Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C16H25NO3.ClH |
| Molecular Weight | 315.836 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C)C1=C(OCCN(C)C)C=C(C)C(OC(C)=O)=C1
InChI
InChIKey=IPWGSXZCDPTDEH-UHFFFAOYSA-N
InChI=1S/C16H25NO3.ClH/c1-11(2)14-10-15(20-13(4)18)12(3)9-16(14)19-8-7-17(5)6;/h9-11H,7-8H2,1-6H3;1H
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C16H25NO3 |
| Molecular Weight | 279.3746 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/9711459Curator's Comment: description was created based on several sources, including
https://books.google.ru/books?id=S4GJio79XOUC&pg=PA97&lpg=PA97&dq=MOXISYLYTE+%09Withdrawal&source=bl&ots=dzBbL_E8c0&sig=r1pfUZ1LhFGihzzNswfGr7f38Mg&hl=ru&sa=X&ved=0ahUKEwjNlJeazZnOAhWJnBoKHZRoC3YQ6AEIVzAJ#v=onepage&q=MOXISYLYTE%20%09Withdrawal&f=false
http://www.ncbi.nlm.nih.gov/pubmed/1475074
Sources: http://www.ncbi.nlm.nih.gov/pubmed/9711459
Curator's Comment: description was created based on several sources, including
https://books.google.ru/books?id=S4GJio79XOUC&pg=PA97&lpg=PA97&dq=MOXISYLYTE+%09Withdrawal&source=bl&ots=dzBbL_E8c0&sig=r1pfUZ1LhFGihzzNswfGr7f38Mg&hl=ru&sa=X&ved=0ahUKEwjNlJeazZnOAhWJnBoKHZRoC3YQ6AEIVzAJ#v=onepage&q=MOXISYLYTE%20%09Withdrawal&f=false
http://www.ncbi.nlm.nih.gov/pubmed/1475074
Moxisylyte, also known as thymoxamine, is a drug used in urology for the treatment of erectile dysfunction, also was studied, that this drug may be useful to treat ocular disorders such as diabetic retinopathy. It is an alpha1-adrenergic antagonist. Was developed for self-injection therapy in France and marketed in several European countries as Icavex. In the spring 2005 the manufacturer of Icavex decided to withdraw this drug from Europe market, presumable due to its low market shares.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2094251 Sources: http://www.ncbi.nlm.nih.gov/pubmed/10699651 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Effects of adrenergic agents on the expression of zebrafish (Danio rerio) vitellogenin Ao1. | 2009-07-01 |
|
| Raynaud's phenomenon (primary). | 2008-12-16 |
|
| Noradrenergic control of GnRH release from the ewe hypothalamus in vitro: sensitivity to oestradiol. | 2008-12 |
|
| Raynaud's phenomenon (secondary). | 2008-09-26 |
|
| Oral vasodilators for primary Raynaud's phenomenon. | 2008-04-16 |
|
| Noradrenergic control of arginine vasopressin release from the ewe hypothalamus in vitro: sensitivity to oestradiol. | 2008-04 |
|
| Electroacupuncture-induced pressor and chronotropic effects in anesthetized rats. | 2006-01-30 |
|
| Unoprostone isopropyl ester darkens iris color in pigmented rabbits with sympathetic denervation. | 2003-08 |
|
| Alpha(1L)-, but not alpha(1H)-, adrenoceptor antagonist prevents allergic bronchoconstriction in guinea pigs in vivo. | 2002-09-27 |
|
| Assessment of the intrinsic urethral sphincter component function in postprostatectomy urinary incontinence. | 2002 |
|
| The esterase-like activity of serum albumin may be due to cholinesterase contamination. | 2001-10 |
|
| Synergistic effects of sildenafil on relaxation of rabbit and rat cavernosal smooth muscles when combined with various vasoactive agents. | 2001-10 |
|
| [Intracavernous injections in the treatment of erectile dysfunction in spinal cord injured patients: experience with 36 patients]. | 2001-02 |
|
| Are alpha-blockers involved in lower urinary tract dysfunction in multiple system atrophy? A comparison of prazosin and moxisylyte. | 2000-03-15 |
|
| Ergotamine-induced peripheral ischaemia reversed by oral thymoxamine hydrochloride. | 1986-01 |
|
| Effects of thymoxamine and its metabolites on clonidine-induced hypotension and bradycardia in rats. | 1982-07 |
|
| Effect of thymoxamine and pilocarpine on the depth of the anterior chamber. | 1980-10 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/9711459
Intracavernous injection of moxisylyte at 10, 20 or 30 mg can induce an erection adequate for intercourse in most of the patients
Route of Administration:
Other
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/2522580
Moxisylyte hydrochloride on isolated human penile corpus cavernosum tissue was investigated and compared with other alpha-adrenergic antagonists. Moxisylyte produced a concentration-dependent relaxation of a norepinephrine-induced (1 x 10(-5) M) contraction of the corpus cavernosum tissue. Pretreatment with 1 x 10(-6) M doses of moxisylyte reduced competitively the norepinephrine-induced contraction
| Substance Class |
Chemical
Created
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admin
on
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Mon Mar 31 17:48:10 GMT 2025
by
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| Record UNII |
WK2KZM9V6X
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Validated (UNII)
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NCI_THESAURUS |
C29713
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FDA ORPHAN DRUG |
19887
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m7648
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964-52-3
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13758
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C87585
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170448
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235778
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100000088303
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ACTIVE MOIETY |