Showing posts with label Steroids. Show all posts
Showing posts with label Steroids. Show all posts

Bilocarbine.. Uses and salts in medicine to stimulate sweat and ophthalmology and to make preparations against hair loss

Bilocarbine:

Bilocarbine, also known as pilocarpine, is a naturally occurring alkaloid found in the leaves of several plants, particularly Jaborandi. It's a potent cholinergic agonist, meaning it mimics the effects of the neurotransmitter acetylcholine in the body. This property gives it a wide range of medical applications, including:

Ophthalmology:

- Glaucoma treatment:

Bilocarbine is primarily used to treat glaucoma, a condition characterized by increased pressure in the eye that can damage the optic nerve. It works by stimulating the ciliary muscle in the eye, which contracts and improves the flow of aqueous humor, the fluid that fills the eye and helps regulate pressure.

- Miosis (pupil constriction):

Bilocarbine can also be used to constrict the pupil, which can be helpful in certain eye conditions like uveitis (inflammation of the uveal tract) or after surgery.

Sweating:

- Treatment of anhidrosis (lack of sweating):

Bilocarbine can be used to stimulate sweating in people with anhidrosis, a condition that can be caused by various factors like nerve damage, diabetes, or certain medications. This can help regulate body temperature and prevent heatstroke.

- Diagnosis of cystic fibrosis:

Bilocarbine is sometimes used in sweat tests to diagnose cystic fibrosis, a genetic condition that affects the lungs and digestive system.

Other uses:

- Xerostomia (dry mouth):

Bilocarbine can be used to stimulate saliva production in people with xerostomia, a condition often caused by medications or radiation therapy.

- Alopecia (hair loss):

Bilocarbine has been studied as a potential treatment for alopecia, but there is limited evidence to support its effectiveness.

Bilocarbine salts:

Bilocarbine is typically used in the form of salts, which are more soluble and easier to administer than the free base. Some common bilocarbine salts used in medicine include:

- Pilocarpine hydrochloride:

This is the most common salt of bilocarbine and is available in various forms, including eye drops, pills, and injections.

- Pilocarpine nitrate:

This salt is less common than pilocarpine hydrochloride but may be preferred for some patients due to its different side effect profile.

Side Effects:

It's important to note that bilocarbine can have side effects, including:
  • Blurred vision.
  • Eye pain.
  • Headache.
  • Nausea and vomiting.
  • Increased sweating.
  • Diarrhea.
  • Urinary urgency and frequency.
Before using bilocarbine, it's crucial to consult with a healthcare professional to discuss the potential risks and benefits and determine if it's the right treatment for you.

Prostaglandins are the most important arachronic acid derivatives .. Prostadyl. Prostaglandins. Alpha Prostol. Telspruit. Prostalin. Dinoprost

Prostaglandins arachronic acid derivatives:


  • Prostadyl (DCI) or (INN) (Prostaglandins E1), a crystalline precostagenin, a biological extract. Used as a holding material. It is also used as a stimulant to release arthroputin from the renal cortex and inhibits blood clots.
  • alpha-Prostol (DCI) or (INN) is a synthetic prostaglandins used to treat the fertility of female horse (Persians).
  • Telsproset (DCI) or (INN) isotopes of prostaglandins with one atom of oxygen and one carbon atom replaced with one nitrogen seed and one sulfur atom with annular structure.
This group includes synthetic products such as Prostalin (DCI), INN, DINOPROST (DCI) or INN, which retain the infrastructure of natural products and have similar physiological activity.


Prostaglandins:

Prostaglandins are a group of substances of a lipid nature derived from the fatty acids of 20 carbons (eicosanoids), which contain a cyclopentane ring and constitute a family of cellular mediators, with diverse, often conflicting effects. Prostaglandins affect and act on different systems of the organism, including the nervous system, the smooth tissue, the blood and the reproductive system; they play an important role in regulating various functions such as blood pressure, blood coagulation, the allergic inflammatory response and the activity of the digestive system.

prostate gland:

The name prostaglandin comes from the prostate gland. When the prostaglandins were first isolated in the seminal fluid in 1935, it was thought to be part of the secretions of the prostate. In 1971, it was discovered that acetylsalicylic acid (aspirin) and its derivatives can inhibit the synthesis of prostaglandins. The biochemists Sune Karl Bergström, Bengt Samuelsson and John Robert Vane received the Nobel Prize in Physiology and Medicine in 1982 for their research on prostaglandins.

essential fatty acids:

They are synthesized from essential fatty acids by the action of different enzymes such as cyclooxygenases, lipoxygenases, cytochrome P-450, peroxidases, etc. Cyclooxygenase gives rise to prostaglandins, thromboxane A-II and prostacyclin (PGI2); lipoxygenase gives rise to the acids HPETEs, HETE and leukotrienes; cytochrome P-450 generates HETEs and hepóxidos (EETs). The pathway through which arachidonic acid is metabolized to eicosanoids depends on the tissue, the phospholipase A2, the stimulus, the presence of endogenous and pharmacological inducers or inhibitors, etc.

The role of prostaglandins::

Prostaglandins must exert their effect on the cells of origin and adjacent, acting as autocrine and paracrine hormones, being destroyed in the lungs. The actions are multiple and some have practical utility, such as PGE1, which is used clinically to keep the ductus arteriosus open, in children with congenital heart disease (alprostadil) and for the treatment or prevention of gastroduodenal ulcer (misoprostol). PGE2 (dinoprostone) is used as oxytocin in the induction of labor, the expulsion of the dead fetus and the treatment of hydatidiform mole or spontaneous abortion.

Prostaglandin Functions:

The functions of prostaglandins can be summarized in five points:
  • Involved in the inflammatory response: vasodilation, increased permeability of the tissues allowing the passage of leukocytes, platelet antiaggregant, stimulation of nerve endings of pain, etc.
  • Increase in the secretion of gastric mucus, and decrease in gastric acid secretion.
  • They cause the contraction of the smooth muscles. This is especially important in the woman's uterus. In the human semen there are small amounts of prostaglandins to favor the contraction of the uterus and as a consequence the ascension of the spermatozoa to the uterine tubes (fallopian tubes). In the same way, they are released during menstruation, to favor the detachment of the endometrium. Thus, menstrual pains are often treated with inhibitors of the release of prostaglandins.
  • Intervene in the regulation of body temperature.
  • Control the decrease in blood pressure by promoting the elimination of substances in the kidney.

Cocaine.. Of the leaves of Erythroxylum coca

- Cocaine:
Extracted from the leaves of some types of coca, especially from the "Erythroxylum coca", also occurs synthetically.
Commercial cocaine (raw cocaine) is not pure but contains 80% to 94% of cocaine, but is still included in this item. Pure cocaine is a saline and its water solution gives alkaline reaction, gives cocaine many salts, and is a highly effective anesthetic.

What is cocaine?
Cocaine is a stimulant and addictive drug made from the leaves of the coca plant, native to South America. While doctors can use it for legitimate medicinal purposes - such as local anesthesia in some surgical operations, for example - recreational cocaine use is illegal. Cocaine sold on the street looks like a fine white crystallized powder. Street vendors often mix it with substances such as cornstarch, talcum powder or flour to increase their profits. They can also be mixed with other drugs such as amphetamine (a stimulant) or with synthetic opioids, including fentanyl. Adding synthetic opioids to cocaine is particularly risky when the person who uses the drug does not know that it contains other dangerous substances. The increasing number of deaths from cocaine overdose could be due to this alteration of the drug.
Common names of cocaine include coca, crack, lady, stone, snow and Snow White, among others; In English it is called:
- blow
- coke
- crack
- rock
- snow.

Amino acid derivatives.. levothyroxine. Leoserinen. Razironin. Thyroxine

Amino acid derivatives:
1 - levothyroxen (DCI) or (INN) and thyroxine DL (3-D4) 4- hyroxy-3,5-diiodophenoxy (3,5-diiodophenyl) alanine or 3,5,3,5-tetraiodothyrinin).
Thyroxine is extracted from the thyroid or obtained synthetically. It is an amino-aromatic acid; it is white or yellowish-branched, with no solubility in water or any normal solvent, which increases the basic metabolic rate and oxygen consumption. It affects the thymbocyte, controls the action of proteins and fats and affects any deficiency of iodine in organisms and is used to treat thyroid gland disease as well as loss of thyroid secretion or disorder. It is effectively in the isomer's habitat. Sodium salt is white powder, low in water with similar activity.
2-lyseronin (DCI) or (INN) and rasironin (DCI) or (INN) (DL-3,5,3-triiodothyronine) (3) 4- (4- hydroxyl-3-iodophenoxy) 3,5-diiodophenyl ] alanine). Tri-dutheronine is also extracted from the thyroid gland; it has more physiological activity than zeroxin.

Amino acids are the basic units of proteins. It is recalled that the proteins are formed of numerous amino acids linked together by a peptide bond.
An amino acid contains an acid function and has an amine function. There are also w-amino acids where the acid and amine functions are 1,2- or 1,3-.

Hydrophobic amino acids:
Aliphatic - Glycine (gly, G), Alanine (Ala, A), Valine (val, V), Leucine (leu, L), Isoleucine (Ile, I).
Aromatic - Phenylalanine (phe, E), Tryptophan (trp, W).
Thioether - Methionine (met, M).
Secondary amines - Proline (pro, P), Hydroxyproline (Hyp).

Hydrophilic amino acids:
Polar - Alcohols - Serine (ser, S), Threonine (thr, T) - Thiols - Cysteine ​​(cys, C) - Phenol - Tyrosine (tyr, Y) - Amides - Asparagine (asn, N), Glutamine (gln, Q) ).
Cationic - Lysine (lily, K), Arginine (arg, R), Histidine (his, H).
Anionics - Aspartate (asp, D) Glutamate (glue, E).

W-amino acids:
b -alanine G -aminobutyric acid, b -aminoisobutyric acid.

General properties:
General physicochemical properties:
Solubility:
Amino acids are very soluble in water due to their amphionic character.
R-CH (NH2) -COOH = R-CH (NH3 +) - COO-
Their solubility varies all the same according to the radical R and the pH.

Optical properties:
Absorption spectra:
In aqueous solution, only amino acids having an aromatic radical absorb.
Phenylalanine l max = 254 nm
Tyrosine and tryptophan l max = 280 nm

Rotating power:
If R ¹ H, the carbon a is asymmetric.
Amino acids therefore exist in the form of two enantiomers: L-amino acid D-amino acid.
All natural amino acids are of the L series, just as all sugars are of the D series.
Some amino acids have two asymmetric carbons (threonine, isoleucine). The presence of two asymmetric carbons implies the existence of four diastereoisomers.
Rotatory power: Amino acids are optically active.

Acid-base properties:
In amino acids, the amine group is known to be basic and the carboxylic group to be acidic.
There are therefore two successive acid-base equilibria:
KA1 KA2
R-CH (NH3 +) - COOH = R-CH (NH3 +) - COO- = R-CH (NH2) -COO-
Generally pKA1 »2 and pKA2» 9

Colchicine. Colchicum plants are formed in the form of ammonia blocks, crystals, powders or toxic yellow flakes

- Colchicine:
It is found in plants of the type of "Kulchikum Atomnal" and is in the form of blocks of glue or crystals or powders or yellow flakes are very toxic; used in medicine.

For what conditions or diseases is this medication prescribed?
Colchicine is used to prevent gout attacks (sudden and severe pain in one or more joints, caused by abnormally high levels of a substance called uric acid in the blood) in adults. Colchicine (Colcrys) is also used to relieve the pain of gout attacks when they occur. Colchicine (Colcrys) is also used to treat familial Mediterranean fever (FMF; an innate condition that causes episodes of fever, pain and swelling of the stomach area, lungs and joints in adults and children over 4 years of age. Colchicine It is not a pain reliever and cannot be used to treat pain that is not caused by gout or FMF. Colchicine belongs to a class of medications called anti-gout agents. It works by stopping the natural processes that cause inflammation and other symptoms of gout and FMF

How should this medicine be used?
The presentation of colchicine is in a tablet and solution (liquid; Gloperba) to take by mouth, with or without food. When colchicine is used to prevent gout attacks or to treat FMF, it is usually taken once or twice a day. When colchicine (Colcrys) is used to relieve the pain of a gout attack, a dose is usually taken at the first sign of pain and a smaller second dose is usually taken an hour later. If you do not experience relief or have another attack several days after treatment, talk to your doctor before taking additional doses of the medication. Follow the instructions on the label of your prescription carefully and ask your doctor or pharmacist to explain any part you do not understand. Take colchicine exactly as directed. Do not take a greater or lesser amount of the medicine, or take it more often than your doctor's prescription indicates.
It is important to use an oral syringe (measuring device) to accurately measure the correct amount of fluid for each dose; Do not use a house spoon.
If you are taking colchicine (Colcrys) to treat FMF, your doctor may start with a low dose and gradually increase it. Your doctor may decrease your dose if you experience side effects.
If you are taking colchicine to prevent gout attacks, call your doctor immediately if you experience a gout attack during your treatment. Your doctor may tell you to take an additional dose of colchicine, followed by a smaller dose one hour later. If you take additional doses of colchicine to treat a gout attack, you should not take the next scheduled dose of colchicine until at least 12 hours have elapsed since you took the additional doses.
Colchicine can prevent gout attacks and control FMF only while taking the medication. Continue to take colchicine even if you feel well. Do not stop taking colchicine without talking to your doctor.

What other uses does this medication have?
This medicine may be prescribed for other uses. Ask your doctor or pharmacist for more information.

What special precautions should I follow?
Before taking colchicine,
- tell the doctor and pharmacist if you are allergic to colchicine, any other medicine or any of the ingredients in the tablets or colchicine solution. Ask your doctor or pharmacist or check the medication guide for a list of ingredients.
- Tell your doctor and pharmacist about what other prescription and non-prescription medications, vitamins and nutritional supplements you are taking, have taken during the last 14 days or plan to take. Be sure to mention any of the following: antibiotics such as azithromycin (Zithromax), clarithromycin (Biaxin), erythromycin (E.E.S., E-Mycin); telithromycin (Ketek; not available in the U.S.); antifungal medications such as fluconazole (Diflucan), itraconazole (Sporanox), ketoconazole (Nizoral), and posaconazole (Noxafil); aprepitant (Emend); certain cholesterol-lowering medications (statins) such as atorvastatin (Lipitor), fluvastatin (Lescol), lovastatin (Mevacor), pravastatin (Pravachol), and simvastatin (Zocor); cyclosporine (Gengraf, Neoral, Sandimmune); digoxin (Digitek, Lanoxin); diltiazem (Cardizem, Dilacor, Tiazac, others); fibrates such as bezafibrate, fenofibrate (Antara, Lipofen), and gemfibrozil (Lopid); HIV or AIDS medications such as amprenavir (Agenerase), atazanavir (Reyataz), fosamprenavir (Lexiva), indinavir (Crixivan), nelfinavir (Viracept), ritonavir (in Kaletra, Norvir), and saquinavir (Invirase); nefazodone; ranolazine (Ranexa); and Verapamil (Calan, Covera, Isoptin, Verelan). Your doctor may need to change the doses of your medications or monitor you closely to see if you have side effects. Many other medications may also interact with colchicine, so be sure to tell your doctor about all the medications you are taking, even those that do not appear on this list.
- Tell your doctor if you have or have had liver disease. Your doctor will probably tell you not to take colchicine if you are taking any other medications or if you have kidney and liver disease.
- Tell your doctor if you are pregnant, plan to become pregnant or are breastfeeding. If you become pregnant while taking colchicine, call your doctor.

What special diet should I follow while I take this medicine?
Do not eat grapefruit or drink grapefruit juice during your colchicine treatment.

What do I have to do if I forget to take a dose?
Take the missed dose as soon as you remember. If you are taking colchicine on a regular basis and it is almost time for the next dose, skip the dose you did not take and continue with your regular dosing schedule. Do not double the dose to make up for the missed dose.
However, if you are taking colchicine (Colcrys) to treat a gout attack that occurred while taking colchicine to prevent gout attacks and forgot to take the second dose, take the missed dose as soon as you remember. Then, wait at least 12 hours before taking your next scheduled dose of colchicine.

What are the side effects that this medicine could cause?
Colchicine may cause side effects. Tell your doctor if any of the following symptoms are severe or do not go away:
nausea
- vomiting
- diarrhea
- stomach pain or cramps
Some Side Effects Can Be Serious. If you experience any of the following symptoms, stop taking colchicine and call your doctor immediately:
- muscle pain or weakness
- numbness or tingling in the fingers or toes
- unusual bleeding or bruising
- sore throat, fever, chills or other symptoms of infection
- tiredness or weakness
- pale or gray color of the lips, tongue or palms
Colchicine may decrease fertility in men. Talk to your doctor about the risks of taking colchicine.

How should I store or dispose of this medicine?
Keep this medicine in its original container, tightly closed and out of the reach of children. Store it at room temperature and away from excess heat and moisture (do not store it in the bathroom).
It is important that you keep all medications out of the sight and reach of children, because many containers (such as weekly pill boxes, and those containing ophthalmic drops, creams, patches and inhalers) are not proof of small children, who can easily open them. In order to protect them from intoxication, always wear safety covers and immediately place medications in a safe place, one that is up and away from your sight and reach. http://www.upandaway.org/es/
Medications that are no longer needed should be disposed of in an appropriate manner to ensure that pets, children and others cannot consume them. However, you should not discard these medications by the toilet. Instead, the best way to get rid of your medications is through a medication return program. Talk to your pharmacist or contact your local trash / recycling department to learn about your community's drug return programs. See the Food and Drug Administration (FDA) website (https://goo.gl/xRXbPn) for more information on how to safely dispose of medications if you do not have access to the medication return program.

what should I do in case of an overdose?
In case of overdose, go immediately to the nearest hospital emergency room. Taking too much colchicine can cause death.
Symptoms of overdose may include:
- stomach ache
nausea
- vomiting
- diarrhea
- unusual bleeding or bruising
- sore throat, fever, chills or other symptoms of infection
- pale or gray color of the lips, tongue or palms
slow breathing
- slow or stopped heartbeat

What other important information should I know?
Attend all appointments with your doctor and the laboratory. Your doctor may order some laboratory tests to check your response to colchicine.
Do not let anyone else use your medicine. Ask your pharmacist any questions you have about refilling your prescription.
It is important that you keep a written list of all the medications you are taking, including those you received with a prescription and those you bought without a prescription, including vitamins and diet supplements. You should have the list every time you visit your doctor or when you are admitted to a hospital. It is also important information in emergencies.

Thrombocyan and lecotrains are laxative to prostoglandins and are created or installed in cells of arachidonic acid

Thrombocene and lecotrains are prostaglandins and are created or installed in cells of arachidonic acid.
Although their functions correspond to the functions of the prostrogendins and their similarity to the structure, they do not contain the basic structure of brosinok.
Thermoboxanas can be derived from prostaglandins by synthesis and biochemistry.
It causes the accumulation of blood clots and contractions of the arteries and is considered an important organization for the work of polyunsaturated fatty acids.
Lycotriins are called because they are present in the white globules and in their triangular structure.
It is an effective holding of pulmonary people and plays an important role in allergic reactions.
A: Thromboxan B2: It is a blood vessel and pulmonary people, and it is used to collect blood clots.
L-cotraine C4: It is 100 to 1000 times more effective than histamine or prostaglandins for its effect on airway passage in the pulmonary artery.
Other hormones
Hormones, which differ in structure from the hormones referred to above, such as melatonin, found in the cone or coniferous gland, can be considered as endol derivatives.

Prostaglandins are metabolites of arachidonic acid, obtained from membrane phospholipids by the action of phospholipases (several existing subtypes). Liposoluble molecules intended for secretion in the extracellular medium, these are cytokines that play important roles in living organisms. Indeed, prostaglandins are paracrine and autocrine signaling agents that activate many GPCRs (membrane-bound 7-segment membrane receptors coupled to G proteins). Each prostaglandin has 20 carbon atoms including a ring with 5 carbon atoms. They are chemical mediators that have various physiological effects, contributing in particular to the development of several inflammatory manifestations, vasodilatation and pain.
Prostaglandins belong to the class of prostanoids, which also contains thromboxanes and prostacyclins. Prostanoids are themselves a sub-category of eicosanoids (combining prostanoids and leukotrienes).

History and nomenclature:
The name prostaglandin (PG) comes from prostate. Prostaglandin was first isolated in seminal fluid in 1935 by Swedish physiologist Ulf von Euler1 and independently by W.W. Goldblatt2. It was believed that it was secreted by the prostate (in fact the prostaglandins are produced by the seminal vesicles). It has been shown later that several other tissues produce prostaglandins which have varied effects.
In nomenclature, we denote PG the series - E, F, Alpha or I - the class - 1,2 or 3 - followed by isomerism if it is necessary - Trans or Cis.

Biochemistry:
Prostaglandins are found in virtually all tissues and organs. They are autocrine and paracrine lipid mediators that act on platelets, endothelium, uterus and mast cells, among other things. They are synthesized in the cell from essential fatty acids:
- di-homo-gamma-linolenic acid (C20: 3 (n-6)) leads to the prostaglandins of the index series.
arachidonic acid (AA, C20: 4 (n-6)) gives the prostaglandins of the index series.
- Eicosapentaenoic acid (EPA, C20: 5 (n-3)) leads to the prostaglandins of the index series.
The production of prostaglandins of the index series requires arachidonic acid. It can be provided by the diet, but is also produced endogenously by the body, by phospholipase A2 degradation of phosphatidylcholine molecules (a membrane phospholipid). Arachidonic acid then undergoes the action of cyclooxygenase or that of lipoxygenase. Cyclooxygenase will lead to the formation of thromboxane, prostacyclin (also called prostaglandin I2) and prostaglandins D, E and F. Lipoxygenase is active in leucocytes and macrophages and forms leukotrienes.

Antibiotics. Streptomycin. Chloramphenicol. Erythromycin

- Penicillin and its derivatives with penicillin acid structure; salts of these products
- Streptomycin and its derivatives; salts of these products
- Tetracycline and its derivatives; salts of these products
- chloramphenicol and its derivatives; salts of these products
- erythromycin and its derivatives; salts of these products

Antibiotics such as toocamycin. Daihydrocodine. Niacomorphine. Oxymoron. Hydrocodone. Hydromorph

Plant alkalis, natural or synthetically produced, their salts, ethers, esters, other derivatives thereof.
- alkaloids of opium and their derivatives; salts of these products:
(INN), Hydromoron (INN), Morphine, Necomorphine (INN), Oxycodon (INN), Oximorfon (INN), Pigeon Forge, (INN), Vulkoden (INN), Thepakon (INN), Thebayen; salts of these products.

Natural or synthetically produced glycosides, and their salts - rotoside and its derivatives

Glycosides are mainly present in the Kingdom of Lebanon. It is usually taken by acids, bases and enzymes on a glycemic part and a non-glycemic part. These parts are connected to each other through a carbon atom of sugar. Thus, in vitro products such as (faxinin) and (hamamlatin) of heading 29.40 are not considered glycosides.
The most common types of glycosides that are naturally present are or-relicoxides, in which a part of the sugar and glycone are linked by an acetylcholine function. However, there are naturally occurring glycosides such as n-glycosides, S-glycosides, and C-glycosides, in which the sugary carbon atom is associated with the glycone through a nitrogen atom, a large atom or a carbon atom (eg casimirwedine, Sometimes sugar through an ester group.
They are generally solid, colorless compounds that make up preservatives in plant organisms or act as stimulants for body functions.

Glycosides, digitalis, lannata. Borioria - Digoxin and Digitonin

Digitalis Glycosides are found in plants of repressive species (such as Dr. Lannata, D. Purioria), some of which are used in medicine as a heart enhancer, and are included in this group: Digitoxin, a very odorless white crystalline powder, Digitonin are two digitalis soap and are used as chemical reagents.

Antihypertensive anti-thrombolytic agents, anti-tumor drugs such as Atacobinemast, insulin inhibitor

6. Thromo antagonists such as lecotrains and lecotrains, which are classified according to their composition (eg, serratrost (INN) (item 29.18) and montalocast (INN).
7- Anticonvulsants such as Atacobinemast (INN).
8. Drugs of 30.03 and 30.04, especially insulin inhibitors (zinc insulin, insulin of protamine, gluten insulin, zinc insulin, globin, insulin - histone).

Products have a hormonal effect but have no similar structure. Hicks Estrol. Diethyl stylosterol. Clombinin

A-Dai Enistrol (INN) (3,4 bis bisque (hydroxyl phenyl) hexa - 2,4 dyne) (item 29.07).
B) Hicks ether (INN) (3.4 bis bisque) (4-hydroxene phenylhexane) (heading 29.07).
(Item 29.7), methylated ether (derived from it) (heading 29.09), and propionate derivatives derived from it (heading 29.09), hydroxyphylene (hex-3-in) (Item 29.15) and figurines derived therefrom (heading 29.32).
D. Clombenin (INN) (anti-estrogen), heading 29.22.
H. Tamokinin (INN) (anti-estrogen) Item: 29.22.
G - endothelin is an antagonist such as, Drentin (INN) (item 29.33), ATRsantan (INN) (Item: 29.34) Cetazantan (INN) (item: 29.35).