ChemicalBook >> CAS DataBase List >>Tafluprost

Tafluprost

CAS No.
209860-87-7
Chemical Name:
Tafluprost
Synonyms
aflupros;TafL;MK2452;uprost;AFP-168;TAFLUPROST;Tafluprosttrade;Tafluprost USP/EP/BP;209860-87-7 Tafluprost;He has fluprostaglandin
CBNumber:
CB3401660
Molecular Formula:
C25H34F2O5
Molecular Weight:
452.53
MDL Number:
MFCD08062150
MOL File:
209860-87-7.mol
MSDS File:
SDS
Last updated:2024-04-07 18:44:46

Tafluprost Properties

Boiling point 552.9±50.0 °C(Predicted)
Density 1.186
storage temp. 2-8°C
solubility soluble in Chloroform, DMSO, Ethyl Acetate
form Clear, colorless to slightly yellow oil
pka 14.48±0.70(Predicted)
FDA UNII 1O6WQ6T7G3
ATC code S01EE05

SAFETY

Risk and Safety Statements

Tafluprost price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 10005440 Tafluprost ≥98% 209860-87-7 1mg $112 2024-03-01 Buy
Cayman Chemical 10005440 Tafluprost ≥98% 209860-87-7 5mg $499 2024-03-01 Buy
Cayman Chemical 10005440 Tafluprost ≥98% 209860-87-7 10mg $884 2024-03-01 Buy
Cayman Chemical 10005440 Tafluprost ≥98% 209860-87-7 25mg $1381 2024-03-01 Buy
Tocris 6427 Tafluprost ≥95%(HPLC) 209860-87-7 5 $245 2021-12-16 Buy
Product number Packaging Price Buy
10005440 1mg $112 Buy
10005440 5mg $499 Buy
10005440 10mg $884 Buy
10005440 25mg $1381 Buy
6427 5 $245 Buy

Tafluprost Chemical Properties,Uses,Production

Description

Glaucoma is second only to cataracts as a causative factor of blindness. By 2010, it is estimated that approximately 60 million people worldwide will be afflicted by glaucoma, so effective treatments should garner a large market. PG analogs have been widely used for lowering IOP by increasing uveoscleral outflow through agonism of the prostanoid FP receptor, and currently marketed versions include latanoprost, unoprostone isopropyl ester, bimatoprost, and travoprost. Compared to the carboxylic acid of latanaprost (Ki=4.7 nM), the carboxylic acid of tafluprost displayed a 10-fold greater affinity for the prostanoid FP receptor (Ki=0.4 nM). The synthesis of tafluprost begins with a Wittig condensation of the protected bicyclic lactone carbaldehyde with a dimethyl phosphonate ketone derivative.
Compared to the carboxylic acid of latanaprost (Ki 4.7 nM), the carboxylic acid of tafluprost displayed a 10-fold greater affinity for the prostanoid FP receptor (Ki 0.4 nM). The synthesis of tafluprost begins with a Wittig condensation of the protected bicyclic lactone carbaldehyde with a dimethyl phosphonate ketone derivative. The bottom appendage is then completed by the fluorination of the ketone with morpholino-sulfur trifluoride. Hydrolysis of the benzoate ester protecting group liberates the hydroxy group, and reduction of the lactone is accomplished with aluminum hydride to generate the lactol. Condensation of this intermediate with the phosphonium salt of the acid side chain generates the free acid, or active ingredient, which is subsequently esterified with 2-iodopropane in the presence of DBU. .

Originator

Santen/Asahi Glass (Japan)

Uses

Tafluprost is a novel prostanoid used in the treatment of glaucoma and is the first prostanoid to be released in a preservative free-formula.

Definition

ChEBI: Tafluprost is a prostaglandin Falpha that is prostaglandin F2alpha in which the carboxylic acid function has been converted to the corresponding isopropyl ester and the 3-hydroxy-1-octenyl side-chain is substituted by 3,3-difluoro-4-phenoxybut-1-enyl. Used for treatment of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension. It has a role as a prostaglandin receptor agonist. It is a prostaglandins Falpha, an organofluorine compound and an isopropyl ester. It is functionally related to a prostaglandin F2alpha.

brand name

Taflotan

Synthesis

The synthesis was initiated from the Corey aldehyde 131. Horner-Emmons condensation of the bicyclic carbaldehyde 131 with the dimethyl phosphonate 132 using NaH in DMF gave enone 133 in 90% yield. Fluorination of the enone 133 was accomplished upon reaction with morpholino-sulfur trifluoride (134) in chloroform to yield the corresponding difluorinated compound 135. Hydrolysis of the benzoate ester group of 135 with K2CO3 in methanol at room temperature afforded alcohol 136 in 71% yield from 133. Reduction of the lactone group of 136 with diisobutyl aluminum hydride (DIBAL) in THF/toluene gave lactol 137 in 83% yield. Lactol 137 was condensed with the phosphonium ylide prepared by deprotonation of phosphonium salt 138 with sodium bis(trimethylsilyl)amide (NaHMDS) in THF/toluene to give the prostaglandin F2-alpha derivative 139 in excellent Z/E selectivity (99:1). The synthesis was completed by esterification of compound 139 with isopropyl iodide and DBU in acetone to provide tafluprost (XVIII) in 72% yield.

Synthesis_209860-87-7

Mode of action

Tafluprost(209860-87-7) is a Prostaglandin Analog. The mechanism of action of tafluprost is as a Prostaglandin Receptor Agonist. It is believed that prostanoid FP-receptor agonists such as tafluprost reduce IOP by increasing the uveoscleral outflow of aqueous humor. There is some evidence that tafluprost may lower IOP by interaction with the EP3 receptor.
DB08819

Tafluprost Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 258)Suppliers
Supplier Tel Email Country ProdList Advantage
airuikechemical co., ltd.
+undefined86-15315557071 sales02@airuikechemical.com China 994 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21695 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9353 55
Shanghai finete Pharmaceutical Co., Ltd.
+86-18221039705 CHINA 139 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3620 58
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Zhejiang ZETian Fine Chemicals Co. LTD
18957127338 stella@zetchem.com China 2141 58
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 967 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58

View Lastest Price from Tafluprost manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Tafluprost pictures 2024-04-10 Tafluprost
209860-87-7
US $0.00 / Kg/Bag 2Kg/Bag 99% up, High Density 20 tons Sinoway Industrial co., ltd.
Tafluprost pictures 2024-04-07 Tafluprost
209860-87-7
US $0.00-0.00 / g 1g 99.9% 20tons airuikechemical co., ltd.
Tafluprost pictures 2023-03-12 Tafluprost
209860-87-7
US $0.00 / kg 1kg 98.0%min 100kg LY Global chemicals co.,ltd .
  • Tafluprost pictures
  • Tafluprost
    209860-87-7
  • US $0.00 / Kg/Bag
  • 99% up, High Density
  • Sinoway Industrial co., ltd.
  • Tafluprost pictures
  • Tafluprost
    209860-87-7
  • US $0.00-0.00 / g
  • 99.9%
  • airuikechemical co., ltd.
  • Tafluprost pictures
  • Tafluprost
    209860-87-7
  • US $0.00 / kg
  • 98.0%min
  • LY Global chemicals co.,ltd .

Tafluprost Spectrum

TAFLUPROST (5Z)-7-[(1R,2R,3R,5S)-2-[(1E)-3,3-Difluoro-4-phenoxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-5-heptenoic acid 1-methylethyl ester 15,15-DIFLUORO-9ALPHA,11ALPHA-DIHYDROXY-16-PHENOXY-17,18,19,20-TETRANOR-PROSTA-5Z,13E-DIEN-1-OIC ACID, ISOPROPYL ESTER AFP-168 Tafluprost5-Heptenoic acid, 7-[(1R,2R,3R,5S)-2-[(1E)-3,3-difluoro-4-phenoxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-,1-methylethyl ester, (5Z)- He has fluprostaglandin MK2452 TafL uprost 5-Heptenoic acid, 7-[(1R,2R,3R,5S)-2-[(1E)-3,3-difluoro-4-phenoxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-, 1-methylethyl ester, (5Z)- Tafluprost USP/EP/BP (Z)-Isopropyl 7-((1R,2R,3R,5S)-2-((E)-3,3-difluoro-4-phenoxybut-1-en-1-yl)-3,5-dihydroxycyclopentyl)hept-5-enoate TafluprostQ: What is Tafluprost Q: What is the CAS Number of Tafluprost Q: What is the storage condition of Tafluprost Q: What are the applications of Tafluprost 209860-87-7 Tafluprost aflupros Tafluprosttrade Isopropyl (Z)-7-[(1R,2R,3R,5S)-2-[(E)-3,3-Difluoro-4-phenoxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-5-heptenoate 209860-87-7 09860-87-7 C25H34F2O5