N 0164

    WARNING: This product is for research use only, not for human or veterinary use.

Hodoodo CAT#: H534875

CAS#: 60787-00-0

Description: N 0164 is a bioactive chemical.


Chemical Structure

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N 0164
CAS# 60787-00-0

Theoretical Analysis

Hodoodo Cat#: H534875
Name: N 0164
CAS#: 60787-00-0
Chemical Formula: C29H25ClNaO4P
Exact Mass: 526.11
Molecular Weight: 526.929
Elemental Analysis: C, 66.10; H, 4.78; Cl, 6.73; Na, 4.36; O, 12.15; P, 5.88

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @hodoodo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: N 0164; N-0164; N0164

IUPAC/Chemical Name: (Phenylmethyl)phosphonic acid, mono(4-(2-((4-chlorophenyl)methyl)-1-oxo-3-phenylpropyl)phenyl) ester, sodium salt

InChi Key: RIYADZCUQWEJEP-UHFFFAOYSA-M

InChi Code: InChI=1S/C29H26ClO4P.Na/c30-27-15-11-23(12-16-27)20-26(19-22-7-3-1-4-8-22)29(31)25-13-17-28(18-14-25)34-35(32,33)21-24-9-5-2-6-10-24;/h1-18,26H,19-21H2,(H,32,33);/q;+1/p-1

SMILES Code: [O-]P(CC1=CC=CC=C1)(OC2=CC=C(C(C(CC3=CC=C(Cl)C=C3)CC4=CC=CC=C4)=O)C=C2)=O.[Na+]

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >3 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 526.93 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Allan G, Levi R. The cardiac effects of prostaglandins and their modification by the prostaglandin antagonist N-0164. J Pharmacol Exp Ther. 1980 Jul;214(1):45-9. PMID: 6993659.


2: Eakins KE, Rajadhyaksha V, Schroer R. Prostaglandin antagonism by sodium p-benzyl-4-[1-oxo-2-(4-chlorobenzyl)-3-phenylpropyl]pheenyl phosphonate (N-0164). Br J Pharmacol. 1976 Nov;58(3):333-9. doi: 10.1111/j.1476-5381.1976.tb07709.x. PMID: 990588; PMCID: PMC1667574.


3: Maas AJ, Den Hertog A. The effect of the phenyl phosphonate N-0164 on prostaglandin action and on post inhibitory excitation in the taenia of guinea- pig caecum. Eur J Pharmacol. 1980 Mar 21;62(2-3):157-66. doi: 10.1016/0014-2999(80)90272-1. PMID: 7379838.


4: Tynan SS, Andersen NH, Wills MT, Harker LA, Hanson SR. On the multiplicity of platelet prostaglandin receptors. II. The use of N-0164 for distinguishing the loci of action for PGI2, PGD2, PGE2 and hydantoin analogs. Prostaglandins. 1984 May;27(5):683-96. doi: 10.1016/0090-6980(84)90007-8. PMID: 6087417.


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6: Vulliemoz Y, Verosky M, Triner L. Effect of a prostaglandin antagonist, N-0164, on cAMP generation and hydrolysis in the rat uterus. Biochem Pharmacol. 1981 Jul 15;30(14):1941-6. doi: 10.1016/0006-2952(81)90203-3. PMID: 6268114.


7: Botting JH, Linton EA, Whitehead SA. Blockade of ovulation in the rat by a prostaglandin antogonist (N-0164). J Endocrinol. 1977 Nov;75(2):335-6. doi: 10.1677/joe.0.0750335. PMID: 591817.


8: Kulkarni PS, Eakins KE. N-0164 inhibits generation of thromboxane-A2-like activity from prostaglandin endoperoxides by human platelet microsomes. Prostaglandins. 1976 Sep;12(3):465-9. doi: 10.1016/0090-6980(76)90027-7. PMID: 968059.


9: Eakins KE, Kulkarni PS. Selective inhibitory actions of sodium-p- benzyl-4-[1-oxo-2-(4-chlorobenzyl)-3-phenyl propyl] phenyl phosphonate (N-0161) and indomethacin on the biosynthesis of prostaglandins and thromboxanes from arachidonic acid. Br J Pharmacol. 1977 May;60(1):135-40. doi: 10.1111/j.1476-5381.1977.tb16757.x. PMID: 884384; PMCID: PMC1667177.


10: Chatain GP, Patronas N, Smirniotopoulos JG, Piazza M, Benzo S, Ray-Chaudhury A, Sharma S, Lodish M, Nieman L, Stratakis CA, Chittiboina P. Potential utility of FLAIR in MRI-negative Cushing's disease. J Neurosurg. 2018 Sep;129(3):620-628. doi: 10.3171/2017.4.JNS17234. Epub 2017 Oct 13. PMID: 29027863; PMCID: PMC6398169.


11: Hamid-Bloomfield S, Whittle BJ. Prostaglandin D2 interacts at thromboxane receptor-sites on guinea-pig platelets. Br J Pharmacol. 1986 Aug;88(4):931-6. doi: 10.1111/j.1476-5381.1986.tb16268.x. PMID: 3017497; PMCID: PMC1917072.


12: Brus R, Zabawska J. Anagoniści prostaglandyn [Prostaglandin antagonists]. Postepy Hig Med Dosw. 1980 Nov-Dec;33(6):677-91. Polish. PMID: 6104329.


13: Schlicker E, Fink K, Göthert M. Influence of eicosanoids on serotonin release in the rat brain: inhibition by prostaglandins E1 and E2. Naunyn Schmiedebergs Arch Pharmacol. 1987 Jun;335(6):646-51. doi: 10.1007/BF00166981. PMID: 3476858.


14: Manku MS, Horrobin DF, Oka M, Ally AI, Karmazyn M, Cunnane SC, Morgan RO, Karmali RA. Ultra-violet radiation and 8-methoxypsoralen have actions similar to those of known inhibitors of thromboxane A2 synthesis in rat mesenteric blood vessels. Prostaglandins Med. 1978 Jul;1(1):86-95. doi: 10.1016/0161-4630(78)90080-0. PMID: 715050.


15: Hattori Y, Levi R. Effect of PGD2 on cardiac contractility: a negative inotropism secondary to coronary vasoconstriction conceals a primary positive inotropic action. J Pharmacol Exp Ther. 1986 Jun;237(3):719-24. PMID: 3012066.


16: Whittle BJ, Moncada S, Vane JR. Comparison of the effects of prostacyclin (PGI2), prostaglandin E1 and D2 on platelet aggregation in different species. Prostaglandins. 1978 Sep;16(3):373-88. doi: 10.1016/0090-6980(78)90216-2. PMID: 364545.


17: Kangasaho M, Vapaatalo H. TXA2-antagonistic properties of agents affecting prostaglandin synthesis or the cyclic nucleotide system in human platelets. Acta Pharmacol Toxicol (Copenh). 1983 Aug;53(2):130-4. doi: 10.1111/j.1600-0773.1983.tb01880.x. PMID: 6624480.


18: Seiler S, Brassard CL, Federici ME. SQ-27986 inhibition of platelet aggregation is mediated through activation of platelet prostaglandin D2 receptors. Prostaglandins. 1990 Aug;40(2):119-30. doi: 10.1016/0090-6980(90)90078-a. PMID: 2171039.


19: Kelly JP, Johnson MC, Parker CW. Effect of inhibitors of arachidonic acid metabolism on mitogenesis in human lymphocytes: possible role of thromboxanes and products of the lipoxygenase pathway. J Immunol. 1979 Apr;122(4):1563-71. PMID: 109510.


20: Miller OV, Gorman RR. Evidence for distinct prostaglandin I2 and D2 receptors in human platelets. J Pharmacol Exp Ther. 1979 Jul;210(1):134-40. PMID: 221643.