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Ripasudil hydrochloride dihydrate

Product Name
Ripasudil hydrochloride dihydrate
CAS No.
887375-67-9
Chemical Name
Ripasudil hydrochloride dihydrate
Synonyms
K-115 HCL;K 115; K115;K115 HCL 2H2O;K-115 (HCl H2O);Ripasudil (K-115);K115 HCl Dihydrate;Ripasudil free base;K 155 HCl dihydrate;RipasudilHCl Hydrate;Ripasudil HCl Dihydrate
CBNumber
CB52667596
Molecular Formula
C15H21ClFN3O3S
Formula Weight
377.86
MOL File
887375-67-9.mol
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Ripasudil hydrochloride dihydrate Property

storage temp. 
Store at -20°C
solubility 
insoluble in EtOH; ≥123.2 mg/mL in DMSO; ≥41.7 mg/mL in H2O
form 
solid
color 
White to off-white
Stability:
Hygroscopic
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Safety

Risk Statements 
24/25-26-28
Safety Statements 
28-38-41-48
HS Code 
29339900
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
R517900
Product name
RipasudilHydrochloride
Packaging
100mg
Price
$1815
Updated
2021/12/16
ChemScene
Product number
CS-3401
Product name
Ripasudil
Purity
99.75%
Packaging
100mg
Price
$1920
Updated
2021/12/16
ChemScene
Product number
CS-3401
Product name
Ripasudil
Purity
99.75%
Packaging
50mg
Price
$1188
Updated
2021/12/16
Biosynth Carbosynth
Product number
FR162274
Product name
Ripasudil HCl hydrate
Packaging
2mg
Price
$125
Updated
2021/12/16
ApexBio Technology
Product number
B4809
Product name
K-115
Packaging
5mg
Price
$135
Updated
2021/12/16
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Ripasudil hydrochloride dihydrate Chemical Properties,Usage,Production

Description

Ripasudil hydrochloride hydrate (Glanatec®) was approved in Japan in 2014 for the treatment of glaucoma and ocular hypertension. Originally discovered by D. Western Therapeutics Institute, Inc. and licensed by the Kowa Company, Ltd, ripasudil functions as a selective Rho-kinase inhibitor and reduces intraocular pressure by stimulation of aqueous humour drainage of the trabecular meshwork. While this recent approval allows for use of ripasudil as a twice-daily monotherapy treatment when other drugs cannot be used or are not effective, clinical trials using ripasudil as a combination therapy with other glaucoma drugs have shown promising results in the treatment of primary open-angle glaucoma or ocular hypertension. Currently, the Kowa Company is also pursuing trials focused on the use of ripasudil for the treatment of diabetic retinopathy and diabetic macular edema.

Uses

Ripasudil Hydrochloride Dihydrate is a derivative of fasudil and a rho kinase inhibitor (1,2). It is used for the treatment of glaucoma and ocular hypertension.

Uses

Ripasudil (Glanatec TM, Kowa Pharmaceutical), a close derivative of fasudil, is another Rho kinase inhibitor approved in Japan at the end of 2014 for the treatment of glaucoma and ocular hypertensionwhen other therapeutic agents are not effective or cannot be administered. Additionally, ripasudil has been tested in diabetic retinopathy clinical trials and shown to promote corneal endothelial cell proliferation, endothelium regeneration, and wound healing.

Synthesis

While initial synthetic routes to ripasudil were carried out via a stepwise functionalization of 4-fluoroisoquinoline-5-sulfonyl chloride (238), more recent reports describe an efficient route to ripasudil employing a late stage-coupling of Boc-diazepane (237) with 4-fluoroisoquinoline-5-sulfonyl chloride (238), enabling synthesis on multi-kilogram scale and isolation of the drug in high purity. This optimized route to ripasudil begins with 2-nitrobenzene sulfonyl chloride (NsCl)- mediated protection of (S)-2-amino-1-propanol (234) in 82% yield. In this case, use of the NaHCO3/THF/H2O conditions were essential for preventing bis-nosylation.228 Alcohol activation with methanesulfonyl chloride (MsCl) in N-methyl morpholine (NMM) took place smoothly to give the corresponding mesylate 235 in 91% yield. Direct mesylate displacement with 3-aminopropanol and subsequent amine protection as the carbamate ((Boc)2O) in a one-pot fashion provided the corresponding Boc-amino propanol product 236 in 95% yield over 2 steps. With the acyclic diazepane precursor 236 in hand, employment of the intramolecular Fukuyama-Mitsunobu N-alkyl cyclization conditions (diisopropyl azodicarboxylate (DIAD)/PPh3) allowed generation of the diazepane in 75% yield. Nosyl group cleavage with thiophenol/K2CO3 provided the Boc-diazepane 237 in 65% overall yield and 98% purity following a pH-controlled aqueous workup. Finally, 4-fluoroisoquinoline- 5-sulfonyl chloride (238)?aprepared via subjection of 4- fluoroisoquinoline (239) to sulfur trioxide and sulfuric acid followed by treatment with thionyl chloride and finally 4 N HCl in ethyl acetate?awas involved in a 1-pot, two-step procedure in which this sulfonyl chloride was coupled with diazepane 237 (TEA/MeCN) to access the ripasudil framework in quantitative yield. Synthesis of the final drug target by deprotection with 4 M HCl in ethyl acetate followed by neutralization with aqueous sodium hydroxide provided the free base of ripasudil in 93% yield and 99.8% purity. Conversion to the more stable hydrochloride dihydrate form could be performed by treatment of the free base with 1 M HCl/EtOH and subsequent heating of the hydrochloride in H2O/acetone to provide ripasudil hydrochloride dihydrate XXIX in 83% yield.

in vivo

in optic nerve crush (nc) c57bl/6 mice model, oral administration of k-115 (1 mg/kg/d) increased 34 ± 3% survival of rgcs after nc [2].

References

shimokawa h, takeshita a. rho-kinase is an important therapeutic target in cardiovascular medicine[j]. arteriosclerosis, thrombosis, and vascular biology, 2005, 25(9): 1767-1775.yamamoto k, maruyama k, himori n, et al. the novel rho kinase (rock) inhibitor k-115: a new candidate drug for neuroprotective treatment in glaucomanovel rho kinase inhibitor[j]. investigative ophthalmology & visual science, 2014, 55(11): 7126-7136.tanihara h, inoue t, yamamoto t, et al. phase 1

Ripasudil hydrochloride dihydrate Preparation Products And Raw materials

Raw materials

Preparation Products

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Ripasudil hydrochloride dihydrate Suppliers

Chemvon Biotechnology Co., Ltd
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021-50790412
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+86-21-50790419
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China
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Dalian Meilun Biotech Co., Ltd.
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0411-62910999 13889544652
Email
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Country
China
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Shanghai Topbiochem Technology Co., Ltd
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021-58170097
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info@topbiochem.com
Country
China
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Haoyuan Chemexpress Co., Ltd.
Tel
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China
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UHN Shanghai Research & Development Co., Ltd.
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+86 (21) 5895-8628
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MedChemexpress LLC
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Hygeia (Chengdu) pharmaceutical technique Co., Ltd
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Suzhou Haiheng Biological Pharmaceutical Co., Ltd.
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SPIRO PHARMA
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Pharmacodia (Beijing) Co.,Ltd
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887375-67-9, Ripasudil hydrochloride dihydrateRelated Search:


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