Causes damage to organs
- Precautionary statements
-
P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P280Wear protective gloves/protective clothing/eye protection/face protection.
N-Bromosuccinimide Price
- Product number
- L5011
- Product name
- Leukotriene D4
- Purity
- ~50?μg/mL (in methanol/ammonium acetate buffer, 70:30, pH 5.6), ≥97%
- Packaging
- 10μg
- Price
- $326
- Updated
- 2025/07/31
- Product number
- L5011
- Product name
- Leukotriene D4
- Purity
- ~50?μg/mL (in methanol/ammonium acetate buffer, 70:30, pH 5.6), ≥97%
- Packaging
- 25μg
- Price
- $647
- Updated
- 2025/07/31
- Product number
- L5011
- Product name
- Leukotriene D4
- Purity
- ~50?μg/mL (in methanol/ammonium acetate buffer, 70:30, pH 5.6), ≥97%
- Packaging
- 50μg
- Price
- $977
- Updated
- 2025/07/31
- Product number
- L5011
- Product name
- Leukotriene D4
- Purity
- ~50?μg/mL (in methanol/ammonium acetate buffer, 70:30, pH 5.6), ≥97%
- Packaging
- 250μg
- Price
- $2130
- Updated
- 2022/05/15
- Product number
- 20310
- Product name
- Leukotriene D4
- Purity
- ≥97%
- Packaging
- 25μg
- Price
- $144
- Updated
- 2024/03/01
LEUKOTRIENE D4 Chemical Properties,Usage,Production
Description
Leukotriene D4 (LTD4) is an active metabolite of LTC4 (Item Nos. 20210 | 10007241) and a constituent of slow-reacting substance of anaphylaxis (SRS-A). It is formed via metabolism of LTC4 by γ-glutamyl transpeptidase. Like LTC4, LTD4 (0.01-0.1 pM) induces contractions in isolated guinea pig parenchymal strips and tracheal spirals. In vivo, LTD4 increases insufflation pressure, a marker of bronchoconstriction, in anesthetized guinea pigs by 100% when administered at a dose of 89 pmol per animal. It also increases vascular permeability in guinea pig skin when administered intradermally at a dose of 0.1 pmol per animal.
Uses
LTD4 (Leukotriene D4) is a member of the leukotriene family shown to be a potent contractor of smooth muscle.
Definition
ChEBI: A leukotriene that is (7E,9E,11Z,14Z)-icosa-7,9,11,14-tetraenoic acid substituted by a hydroxy group at position 5 (5S) and a L-cysteinylglycinyl group at position 6 (6R).
Biochem/physiol Actions
Slow reacting substance of anaphylaxis (SRS-A). Potent bronchoconstrictor and mediator of asthmatic and inflammatory processes. Increases cytosolic free Ca2+ in epithelial cells.
in vivo
Leukotriene D4 (1.5, 3, 6, 12, 24 μg/paw; injected intradermally) causes edema and increases capillary permeability in a dose-related manner in mouse[2].
| Animal Model: | 21-24 g, Balb/c male mice[2] |
| Dosage: | 1.5, 3, 6, 12, 24 μg/paw |
| Administration: | Injected intradermally (10 μL was injected into the left hind paw) |
| Result: | Caused significant edematous response and dye extravasation at doses of 1.5-6 ~g/paw. |
IC 50
Human Endogenous Metabolite
References
[1] L ORNING B S S Hammarstr?m. Leukotriene D: a slow reacting substance from rat basophilic leukemia cells.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1980, 77 4: 2014-2017. DOI: 10.1073/pnas.77.4.2014
[2] S HAMMARSTR?M K B L Orning. Metabolism of leukotrienes.[J]. Molecular and Cellular Biochemistry, 1985, 69 1: 7-16. DOI: 10.1007/bf00225922
[3] PER HEDQVIST. Biological profile of Ieukotrienes C4 and D4[J]. Acta Physiologica, 1980, 110 3: 331-333. DOI: 10.1111/j.1748-1716.1980.tb06676.x
[4] EMILIE CERAUDO. Direct evidence that the GPCR CysLTR2 mutant causative of uveal melanoma is constitutively active with highly biased signaling.[J]. The Journal of Biological Chemistry, 2021: 100163. DOI: 10.1074/jbc.ra120.015352
[5] ERICK LU. S-Geranylgeranyl-l-glutathione is a ligand for human B cell-confinement receptor P2RY8[J]. Nature, 2019, 567 7747: 244-248. DOI: 10.1038/s41586-019-1003-z
[6] NATHAN C NI. A selective cysteinyl leukotriene receptor 2 antagonist blocks myocardial ischemia/reperfusion injury and vascular permeability in mice.[J]. Journal of Pharmacology and Experimental Therapeutics, 2011, 339 3: 768-778. DOI: 10.1124/jpet.111.186031
[7] HAI-YAN QI. A cytosolic phospholipase A2-initiated lipid mediator pathway induces autophagy in macrophages.[J]. Journal of immunology, 2011, 187 10: 5286-5292. DOI: 10.4049/jimmunol.1004004
[8] E. ONO. Concentration of 14,15-leukotriene C4 (eoxin C4) in bronchoalveolar lavage fluid[J]. Clinical and Experimental Allergy, 2009, 39 9: 1348-1352. DOI: 10.1111/j.1365-2222.2009.03261.x
[9] PEDRO P MEDINA Montse S C Montse Sanchez Cespedes. Involvement of the chromatin-remodeling factor BRG1/SMARCA4 in human cancer.[J]. Epigenetics, 2008, 3 2: 64-68. DOI: 10.4161/epi.3.2.6153
[10] KARSTEN GRONERT. Selectivity of Recombinant Human Leukotriene D4, Leukotriene B4, and Lipoxin A4 Receptors with Aspirin-Triggered 15-epi-LXA4 and Regulation of Vascular and Inflammatory Responses[J]. American Journal of Pathology, 2001, 158 1: Pages 3-9. DOI: 10.1016/s0002-9440(10)63937-5
LEUKOTRIENE D4 Preparation Products And Raw materials
Raw materials
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