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Phytomenadione Wiki2Web Clarity Challenge

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Study Guide: Phytomenadione (Vitamin K1): Properties, Applications, and Identification

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Phytomenadione (Vitamin K1): Properties, Applications, and Identification Study Guide

Nomenclature and Chemical Properties

Phytomenadione is the sole chemical name for vitamin K1.

Answer: True

Explanation: Phytomenadione is the specific chemical name for vitamin K1, distinguishing it from other forms of vitamin K.

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Phylloquinone and phytonadione are recognized synonyms for phytomenadione.

Answer: True

Explanation: Phylloquinone is the biochemical name, and phytonadione is a common pharmaceutical name, both referring to phytomenadione (vitamin K1).

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Phytomenadione is a water-soluble vitamin.

Answer: False

Explanation: Phytomenadione is classified as a fat-soluble vitamin, along with vitamins A, D, and E.

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Phytomenadione is chemically derived from 2-methyl-1,4-naphthoquinone.

Answer: True

Explanation: Phytomenadione possesses a chemical structure based on the 2-methyl-1,4-naphthoquinone core.

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The IUPAC nomenclature for phytomenadione signifies its derivation from the 'naphthalene-1,4-dione' structure.

Answer: True

Explanation: The IUPAC name assigned to phytomenadione, 2-methyl-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enyl]naphthalene-1,4-dione, explicitly includes the naphthalene-1,4-dione core.

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The molecular formula for phytomenadione is C31H46O2.

Answer: True

Explanation: The chemical formula representing phytomenadione is C31H46O2.

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Vitamin K1's structure is based on a 2-methyl-1,4-naphthoquinone core with a phytyl substituent.

Answer: True

Explanation: Phylloquinone (Vitamin K1) is structurally characterized by a 2-methyl-1,4-naphthoquinone nucleus attached to a phytyl side chain.

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Phytomenadione is classified as a polycyclic aromatic ketone.

Answer: True

Explanation: Phytomenadione is chemically described as a polycyclic aromatic ketone.

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The molar mass of phytomenadione is approximately 450.707 g/mol.

Answer: True

Explanation: The calculated molar mass of phytomenadione is approximately 450.707 grams per mole.

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Phytomenadione is chemically classified as a fat-soluble vitamin.

Answer: True

Explanation: Phytomenadione belongs to the group of fat-soluble vitamins, which includes vitamins A, D, E, and K.

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Which of the following is NOT a common synonym for phytomenadione?

Answer: Vitamin K2

Explanation: Phytomenadione is commonly known as Vitamin K1 and Phylloquinone. Vitamin K2 refers to a different group of related compounds (menaquinones).

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Chemically, phytomenadione is classified as a:

Answer: Fat-soluble vitamin

Explanation: Phytomenadione is classified as a fat-soluble vitamin, meaning it dissolves in fats and oils and requires dietary fat for optimal absorption.

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What is the calculated molar mass of phytomenadione in grams per mole?

Answer: 450.707 g/mol

Explanation: The calculated molar mass of phytomenadione is approximately 450.707 grams per mole.

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What is the molecular formula representing phytomenadione?

Answer: C31H46O2

Explanation: The chemical formula representing phytomenadione is C31H46O2.

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The IUPAC nomenclature for phytomenadione signifies its derivation from which fundamental chemical structure?

Answer: Naphthalene

Explanation: The IUPAC nomenclature for phytomenadione indicates it is derived from a naphthalene-1,4-dione core structure.

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Biological Roles and Metabolism

Phytomenadione serves as a crucial cofactor for hepatic synthesis of specific blood coagulation factors.

Answer: True

Explanation: Phytomenadione is essential for the liver to synthesize several key blood clotting factors, playing a vital role in hemostasis.

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Edward Doisy and Henrik Dam received the Nobel Prize for their work related to phytomenadione.

Answer: True

Explanation: Edward Doisy and Henrik Dam were awarded the Nobel Prize in Physiology or Medicine for their discoveries concerning vitamin K.

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Phytomenadione was first isolated in the 20th century.

Answer: True

Explanation: Phytomenadione was first isolated in 1939, which falls within the 20th century.

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In plants, phylloquinone is involved in photosynthesis.

Answer: True

Explanation: In plants, phylloquinone plays a crucial role in photosynthesis, specifically acting as an electron acceptor within the electron transport chain of Photosystem I.

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Vitamin K is essential for the synthesis of coagulation factors II, VII, IX, and X in animals.

Answer: True

Explanation: Vitamin K acts as a cofactor for the liver's synthesis of coagulation factors II (prothrombin), VII, IX, and X.

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Phylloquinone is found in higher concentrations in the liver than in the brain.

Answer: True

Explanation: Within animal tissues, phylloquinone is generally found in higher concentrations in the liver, heart, and pancreas, with lower levels present in the brain, kidneys, and lungs.

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The biosynthesis of vitamin K1 in plants starts with the compound chorismate.

Answer: True

Explanation: The biosynthesis of vitamin K1 in plants and cyanobacteria commences with chorismate, a precursor synthesized via the shikimate pathway.

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The conversion of chorismate to vitamin K1 involves fewer than five steps.

Answer: False

Explanation: The biochemical pathway converting chorismate to vitamin K1 comprises nine sequential steps.

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Vitamin K is required for the synthesis of anticoagulant proteins C and S.

Answer: True

Explanation: In addition to coagulation factors, Vitamin K is essential for the synthesis of anticoagulant proteins, specifically protein C and protein S.

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Phytomenadione plays a role in the formation of bone proteins.

Answer: True

Explanation: Vitamin K is also required for the synthesis of certain bone proteins, contributing to skeletal health.

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Phylloquinone is essential for photosynthesis in plants.

Answer: True

Explanation: Phylloquinone plays an indispensable role in plant photosynthesis, functioning within the electron transport chain of Photosystem I.

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What is the primary role of phytomenadione in the body?

Answer: Facilitating the synthesis of key blood clotting factors

Explanation: The principal biological function of phytomenadione in the body is to facilitate the hepatic synthesis of essential blood clotting factors.

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Who were the Nobel Prize recipients for the discovery work related to phytomenadione?

Answer: Edward Doisy and Henrik Dam

Explanation: Edward Doisy and Henrik Dam were jointly awarded the Nobel Prize in Physiology or Medicine for their discoveries concerning vitamin K.

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What is the specific physiological function of phylloquinone (Vitamin K1) within the photosynthetic process of plants?

Answer: Acting as an electron acceptor in Photosystem I

Explanation: In plants, phylloquinone functions as an electron acceptor within the electron transport chain associated with Photosystem I during photosynthesis.

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Which of the following coagulation factors, synthesized in the liver, is dependent on Vitamin K?

Answer: Factor IX (Christmas factor)

Explanation: Vitamin K is a cofactor for the synthesis of coagulation factors II, VII, IX, and X in the liver. Factor IX is one of these Vitamin K-dependent factors.

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In addition to coagulation factors, Vitamin K is essential for the synthesis of which anticoagulant proteins?

Answer: Protein C and Protein S

Explanation: Vitamin K is vital for the synthesis of anticoagulant proteins, specifically protein C and protein S, which help regulate the coagulation cascade.

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Within animal tissues, in which organs are higher concentrations of phylloquinone typically observed?

Answer: Liver and Heart

Explanation: Within animal tissues, phylloquinone is generally found in higher concentrations in the liver, heart, and pancreas, with lower levels present in the brain, kidneys, and lungs.

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The biochemical pathway for the biosynthesis of Vitamin K1 in plants, commencing with chorismate, comprises how many sequential steps?

Answer: 9 steps

Explanation: The biochemical pathway converting chorismate to vitamin K1 comprises nine sequential steps.

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The source mentions that Vitamin K is required for the formation of what type of proteins in addition to clotting factors?

Answer: Bone proteins

Explanation: Vitamin K is also required for the synthesis of certain bone proteins, contributing to skeletal health, in addition to its role in coagulation factors and anticoagulant proteins.

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Which of the following is NOT a function of Vitamin K mentioned in the source?

Answer: Regulation of body temperature

Explanation: The source details Vitamin K's roles in synthesizing coagulation factors, anticoagulant proteins C and S, and bone proteins. Regulation of body temperature is not mentioned.

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What is the primary role of phytomenadione (phylloquinone) in plant photosynthesis?

Answer: Transporting electrons in Photosystem I

Explanation: In plants, phylloquinone functions as an electron acceptor within the electron transport chain associated with Photosystem I during photosynthesis.

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Clinical and Therapeutic Applications

Phytomenadione is primarily used to treat bleeding disorders related to vitamin K deficiency or anticoagulant overdose, not hemophilia.

Answer: True

Explanation: Phytomenadione is utilized in the treatment of bleeding disorders stemming from vitamin K deficiency or warfarin overdose, rather than hemophilia.

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Vitamin K deficiency bleeding in newborns is a condition that phytomenadione can help prevent and treat.

Answer: True

Explanation: Phytomenadione is recommended for both the prevention and treatment of vitamin K deficiency bleeding in newborns, thereby preventing severe neurological damage.

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Phytomenadione is considered safe for use during pregnancy.

Answer: True

Explanation: Phytomenadione is considered safe for use by pregnant individuals and is also likely safe for use while breastfeeding.

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Phytomenadione is approved for treating anticoagulant poisoning in dogs in Canada under the name Hemophyt.

Answer: True

Explanation: In Canada, phytomenadione, marketed as Hemophyt, is approved for the veterinary treatment of anticoagulant poisoning in dogs.

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Phytomenadione is primarily used to treat vitamin C deficiency.

Answer: False

Explanation: Phytomenadione is utilized for vitamin K deficiency and related bleeding disorders, not vitamin C deficiency.

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Phytomenadione is considered safe for use during pregnancy.

Answer: True

Explanation: Phytomenadione is considered safe for use by pregnant individuals and is also likely safe for use while breastfeeding.

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Phytomenadione is primarily used to treat conditions related to vitamin K deficiency.

Answer: True

Explanation: Phytomenadione is utilized in the treatment of bleeding disorders stemming from vitamin K deficiency, warfarin overdose, and obstructive jaundice.

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Intramuscular administration of phytomenadione is used to prevent severe neurological damage in newborns.

Answer: True

Explanation: Phytomenadione is recommended for the prevention of vitamin K deficiency bleeding in newborns, with intramuscular injections being a common practice to safeguard infants against severe neurological damage.

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According to the source, phytomenadione is used to treat bleeding disorders resulting from:

Answer: Warfarin overdose and general vitamin K deficiency

Explanation: Phytomenadione is indicated for treating bleeding disorders caused by warfarin overdose and general vitamin K deficiency, as well as obstructive jaundice.

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What specific veterinary application for phytomenadione is documented in Canada?

Answer: Treatment of anticoagulant poisoning in dogs

Explanation: In Canada, phytomenadione, marketed as Hemophyt, is approved for the veterinary treatment of anticoagulant poisoning in dogs.

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Phytomenadione is considered safe for use during which life stages?

Answer: Pregnancy and breastfeeding

Explanation: Phytomenadione is considered safe for use by pregnant individuals and is also likely safe for use while breastfeeding.

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Administration, Sources, and Stability

Intramuscular injections of phytomenadione typically show effects within two hours.

Answer: True

Explanation: When phytomenadione is administered via injection, its therapeutic effects are generally observed within two hours.

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Oral administration is a recommended method for phytomenadione.

Answer: True

Explanation: Phytomenadione can be administered through various routes, including orally, subcutaneously, intramuscularly, and intravenously.

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Severe allergic reactions to phytomenadione are particularly associated with intravenous administration, especially when large doses are combined with castor oil.

Answer: True

Explanation: Severe allergic reactions to phytomenadione have been reported, particularly with intravenous administration, especially when large doses were given in conjunction with castor oil.

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Green vegetables are a rich source of dietary phytomenadione.

Answer: True

Explanation: Phytomenadione is commonly found in the diet through the consumption of green vegetables, vegetable oils, and certain fruits.

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Vitamin K is highly stable when exposed to air.

Answer: True

Explanation: Vitamin K exhibits notable stability in the presence of air and moisture, though it is susceptible to decomposition when exposed to sunlight.

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Phytomenadione is susceptible to decomposition when exposed to sunlight.

Answer: True

Explanation: Phytomenadione exhibits stability in the presence of air and moisture but is susceptible to decomposition when exposed to sunlight.

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Phytomenadione is susceptible to decomposition when exposed to sunlight.

Answer: True

Explanation: Phytomenadione exhibits stability in the presence of air and moisture but is susceptible to decomposition when exposed to sunlight.

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Which administration route is NOT mentioned as a recommended method for phytomenadione?

Answer: Intradermal injection

Explanation: The recommended administration routes for phytomenadione include oral, subcutaneous, intramuscular, and intravenous injections. Intradermal injection is not typically listed.

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How quickly can the effects of phytomenadione be observed after injection?

Answer: Within two hours

Explanation: When phytomenadione is administered via injection, its therapeutic effects are generally observed within two hours.

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What is a significant risk associated with intravenous administration of large doses of phytomenadione, especially when combined with castor oil?

Answer: Severe allergic reactions

Explanation: Severe allergic reactions to phytomenadione have been reported, particularly with intravenous administration, especially when large doses were given in conjunction with castor oil.

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Which of the following is a common dietary source of phytomenadione?

Answer: Green vegetables

Explanation: Phytomenadione is commonly found in the diet through the consumption of green vegetables, vegetable oils, and certain fruits.

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Identification and Regulatory Information

Phytomenadione is listed on the World Health Organization's List of Essential Medicines.

Answer: True

Explanation: Phytomenadione is recognized for its importance in public health and is included on the World Health Organization's List of Essential Medicines.

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Mephyton is a trade name for phytomenadione.

Answer: True

Explanation: Mephyton is recognized as one of the proprietary trade names under which phytomenadione is marketed.

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Phytomenadione is used in both human and veterinary medicine.

Answer: True

Explanation: Phytomenadione has distinct ATC codes for human use (B02BA01) and veterinary use (QB02BA01), indicating its application in both fields.

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Phytomenadione requires a prescription in both Canada and the United States.

Answer: True

Explanation: In both Canada and the United States, phytomenadione is classified as a prescription-only medication.

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The CAS Registry Number for phytomenadione is 84-80-0.

Answer: True

Explanation: The Chemical Abstracts Service (CAS) Registry Number uniquely identifying phytomenadione is 84-80-0.

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Phytomenadione is identified by the DrugBank identifier DB01022.

Answer: True

Explanation: Phytomenadione is listed in the DrugBank database under the identifier DB01022.

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The KEGG identifier for phytomenadione is D00148.

Answer: True

Explanation: Phytomenadione is identified in the Kyoto Encyclopedia of Genes and Genomes (KEGG) database with the code D00148.

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The ChEBI identifier for phytomenadione is CHEBI:18067.

Answer: True

Explanation: The Chemical Entities of Biological Interest (ChEBI) identifier assigned to phytomenadione is CHEBI:18067.

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The '#' symbol in the navboxes typically indicates inclusion on the WHO Model List of Essential Medicines.

Answer: True

Explanation: In the context of navigational boxes (navboxes), the '#' symbol generally denotes inclusion on the WHO Model List of Essential Medicines.

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The PubChem Compound ID for phytomenadione is 5284607.

Answer: True

Explanation: The PubChem Compound Identifier (CID) assigned to phytomenadione is 5284607.

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The navboxes link to articles concerning anticoagulants and vitamins.

Answer: True

Explanation: The navigational boxes (navboxes) link to related articles on both vitamins and antihemorrhagic agents, facilitating exploration of interconnected topics.

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What information does the 'Spoken Wikipedia' section provide regarding the article's content?

Answer: False

Explanation: The 'Spoken Wikipedia' section indicates the availability of an audio recording for the article, often specifying the revision date and providing links for access, rather than direct download links.

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Menadione (K3) is listed as a form of Vitamin K under 'Antihemorrhagics (B02)'.

Answer: True

Explanation: Menadione (Vitamin K3) is classified under the ATC code B02, which pertains to antihemorrhagics, indicating its relevance in treating bleeding disorders.

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The UNII identifier for phytomenadione is S5Z3U87QHF.

Answer: True

Explanation: The FDA's Unique Ingredient Identifier (UNII) assigned to phytomenadione is S5Z3U87QHF.

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Phytomenadione is classified as a prescription-only medication in the United States.

Answer: True

Explanation: In the United States, phytomenadione is classified as a prescription-only medication.

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The ChemSpider identifier for phytomenadione is 4447652.

Answer: True

Explanation: The ChemSpider identifier assigned to phytomenadione is 4447652.

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The ECHA InfoCard number for phytomenadione is 100.001.422.

Answer: True

Explanation: The European Chemicals Agency (ECHA) InfoCard number for phytomenadione is 100.001.422.

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Phytomenadione is recognized by which international health organization as an essential medicine?

Answer: The World Health Organization (WHO)

Explanation: Phytomenadione is included on the World Health Organization's List of Essential Medicines, signifying its importance in global healthcare.

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Which of the following is listed as a trade name for phytomenadione?

Answer: Hemophyt

Explanation: Hemophyt is cited as a proprietary trade name for phytomenadione, particularly in veterinary applications in Canada.

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Phytomenadione is classified as a prescription-only medication in which countries mentioned?

Answer: Canada and the United States

Explanation: In both Canada and the United States, phytomenadione is classified as a prescription-only medication.

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What is the CAS Registry Number for phytomenadione?

Answer: 84-80-0

Explanation: The Chemical Abstracts Service (CAS) Registry Number uniquely identifying phytomenadione is 84-80-0.

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Which identifier is used for phytomenadione in the DrugBank database?

Answer: DB01022

Explanation: Phytomenadione is listed in the DrugBank database under the identifier DB01022.

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Which identifier is used for phytomenadione in the KEGG database?

Answer: D00148

Explanation: Phytomenadione is identified in the Kyoto Encyclopedia of Genes and Genomes (KEGG) database with the code D00148.

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