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CAS RN: 145040-37-5 | Product Number: C2635
Candesartan Cilexetil
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Purity: >98.0%(T)(HPLC)
Synonyms:
Product Documents:
| Size | Unit Price | Belgium | Japan* | Quantity |
|---|---|---|---|---|
| 200MG |
36,00 €
|
Contact Us | ≥40 |
|
| 1G |
122,00 €
|
2 | 19 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
| Product Number | C2635 |
| Purity / Analysis Method | >98.0%(T)(HPLC) |
| Molecular Formula / Molecular Weight | C__3__3H__3__4N__6O__6 = 610.67 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Refrigerated (0-10°C) |
| Condition to Avoid | Heat Sensitive |
| CAS RN | 145040-37-5 |
| Reaxys Registry Number | 7328188 |
| PubChem Substance ID | 160871141 |
| Merck Index (14) | 1739 |
| MDL Number | MFCD00871371 |
Specifications
| Appearance | White to Almost white powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(Nonaqueous Titration) | min. 98.0 % |
| Melting point | 157.0 to 163.0 °C |
Properties (reference)
| Melting Point | 159 °C |
| Maximum Absorption Wavelength | 304(EtOH) nm |
| Solubility (slightly sol. in) | Methanol |
GHS
| Pictogram |
|
| Signal Word | Danger |
| Hazard Statements | H360 : May damage fertility or the unborn child. H362 : May cause harm to breast-fed children. |
| Precautionary Statements | P263 : Avoid contact during pregnancy and while nursing. P260 : Do not breathe dust. P202 : Do not handle until all safety precautions have been read and understood. P201 : Obtain special instructions before use. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection. P308 + P313 : IF exposed or concerned: Get medical advice/ attention. |
Related Laws:
| RTECS# | DD6672500 |
Transport Information:
| HS Number | 2933998090 |
Application
Candesartan Cilexetili: A Selective AT1 Subtype Angiotensin II Receptor Antagonist
Candesartan cilexetili, a prodrug, is hydrolyzed to candesartan during absorption from the gastrointestinal tract. The active metabolite, candesartan, acts as a selective AT1 subtype angiotensin II receptor antagonist.
Angiotensin II is formed from angiotensin I in a reaction catalyzed by angiotensin-converting enzyme (ACE). Angiotensin II can activate two different receptors, AT1 and AT2, both of which are coupled to G-protein. Angiotensin II is the principal pressor agent of the renin-angiotensin system, and the actions of it are mediate through AT1 receptors. Candesartan has much greater affinity for the AT1 receptor than for the AT2 receptor, and blocks of the AT1 receptor in many tissues by an antagonist suppressed the action of angiotensin II. Candesartan exerts a long-lasting antihypertensive action in spontaneously hypertensive rats. For your reference, [M2797] is a synthetic intermediate of candesartan cilexetili. (The product is for research purpose only.)
Angiotensin II is formed from angiotensin I in a reaction catalyzed by angiotensin-converting enzyme (ACE). Angiotensin II can activate two different receptors, AT1 and AT2, both of which are coupled to G-protein. Angiotensin II is the principal pressor agent of the renin-angiotensin system, and the actions of it are mediate through AT1 receptors. Candesartan has much greater affinity for the AT1 receptor than for the AT2 receptor, and blocks of the AT1 receptor in many tissues by an antagonist suppressed the action of angiotensin II. Candesartan exerts a long-lasting antihypertensive action in spontaneously hypertensive rats. For your reference, [M2797] is a synthetic intermediate of candesartan cilexetili. (The product is for research purpose only.)
References
- Protective effects of candesartan cilexetil (TCV-116) against stroke, kidney dysfunction and cardiac hypertrophy in stroke-prone spontaneously hypertensive rats
- Beneficial effects of candesartan, an angiotensin II type 1 receptor blocker, on beta-cell function and morphology in db/db mice
- The angiotensin II receptor antagonist candesartan cilexetil (TCV-116) ameliorates retinal disorders in rats
PubMed Literature
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