A crystalline solid form of latanoprost (free acid)
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Latanoprost (free acid) (L-arginine salt)

Item No. 10008432

Technical Information
Formal Name
(Z)-7-((1R,2R,3R,5S)-3,5-dihydroxy-2-((R)-3-hydroxy-5-phenylpentyl)cyclopentyl)hept-5-enoic acid, L-arginine salt
Synonyms
  • PhXA-85
  • 17-phenyl-13,14-dihydro trinor Prostaglandin F
Molecular Formula
C29H48N4O7
Formula Weight
Purity
≥95%
Formulation
A solid
Acetonitrile: Slightly soluble: 0.1-1 mg/mlMethanol: Slightly soluble: 0.1-1 mg/ml
SMILES
O[C@@H]1[C@H](C/C=C\CCCC(O)=O)[C@@H](CC[C@@H](O)CCC2=CC=CC=C2)[C@H](O)C1.[NH3+]C(NCCC[C@@H](N)C([O-])=O)=N
InChi Code
InChI=1S/C23H34O5.C6H14N4O2/c24-18(13-12-17-8-4-3-5-9-17)14-15-20-19(21(25)16-22(20)26)10-6-1-2-7-11-23(27)28;7-4(5(11)12)2-1-3-10-6(8)9/h1,3-6,8-9,18-22,24-26H,2,7,10-16H2,(H,27,28);4H,1-3,7H2,(H,11,12)(H4,8,9,10)/b6-1-;/t18-,19+,20+,21-,22+;/m0./s1
InChi Key
KSGLGRAPOOXCBD-HGAMFJTGSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    Latanoprost (free acid) (L-arginine salt) is a salt form of latanoprost (free acid) (Item No. 16811) that results in a crystalline solid.1 This solid form of latanoprost improves ease of handling, making it ideal for use as a synthetic intermediate and for compounding it into mixtures with other components. Latanoprost (free acid) is a derivative of prostaglandin F (PGF; Item Nos. 16010 | 16020), an FP receptor agonist, and an active metabolite of the prodrug latanoprost (Item No. 16812).2 It selectively binds to the FP receptor (Ki = 0.098 µM) over the EP1, EP1, EP3, and EP4 receptors (Kis = 2.06, 39.667, 7.519, and 75 µM, respectively), as well as the DP, IP, and TP receptors (Kis = ≥20, ≥90, and ≥60 µM, respectively). It induces phosphoinositide turnover in isolated human ciliary muscle and human trabecular meshwork cells, mouse NIH3T3 fibroblasts, and rat A7r5 vascular smooth muscle cells, which all endogenously express FP receptors (EC50s = 124, 35, 32, and 35 nM, respectively), as well as HEK293 cells expressing human ocular FP receptors (EC50 = 45.7 nM). It also increases intracellular calcium levels in hEP1-5/293-AEQ17 cells expressing EP1 receptors in an aequorin-based calcium assay (EC50 = 119 nM).3 Latanoprost (free acid) induces contraction of isolated cat iris sphincter smooth muscle (EC50 = 29.9 nM).4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. DeLong, M.A., and Sturdivant, J.M. Amino acid salts of prostaglandins. (2009).

    2. Sharif, N.A., Kelly, C.R., Crider, J.Y., et alOcular hypotensive FP prostaglandin (PG) analogs: PG receptor subtype binding affinities and selectivities, and agonist potencies at FP and other PG receptors in cultured cells. J. Ocul. Pharmacol. Ther. 19(6), 501-515 (2003).

    3. Ungrin, M.D., Carrière, M.C., Denis, D., et alKey structural features of prostaglandin E2 and prostanoid analogs involved in binding and activation of the human EP1 prostanoid receptor. Mol. Pharmacol. 59(6), 1446-1456 (2001).

    4. Sharif, N.A., Kaddour-Djebbar, I., and Abdel-Latif, A.A. Cat iris sphincter smooth-muscle contraction: Comparison of FP-class prostaglandin analog agonist activities. J. Ocul. Pharmacol. Ther. 24(2), 152-163 (2008).