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Ciproxifan

CAS No.
184025-18-1
Chemical Name:
Ciproxifan
Synonyms
CS-757;FUB 359;Ciproxifan, >=99%;Ciproxifan (FUB-359);Ciproxifan USP/EP/BP;Cyclopropyl[4-[3-(1H-imidazol-5-yl)propoxy]phenyl]methanone;Methanone, cyclopropyl[4-[3-(1H-imidazol-5-yl)propoxy]phenyl]-;Methanone, cyclopropyl[4-[3-(1H-iMidazol-4-yl)propoxy]phenyl]-
CBNumber:
CB2503297
Molecular Formula:
C16H18N2O2
Molecular Weight:
270.33
MDL Number:
MFCD00951610
MOL File:
184025-18-1.mol
Last updated:2023-05-18 11:31:10

Ciproxifan Properties

Boiling point 526.9±35.0 °C(Predicted)
Density 1.231
storage temp. 2-8°C
solubility H2O: insoluble
pka 14.54±0.10(Predicted)
form solid
color white
FDA UNII 5EVQ7IRG99

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xn
Risk Statements  22-36/37/38-43
Safety Statements  26-36/37/39
WGK Germany  3

Ciproxifan price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation INB0000417 CIPROXIFAN 95.00% 184025-18-1 5MG $501.17 2021-12-16 Buy
Biorbyt Ltd orb180766 Ciproxifan (FUB-359) >98% 184025-18-1 100mg $615.4 2021-12-16 Buy
ApexBio Technology B1570 Ciproxifan 184025-18-1 50mg $756 2021-12-16 Buy
Biorbyt Ltd orb180766 Ciproxifan (FUB-359) >98% 184025-18-1 250mg $1208.7 2021-12-16 Buy
Biorbyt Ltd orb180766 Ciproxifan (FUB-359) >98% 184025-18-1 1g $2395.3 2021-12-16 Buy
Product number Packaging Price Buy
INB0000417 5MG $501.17 Buy
orb180766 100mg $615.4 Buy
B1570 50mg $756 Buy
orb180766 250mg $1208.7 Buy
orb180766 1g $2395.3 Buy

Ciproxifan Chemical Properties,Uses,Production

Definition

ChEBI: Cyclopropyl-[4-[3-(1H-imidazol-5-yl)propoxy]phenyl]methanone is an aromatic ketone.

Biological Activity

ciproxifan is a novel and potent antagonist of histamine h3-receptor with a ic50 value of 9.2±1.8nm [1].ciproxifan has shown the in-vitro antagonistic action to h3-receptor with a ic50 value of 9.2±1.8nm. in addition, ciproxifan has been reported to competitively antagonize the (r) α-meha induced relaxation of electrically stimulated guinea pig ileum longitudinal muscle. besides, ciproxifan has been revealed to have the effect on [125i]iodoproxyfan binding with a ki value of 0.7±0.2 nm. apart from these, ciproxifan has been found to be a selective antagonist with pki values of 9.3, 4.9, 4.6, 5.5, 5.4, 4.9, <5.0, 4.8, <5.5 and <5.7 for h3, h2, h1, muscarinic m3, adrenergic α1d, β1, serotonin 5-ht1b, 5-ht2a, 5-ht3 and 5-ht4, respectively [1].

in vitro

Ciproxifan inhibits [3H]HA release from synaptosomes with Ki of 0.5 nM. It inhibits the binding of [125I]iodoproxyfan at the brain H3 receptor with Ki of 0.7 nM. It displays high affinity at H3 receptor but shows low apparent affinity at other receptor subtypes as evaluated in functional tests on isolated organs ( histamine H1 and H2, muscarinic M3, adrenergic α1D and β1, serotonin 5-HT1B, 5-HT2A, 5-HT3 and 5-HT4 >).

in vivo

Ciproxifan intravenously injected at dose of 1 mg/kg decreases the H3-receptor ligand concentration in serum in Male Swiss mice, with half-times of distribution phase of 13 min and elimination phase of 87 min, respectively. Ciproxifan (1 mg/kg, po) rises brain t-MeHA level rapidly in Male Swiss mice, being already significantly increased after 30 min, reaching a plateau between 90 and 180 min and still remaining enhanced after 270 min. It leads to ED50 values of 0.23 mg/kg in cerebral cortex, 0.28 mg/kg in striatum and 0.30 mg/kg in hypothalamus in Male Wistar rats. It (3 mg/kg, ip) significantly increased choice accuracy as evaluated in the five-choice task performed using a short stimulus duration. Ciproxifan (0.15-2 mg/kg, po) induces marked signs of neocortical electroencephalogram activation manifested by enhanced fast-rhythms density and an almost total waking state in cats. Ciproxifan (10 mg/kg ip) enhances prepulse inhibition in the DBA/2 strain mice. It (3 mg/kg ip) alleviates hyperactivity and cognitive deficits in the APP Tg2576 mouse model of Alzheimer's disease. Ciproxifan (3 mg/kg ip) improves accuracy and decreased impulsivity in adult male hooded Lister rats.

References

[1] ligneau x1, lin j, vanni-mercier g, jouvet m, muir jl, ganellin cr, stark h, elz s, schunack w, schwartz j. neurochemical and behavioral effects of ciproxifan, a potent histamine h3-receptor antagonist. j pharmacol exp ther. 1998 nov; 287(2):658-66.

3874-54-2
184025-18-1
Synthesis of Ciproxifan from 4-Chloro-4'-fluorobutyrophenone

Ciproxifan Suppliers

Global( 60)Suppliers
Supplier Tel Email Country ProdList Advantage
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29322 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10523 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
ShenZhen Trendseen Biological Technology Co.,Ltd.
13417589054 trendseenbio@gmail.com China 11681 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43348 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
Shanghai Boyle Chemical Co., Ltd. sales@boylechem.com China 2923 55

View Lastest Price from Ciproxifan manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
	Ciproxifan pictures 2019-12-24 Ciproxifan
184025-18-1
US $1.00 / g 1g 99% 20kg Career Henan Chemical Co
  • 	Ciproxifan pictures
  • Ciproxifan
    184025-18-1
  • US $1.00 / g
  • 99%
  • Career Henan Chemical Co
Cyclopropyl[4-[3-(1H-imidazol-5-yl)propoxy]phenyl]methanone FUB 359 Methanone, cyclopropyl[4-[3-(1H-iMidazol-4-yl)propoxy]phenyl]- Ciproxifan, >=99% CS-757 Ciproxifan (FUB-359) Methanone, cyclopropyl[4-[3-(1H-imidazol-5-yl)propoxy]phenyl]- Ciproxifan USP/EP/BP 184025-18-1 Inhibitors