106685-40-9 Usage
Naphthoic acid derivative
Adapalene, a new class of drugs Naphthoic acid derivatives, was developed by France Galdeama Laboratories Company. It first entered into market in June 1996, under the trade name "Differin", mainly used for relieving inflammatory skin lesions, adjusting differentiation of hair follicles, gland epithelial cells, and also acne treatment.
Pharmacological effects
Adapalene is a retinoid compounds, and is proven to have anti-inflammatory properties in both in vivo and in vitro models of inflammation. It has stable chemical structure, and is not easily to break down in the air and the light. It shares the same mode of action with retinoic acid, bounding to specific retinoic acid nuclear receptors except that adapalene doesn’t bound to the cytoplasmic protein binding receptor. It has been proven to treat acne and affect acne vulgaris and differentiation in skin drug tests established by mouse animal model. Its mechanism of action is reducing the formation of micro-acne through leading the normal differentiation of hair follicle cells. In the standard anti-inflammatory assay both in vivo and in vitro, adapalene has a better effect than retinoic acid. It can inhibit the chemotaxis reaction of human polymorphonuclear leukocytes and also inhibit the metabolism of polymorphonuclear cell through inhibition the formation of anti-inflammatory mediators via oxidation reaction of arachidonic acid, thus relieving inflammatory response by the cell-mediated response. It is useful in the treatment of routine skin with acne, pimples and pustules as the main performance. It can also be used for the treatment of the acne presented in face, chest and back.
The above information is edited by the lookchem of Dai Xiongfeng.
Pharmacokinetics
The transdermal absorption rate of adapalene is very low. In clinical trials, the adapalene level of skin acne areas subject to long-term treatment is undetectable. Appling C14 labeled adapalene for rats (intravenous, intraperitoneal injection, oral and dermal medication), rabbits (intravenous oral and dermal administration), respectively, clarified the distribution of radioactivity among various tissues. Also, liver, spleen adrenal and ovarian have the highest level. Adapalene is mainly metabolized through demethylation, hydroxylation and binding reactions of oxygen 1 and metabolism in vivo and mainly excreted through bile.
[Interaction] No interaction between the product and other skin drugs has been reported. But we should not use other retinoids or other drugs with similar mechanism of action. Adapalene has stable chemical structure, and is not easily to break down in the air and sunlight. A wide range of animal and human studies found no phototoxicity and photosensitivity. However, it is not clear whether it is safe to take it when animal and humans are subject to repeated exposure to sunlight or ultraviolet. Avoid excessive sunshine and UV radiation when use this product. Adapalene has a very low level of transdermal absorption, making it impossible to interact with the systematic medication drugs. No evidence was found that the effect of birth control pills, antibiotics and other oral medications are affected by the using Duff Man for treating skin disease.
Duff Man may have a slight local stimulation. Being treated together with the peeling agent, agent or contraction irritating substances can cause additional irritation. Therefore, use other skin medication early in the morning such as erythromycin (concentrations ≤4%), clindamycin phosphate (1%) aqueous solution or benzoyl peroxide gel (concentration ≤10%); Use Duff Man gel at night so that you can avoid drug co-degradation or accumulation of stimulation effect.
[Adverse reactions] During the first 2-4 weeks of treatment, the most common adverse reactions are erythema, dryness, scaling, itching, burning or tingling. The extent is mostly mild to moderate. Less frequent adverse reactions include: sunburn, skin irritation, burning and stinging skin discomfort. Rarely adverse reactions include: redness of acne, dermatitis and contact dermatitis, eye swelling, conjunctivitis, redness, itching, skin discoloration, rashes and eczema. Reduce the amount of drugs applied or totally withdrawal when serious adverse reactions happen.
Adapalene acid drug safety compared with other topical Vitamin A
The effect of traditional topical Vitamin A acid drugs (RA) on the treatment of acne vulgaris is indeed very good, but the irritating side effects limit its use. RA causes local irritation because of its unstable structure and poor receptor selectivity caused by series of weak divalent bond chains in its molecular structure. Studies have shown that RA can be degraded by a number of factors: exposure to sunlight within 24 h, 60.0%~80.0% of baseline concentration RA degradation, and if use an oxidizing agent such as benzoyl peroxide the same time when apply RA, 80% of RA would be degraded within 4 h, and all RA disappear within 24 h. In order to find a more stable molecule with similar effect as RA but much smaller side effect, people developed a naphthoic acid derivative-adapalene. Adapalene has small irritation effect due to: 1. Molecularly stable: The unstable divalent bond chains in RA are replaced by the aromatic ring of naphthoic acid, making it stable in the light and oxidants without degradation even in 72 h. 2. Highly selective receptor binding: after entering the cell, RA first bound to cytoplasmic vitamin A acid bound protein (CRABP), and has no selectivity when binds to nuclear receptor RARα, β, γ. Adapalene does not bind CRABP, but selectively binds to specific amino acids sequences of the binding site in nuclear receptor RAR-β and RAR-γ receptor, then binds to RXR, further binds to specific DNA sites, regulating transcription machinery, protein synthesis, and cell proliferation and differentiation. Therefore, it is highly specific and has a small side effect. 3. Low cellular toxicity: Study found that effects of different vitamin A acid on keratinocyte cell cytotoxicity are also different. Adapalene molecule is neutral, has low cytotoxicity to keratinocytes compared with the long-chain organic acids, Vitamin A acid. 4. Adapalene has a clear anti-inflammatory effect. However, this kind of effect for other Vitamin A acid is not still clear.
In short, adapalene, a third generation vitamin A drugs, not only have a stronger effect on regulation of epidermal cell differentiation, inhibit proliferation of hair follicle keratinocytes and keratinocytes, inhibition sebaceous cell proliferation, dissolved angle plug acne, etc than all-trans vitamin A acid drugs, but also has a strong anti-inflammatory effect. Because of its unique stability, its efficacy and tolerability is much higher than other Vitamin A acid drugs.
Uses
Different sources of media describe the Uses of 106685-40-9 differently. You can refer to the following data:
1. Retinoic acid analogs. Adapalene is an agonist of RARβ, and RARγ receptor. Adapalene inhibits cell proliferation and inducing apoptosis in colorectal cancer cells in vitro. Adapalene gel is an effective medication for treatment of acne.
2. Adapalene has been used as a retinoic acid receptor (RAR) agonist to study its effects on inhibiting transcription of hepatitis B virus in covalently closed circular DNA (cccDNA). It has also been used as a component to culture mixed lymphocyte reactions (MLR) to study its effects on isolated macrophages.
3. Retinoid selective for retinoic acid receptor (RAR) subtypes ?and . Antiacne
4. Retinoid selective for retinoic acid receptor (RAR) subtypes β and γ. Antiacne.
5. anesthetic
6. inhibits serotonin and noradrenaline reuptake antidepressant antimigraine therapeutic
7. Acnetreatment
Description
Adapalene is a synthetic retinoid and an agonist of retinoic acid receptors (RARs; Kds = 1,100, 34, and 130 nM for RARα, RARβ, and RARγ, respectively). It inhibits growth and differentiation of sebocytes in a concentration-dependent manner in primary rat preputial cell culture. Adapalene (10 μM) completely inhibits the activity of soybean 15-lipoxygenase (15-LOX) in an enzyme assay and inhibits the 5- and 15-LOX pathways in human blood polymorphonuclear leukocytes (PMNs). It reduces the protein levels of toll-like receptor 2 (TLR2) and IL-10 in skin explants isolated from patients with acne and healthy controls in a concentration-dependent manner but increases the expression of the antigen-presenting protein CD1d in acne skin explants while decreasing it in control explants. It inhibits inflammation in rodent models of ear edema induced by arachidonic acid and carrageenan-induced paw edema. Adapalene (100 μM) also induces apoptosis and inhibits proliferation of CC-531, HT-29, and LoVo colon cancer cells and reduces tumor growth in a DLD-1 colon cancer nude mouse xenograft model in a dose-dependent manner. Formulations containing adapalene have been used in the treatment of acne vulgaris.
Chemical Properties
White Crystalline Solid
Originator
Adaferin ,Laboratoires Galderma ,France
Definition
ChEBI: A naphthoic acid that is CD437 in which the phenolic hydroxy group has been converted to its methyl ether.
Indications
Adapalene (Differin) is a polyaromatic retinoidlike
compound that binds to specific retinoic acid nuclear receptors
and is thought to normalize the differentiation
of keratinocytes in the sebaceous acroinfundibulum.
Adapelene is indicated for topical treatment of acne.
Minor local irritation is a common, usually tolerable
side effect. In contrast to other drugs of the retinoid
group, adapalene has not been shown to be teratogenic
in rodents. However, since adequate human studies are
lacking, its use in pregnant women should be discouraged
until further information is available.
Manufacturing Process
Preparation of 6-(3-(1-adamantyl)-4-methoxyphenyl)-2-naphthoic acid consist
of 4 steps.
1. 2-(1-Adamantyl)-4-bromophenol.
34.6 g (200 mmol) of p-bromophenol and 30.4 g (200 mmol) of 1-
adamantanol are dissolved in 100 ml of dichloromethane. To the resulting
solution there are slowly added 10 ml of concentrated sulfuric acid. The
mixture is stirred for 8 hours at ambient temperature, poured into water,
neutralized with sodium bicarbonate, extracted with methylehe chloride, dried
and evaporated. After recrystallization in isooctane 52.8 g of the expected
product are obtained. Yield - 86%. MP: 140°-141°C.
2. 2-(1-Adamantyl)-4-bromoanisole.
To suspension of sodium hydride (80% in oil, 4.32 g, 144 mmol) in 50 ml of
THF, there are slowly added while maintaining the temperature at 20°C, 36.8
g (120 mmol) of 2-(1-adamantyl)-4-bromophenol. The mixture is stirred for 1
hour at ambient temperature at which point 9 ml of methyl iodide are added.
The mixture is then stirred for 2 hours at 20°C, poured into water, extracted
with ether, dried and evaporated. The product is purified by passage through a
silica column (10x30), eluting with a mixture of hexane (90%) and
dichloromethane (10%). On evaporation, 26.2 g of a white solid are obtained.
Yield - 68%. MP: 138°-139°C.
3. Methyl ester of 6-(3-(1-adamantyl)-4-methoxyphenyl)-2-naphthoic acid.
To a suspension of magnesium (1.64 g, 67.5 mmol in 30 ml of THF, there is
added a solution of 1.4 g (4.5 mmol) of 2-(1-adamantyl)-4-bromoanisole and
0.39 ml of dibromoethane in 10 ml of THF. The mixture is stirred until the
reaction is initiated and then there is slowly added a solution of (40.8 mmol)
of 2-(1-adamantyl)-4-bromoanisole in 90 ml of THF. The mixture is refluxed
for 2 hours, and then cooled to 20°C. After that 6.2 g (45 mmol) of
anhydrous ZnCl2 are added. The mixture is stirred for 1 hour at 20°C at which
point 7.95 g (30 mmol) of methyl 6-bromo-2-naphthoate are added followed
by addition of 300 g of NiCl2/1,2-(diphenylphosphino)ethane-complex as the
catalyst. The mixture is stirred again for 2 hours at 20°C, poured into water,
extracted with CH2Cl2 dried and evaporated. The product is isolated by column chromatography, eluting with a mixture of heptane (70%) and
dichloromethane (30%) and then recrystallized in ethyl acetate. 12.2 g of the
expected product are obtained. Yield - 78%. MP: 222°-223°C.
4. 6-(3-(1-Adamantyl)-4-methoxyphenyl)-2-naphthoic acid.
10.5 g of the ester obtained above (step 3) are treated with a solution of soda
in methanol (200 ml, 4.2 N). The mixture is heated at reflux for 48 hours. The
solvents are evaporated and the resulting residue is taken up in water and
acidified with concentrated HCl. The solid is filtered and dried under vacuum
over phosphoric anhydride. The resulting white solid is recrystallized in a
mixture of THF and ethyl acetate. 8.2 g of expected product are obtained.
Yield - 81%. MP: 325°-327°C.
Brand name
Differin (Galderma).
Therapeutic Function
Antiacne
General Description
Adapalene is a third-generation synthetic retinoid and a highly lipophilic compound derived from naphthoic acid. It is widely used in the treatment of acne.
Biological Activity
Retinoic acid analog that is a RAR β and RAR γ agonist (AC 50 values are 2.2, 9.3, 22 and > 1000 nM for RAR β , RAR γ , RAR α and RXR α receptors respectively). Inhibits proliferation and induces apoptosis in colorectal cancer cell in vitro . Displays comedolytic activity.
Biochem/physiol Actions
Retinoic acid analogue that is a RARβ and RARγ agonist (AC50 values are 2.2, 9.3, 22 and > 1000 nM for RARβ, RARγ, RARα and RXRα receptors respectively). Inhibits proliferation and induces apoptosis in colorectal cancer cells in vitro. Displays comedolytic activity. Its unique pharmacological properties make it superior to other retinoids for the treatment of acne.
Structure and conformation
Retinoid-like compound that binds to retinoic acid nuclear receptors,
but not to cytoplasmic receptor proteins.
References
1) Michel et al. (1998), Pharmacology of Adapalene; Br. J. Dermatol., 139 Suppl. 52 3
2) Ocker et al. (2003), The synthetic retinoid adapalene inhibits proliferation and induces apoptosis in colorectal cancer cells on vitro; Int. J. Cancer, 107 453
3) Milikan et al. (2000), Adapalene: an update on newer comparative studies between the various retinoids; Int. J. Dermatol., 39 784
4) Bernard et al. (1993), Adapalene, a new chemical entity with retinoid activity; Skin Pharmacol., 6 61
Check Digit Verification of cas no
The CAS Registry Mumber 106685-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,8 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106685-40:
(8*1)+(7*0)+(6*6)+(5*6)+(4*8)+(3*5)+(2*4)+(1*0)=129
129 % 10 = 9
So 106685-40-9 is a valid CAS Registry Number.
InChI:InChI=1/C28H28O3/c1-31-26-7-6-23(21-2-3-22-12-24(27(29)30)5-4-20(22)11-21)13-25(26)28-14-17-8-18(15-28)10-19(9-17)16-28/h2-7,11-13,17-19H,8-10,14-16H2,1H3,(H,29,30)
106685-40-9Relevant articles and documents
Integration of borylation of aryllithiums and Suzuki-Miyaura coupling using monolithic Pd catalyst
Nagaki,Hirose,Moriwaki,Mitamura,Matsukawa,Ishizuka,Yoshida
, p. 4690 - 4694 (2016)
Integration of the preparation of arylboronic esters via aryllithiums and Suzuki-Miyaura coupling using monolithic Pd catalyst without an intentionally added base was achieved. A continuous operation has been done successfully for over 21 hours.
Preparation method of adapalene
-
, (2020/07/12)
The invention discloses a preparation method of adapalene. According to the preparation method of adapalene, 2-methoxycarbonyl-6-naphthol p-toluenesulfonate and 4-methoxyphenylboronic acid which are low in price and easy to obtain are used as raw materials and bis (triphenylphosphine) nickel chloride is used as a catalyst, Suzuki coupling is performed to obtain 6-(4-methoxyphenyl)-2-methyl naphthoate, then alkylation reaction with 1-adamantanol is made to obtain 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-methyl naphthoate, and finally ester hydrolysis is performed to obtain the target product adapalene. The method is simple in process, raw materials are available, the yield is high and the cost is low, and the quality can reach a satisfactory level.
Room Temperature Deoxyfluorination of Benzaldehydes and α-Ketoesters with Sulfuryl Fluoride and Tetramethylammonium Fluoride
Melvin, Patrick R.,Ferguson, Devin M.,Schimler, Sydonie D.,Bland, Douglas C.,Sanford, Melanie S.
supporting information, p. 1350 - 1353 (2019/03/08)
A method for the room temperature deoxyfluorination of benzaldehydes and α-ketoesters using sulfuryl fluoride and Me4NF is described. A large scope of aryl and heteroaryl substrates is demonstrated, and this method compares favorably to other common deoxyfluorination methods for many substrates.
