General Description
Yellow to light-orange crystalline powder.
Reactivity Profile
ALL-TRANS-RETINOIC ACID(302-79-4) may discolor on exposure to light. ALL-TRANS-RETINOIC ACID(302-79-4) is extremely sensitive to exposure to light and, therefore, ALL-TRANS-RETINOIC ACID(302-79-4) should be fully protected from light during all handling. Solutions are unstable in the presence of strong oxidizers. This compound is incompatible with strong oxidizing agents. .
Air & Water Reactions
ALL-TRANS-RETINOIC ACID may be sensitive to prolonged exposure to air. Insoluble in water.
Fire Hazard
Flash point data for this chemical are not available; however, ALL-TRANS-RETINOIC ACID is probably combustible.
Description
all-
trans Retinoic acid is a metabolite of vitamin A and a ligand for retinoic acid receptors (RARs) with IC
50 values of 9, 3, and 10 nM for RARα, RARβ, and RARγ, respectively, in radioligand binding assays.
1 It induces expression of a luciferase reporter in COS-7 cells expressing RARα, RARβ, or RARγ (EC
50s = 169, 9, and 2 nM, respectively). all-
trans Retinoic acid (17 nmol) reduces papilloma formation induced by phorbol 12-myristate 13-acetate (TPA; Item No.
10008014) in mice.
2 It reduces bile duct proliferation, hydroxyproline levels, and liver inflammation in a rat model of α-naphthylisothiocyanate-induced chronic cholestasis and reduces plasma levels of alkaline phosphatase and bile salts in the
Mdr2-/- mouse model of cholestasis.
3 all-
trans Retinoic acid also reduces hepatic fat accumulation, triglycerides, body weight, and serum glucose levels in mice with Western diet-induced obesity.
4
Chemical Properties
Yellow-Orange Powder
Originator
Aberel,McNeil,US,1973
Definition
ChEBI: Retinoic acid(302-79-4) is a retinoid in which all four exocyclic double bonds have E- (trans-) geometry. It is a naturally occurring derivative of vitamin A (retinol). Retinoids such as tretinoin are important regulators of cell reproduction, proliferation, and differentiation and are used to treat acne and photodamaged skin and to manage keratinization disorders such as ichthyosis and keratosis follicularis.
Indications
Topical tretinoin (Retin-A, Renova, Avita), like isotretinoin,
alters keratinization in the acroinfundibulum.
In addition, it reverses certain premalignant and other
histological changes associated with the photoaging
changes that accompany chronic exposure to ultraviolet
radiation. Topically applied tretinoin is indicated in
comedogenic and papulopustular acne vulgaris, and its
mild exfoliative effects make it sometimes useful in molluscum
contagiosum, flat warts, and some ichthyotic disorders.
It is often prescribed to lessen the clinical signs of
photoaging (wrinkling and hyperpigmented macules).
Manufacturing Process
100 parts of beta-ionol are dissolved in 200 parts of dimethylforrnamide and
after the addition of 165 parts of triphenylphosphine hydrobromide, stirred for 7 hours at room temperature. Then 70 parts of 4-methyl-1-al-hexadiene-
(2,4)-acid-(6) (melting point 177°C, white needles from water) are added to
the now clear solution. 150 parts of isopropanol are added and the whole
cooled to -30°C. Into this solution, while stirring vigorously, 190 parts by
volume of a 30% solution of sodium methylate in methanol are allowed to
flow in. A vigorous exothermic reaction takes place and the temperature in the
interior of the flask rises to +5°C. It is stirred for another 5 minutes and
neutralized with 10% of sulfuric acid (until acid to Congo).
After stirring for 2 hours at room temperature, the mass of vitamin A acid has
crystallized out. It is sharply filtered off by suction and washed with a little
ice-cold isopropanol. From the filtrate, a further small amount of mainly all
trans vitamin A acid crystallizes out upon the addition of water. The filter cake
is suspended in 600 parts of water and stirred for 4 hours at room
temperature; it is filtered by suction and the product washed with water. It is
dried in vacuo at 40° to 50°C and 115 parts of vitamin A acid are obtained.
The melting point lies between 146° and 159°C.
The mixture of the all trans and mainly 9,10-cis vitamin A acid may be
separated by fractional crystallization from ethanol. All trans vitamin A acid
has a melting point of 180° to 182°C and 9,10-cis vitamin A acid, which
crystallized in the form of pale yellow fine needles collected into clusters, has
a melting point of 189° to 190°C.
Brand name
A-acido;Acid a vit;Acnavit;Acnavyse;Acretin;Airoderm;Aknebon;Aknefug;Anition;Antibio-aberel;Apsor;A-vitamisyre;Avitoin;Cordes vas;Dermoclar;Dermojuventas;Derugin;Locacid;Pigmanorm;R0 22-6595;Reiderma;Retin a;Ro 1-5488;Sebo-psor;Stie vaa;Stievaa;Tretin m;Vas dexa;Verra-med;Vitacid a.
Therapeutic Function
Keratolytic
World Health Organization (WHO)
Tretinoin, a retinol derivative, was introduced in 1973 exclusively
for the topical treatment of severe acne. Preparations of tretinoin are indicated for
topical use only since oral administration has been associated with risk of toxicity
from hypervitaminosis-A and subsequently of teratogenicity.
Biological Activity
Endogenous agonist for retinoic acid receptors. Also positively modulates PPAR δ receptors (K d = 17 nM). Promotes differentiation of embryonic stem cells (ESCs) into adipocytes, neurons and glia in vitro .
Biochem/physiol Actions
all?trans?Retinoic acid (ATRA) is a ligand for both the retinoic acid receptor (RAR) and the retinoid X receptor (RXR). The bound RAR and RXR act as transcription factors that regulate the growth and differentiation of both normal and malignant cells. Cytochromes P450 (CYPs) catalyze the 4-hydroxylation of ATRA. Retinoic acid primes embryonic stem cells to become neurons.
Clinical Use
The major toxic effect of tretinoin is erythema and
irritation of the skin to which it is applied, especially if
the skin is moist.This toxicity often decreases with continued
therapy.
Toxicology
Oral retinoic acid has strong teratogenic effects on experimental animals (including mice, rats, hamsters, rabbits, monkeys, etc.) and humans[2]. Topical application of retinoic acid on the skin has clear embryotoxicity and teratogenicity to the mothers of mice, rats, hamsters and rabbits in the embryo sensitive period, and can cause maternal systemic toxicity. However, retrospective data so far have not found teratogenicity after topical administration of human skin. Retinoids are irritating to the skin. The skin reaction of the above-mentioned experimental animals is significantly heavier than the human reaction, which can cause different degrees of skin irritation, inflammation, redness, erosion, weakening of the stratum corneum barrier, increased drug absorption, and systemic toxicity depending on the drug concentration and the number of times of administration. Although external use on human skin is irritating, it does not have the above-mentioned serious reactions. It may be due to differences in skin structure and sensitivity to retinoic acid stimulation between animals and humans. Therefore, the safety data of local administration of retinoic acid in animals and its predictive significance for clinical drug safety should be carefully evaluated.
Veterinary Drugs and Treatments
Topical tretinoin may be useful in treating localized follicular or hyperkeratotic disorders such as acanthosis nigrans, idiopathic nasal and
footpad hyperkeratosis, callous pyodermas, or chin acne. Tretinoin’s exact mechanism of action is not well understood, but it stimulates
cellular mitotic activity, increases cell turnover, and decreases the cohesiveness of follicular epithelial cells.
Metabolism
Metabolised in the liver by the cytochrome P450 isoenzyme system to form isotretinoin, 4-oxo-transretinoic acid, and 4-oxo-cis-retinoic acid.
Tretinoin is excreted in the bile and the urine.
storage
Store at -20°C, sealed storage, away from moisture and light
Purification Methods
Purify the acid by chromatography on silicic acid columns, and eluting it with a small amount of EtOH in hexane. Also dissolve it in Et2O, wash it with H2O, dry (Na2SO4), evaporate and the solid residue is recrystallised from MeOH (0.53g /3.5mL MeOH to give 0.14g) or EtOH. It also recrystallises from i-PrOH, or as the methyl ester from MeOH. UV in MeOH has max at 351nm ( 45,000). 9-Cis-acid forms yellow needles from EtOH, with m 189-190o, and its UV in MeOH has max at 343nm ( 36,500); the 13-cis-acid forms red-orange plates from i-PrOH with m 174-175o, and UV has max at 345nm ( 39,800). Store it in the dark, in an inert atmosphere, at 0o [Robeson et al. J Am Chem Soc 77 4111 1955]. [Beilstein 9 IV 2387.]
References
1) Allenby (1993), Retinoic acid receptors and retinoid X receptors: interactions with endogenous retinoic acid; Proc. Natl. Acad. Sci. USA, 90 30
2) Dani et . (1997) Differentiation of embryonic stem cells into adipocytes in vitro; J. Cell Sci. 110 1279
3) Hu (2009) Differentiation Of Spinal Motor Neurons From Pluripotent Human Stem Cells; Nat. Protoc., 4 1295
4) Sasai (2002) Generation of dopaminergic neurons from embryonic stem cells J. Neurol., 249 II 41