드러그인포 약품요약정보

허가정보

항목

내용

청구코드(KD코드)
비급여점검코드
상한금액

650901060[E50310111] [보험코드에 따른 약품기본정보 직접조회]
\295 원/1정(2017.02.01)(현재약가)
\295 원/1정(2014.02.01)(변경전약가)
[상병코드조회]
[질병코드조회]

빠른조회


요약정보	[효능] [용법] [금기] [신중투여] [이상반응]

상세정보	[효능] [용법] [경고] [금기] [신중투여] [이상반응] [일반주의] [상호작용] [임산부] [수유부] [소아] [고령자] [신장애환자] [간장애환자] [적용주의] [과량투여] [임상검사치] [보관] [기타]

제품성상

긴 타원형의 광택이 있는 황색 필름코팅정 [제형정보 확인]

포장·유통단위

100정(20정/PTP포장×5)

포장·코드단위

약품규격	단위	포장형태	대표코드	표준코드	비고
105밀리그램	100 정	PTP	8806509010609	8806509010616

주성분코드

434700ATB [동일한 주성분코드를 가진 오리지날 또는 제네릭 의약품 조회]

허가사항 원문조회

[허가사항 원문조회]

효능효과

[적응증 별 검색]

성인 기준으로 1일 식이 단백 섭취량이 40g 이하로 제한되어 있는 만성 신부전환자에서 불완전한 단백질 대사로 인한 손상 감소

용법용량

* 절대 임의복용하지 마시고 반드시 의사 또는 약사와 상담하시기 바랍니다.

[처방약어]
통상적으로 70kg 성인을 기준으로 저단백식이(단백질 0.3-0.4g/kg/day)와 병용하여, 1회 4-8정씩, 1일 3회 식사 중에 씹지말고 그대로 복용한다.

[BMI지수 계산] [Body Surface Area 계산] [Cockcroft-Gault GFR 계산] [MDRD GFR 계산]

금기

가. 고 칼슘혈증 환자

나. 아미노산 대사 장애 환자

다. 이 약의 성분에 대해 과민반응을 보이는 경우

라. 페닐케톤뇨증 대사 장애가 있는 경우 (이 약에는 페닐알라닌이 함유되어 있음)

이상반응

1. 이상반응

가. 고칼슘혈증 : 고칼슘혈증이 나타날 수 있으므로 이런 경우에는 비타민 D의 섭취를 줄인다. 만약 고칼슘혈증이 지속된다면 이 약과 다른 칼슘원의 양을 줄인다.

나. 소화기장애 : 드물게 상복부 불쾌감이 나타날 수 있다.

2. 국내 시판 후 조사

국내에서 재심사를 위하여 6년 동안 638명의 환자를 대상으로 실시한 시판 후 조사 결과 이상반응의 발현 증례율은 인과관계와 상관없이 2.19%(14명/638명,19건)로 보고되었다. 이 중 약물과의 인과관계를 배제할 수 없는 이상반응 발현율은 1.25%(8명/638명, 13건)이며 다음과 같다. 소화불량, 오심이 각 0.47%(3명/638명)로 가장 많았으며, 변비, 복통이 각 0.31%(2명/638명),구토, 설사, 두통이 각 0.16%(1명/638명)로 나타났다. 예상하지 못한 약물 이상반응은 소화불량, 오심이 각 3건, 변비, 복통이 각 2건, 구토, 설사, 두통이 각 1건씩으로 보고되었다.

[주요 이상반응정보]

상호작용

가. 이 약과 다른 칼슘함유 제제를 병용했을 때 혈청 칼슘 농도가 증가되거나 강화될 수 있다.

나. 이 약을 투여하여 혈액 칼슘 농도가 올라가면 강심배당체의 작용을 증가시켜 심장 리듬 장애 위험을 증가시킬 수 있다.

다. 이 약 투여 중 혈청 인산 농도가 감소하므로 인산결합제(예, 수산화알루미늄)의 용량을 줄여야 한다.

라. 칼슘과 결합하는 약물들(예, 테트라사이클린, 시프로플록사신, 노르플록사신과 같은 항생제, 철분, 불소, 에스트라머스틴 함유 제제)의 흡수를 방해하지 않기 위해서, 이 약과의 병용 시 적어도 2시간 이상의 간격을 두어야 한다.

마. 이 약 이 외 다른 약물을 복용하고 있는 경우에는 담당 의사 및 약사에게 알려 상담한다.

Off-label Usage

[조회]

정보요약

드럭인포 의약품 요약/상세정보

코드 및 분류정보

항목	내용
주성분코드	434700ATB [동일한 주성분코드를 가진 오리지날 또는 제네릭 의약품 조회]
대표코드	8806509010609
BIT 약효분류	경장영양제(Enteral Nutritional Products)
ATC 코드	PROTEIN SUPPLEMENTS / V06B [코드분류상세설명] [ATC코드예측]
복지부분류코드	325 (단백아미노산제제 )
의약품 바코드정보	내용보기 케토스테릴정/E50310111 제품규격:/제품수량:100/제형:정 폼목기준코드:200210593 /대표코드:8806509010609/표준코드:8806509010616 구바코드:-/비고:백
주성분코드 분석 및 중복처방 검토	[주성분코드 분석 및 중복처방 검토]
Drugs By Indication	[전체보기]
Drugs By Classification	[전체보기]

제품정보

항목	내용
청구코드(KD코드) 비급여점검코드 상한금액	650901060[E50310111] [보험코드에 따른 약품기본정보 직접조회] \295 원/1정(2017.02.01)(최신약가) \295 원/1정(2014.02.01)(변경전약가) [상병코드조회] [질병코드집 다운로드]
제품성상	긴 타원형의 광택이 있는 황색 필름코팅정 [제형정보 확인]
대체관련	대조약
포장·유통단위	100정(20정/PTP포장×5)
보관방법	기밀용기, 25℃이하에서 보관
동일주성분코드 검색순위	유료정보입니다.

복약정보

항목	내용
LACTmed 바로가기	[바로가기]
약리작용	유료정보입니다.
축약복약지도	유료정보입니다.
복약지도	유료정보입니다.
병용금기 및 연령대금기 근거조회	[병용금기 및 연령대금기 근거조회]
보관상 주의
조제시 주의

심사정보

항목	내용
심사지침검색	[심평원 심사지침열람]
DUR 관련 고시	[병용연령금기 의약품 / 임부금기 의약품 / 비용효과적 함량 의약품 / 안전성 관련 급여중지 의약품]

학술정보

항목	내용
DUR (의약품사용평가)	병용금기 : 고시된 병용금기 내용은 없습니다. [상호작용/병용금기검색] 연령대금기 : 고시된 연령금기 내용은 없습니다. [연령대금기상세검색]
독성정보	Calcium에 대한 독성정보 : 정보보기 출처: 국립독성과학원 독성물질정보DB : http://www.nitr.go.kr/nitr/contents/m134200/view.do
Mechanism of Action	L-histidine에 대한 Mechanism_Of_Action 정보 Since the actions of supplemental L-histidine are unclear, any postulated mechanism is entirely speculative. However, some facts are known about L-histidine and some of its metabolites, such as histamine and trans-urocanic acid, which suggest that supplemental L-histidine may one day be shown to have immunomodulatory and/or antioxidant activities. Low free histidine has been found in the serum of some rheumatoid arthritis patients. Serum concentrations of other amino acids have been found to be normal in these patients. L-histidine is an excellent chelating agent for such metals as copper, iron and zinc. Copper and iron participate in a reaction (Fenton reaction) that generates potent reactive oxygen species that could be destructive to tissues, including joints. L-histidine is the obligate precursor of histamine, which is produced via the decarboxylation of the amino acid. In experimental animals, tissue histamine levels increase as the amount of dietary L-histidine increases. It is likely that this would be the case in humans as well. Histamine is known to possess immunomodulatory and antioxidant activity. Suppressor T cells have H2 receptors, and histamine activates them. Promotion of suppressor T cell activity could be beneficial in rheumatoid arthritis. Further, histamine has been shown to down-regulate the production of reactive oxygen species in phagocytic cells, such as monocytes, by binding to the H2 receptors on these cells. Decreased reactive oxygen species production by phagocytes could play antioxidant, anti-inflammatory and immunomodulatory roles in such diseases as rheumatoid arthritis. This latter mechanism is the rationale for the use of histamine itself in several clinical trials studying histamine for the treatment of certain types of cancer and viral diseases. In these trials, down-regulation by histamine of reactive oxygen species formation appears to inhibit the suppression of natural killer (NK) cells and cytotoxic T lymphocytes, allowing these cells to be more effective in attacking cancer cells and virally infected cells. L-lysine에 대한 Mechanism_Of_Action 정보 Proteins of the herpes simplex virus are rich in L-arginine, and tissue culture studies indicate an enhancing effect on viral replication when the amino acid ratio of L-arginine to L-lysine is high in the tissue culture media. When the ratio of L-lysine to L-arginine is high, viral replication and the cytopathogenicity of herpes simplex virus have been found to be inhibited. L-lysine may facilitate the absorption of calcium from the small intestine. L-threonine에 대한 Mechanism_Of_Action 정보 L-Threonine is a precursor to the amino acids glycine and serine. It acts as a lipotropic in controlling fat build-up in the liver. May help combat mental illness and may be very useful in indigestion and intestinal malfunctions. Also, threonine prevents excessive liver fat. Nutrients are more readily absorbed when threonine is present. L-tryptophan에 대한 Mechanism_Of_Action 정보 A number of important side reactions occur during the catabolism of tryptophan on the pathway to acetoacetate. The first enzyme of the catabolic pathway is an iron porphyrin oxygenase that opens the indole ring. The latter enzyme is highly inducible, its concentration rising almost 10-fold on a diet high in tryptophan. Kynurenine is the first key branch point intermediate in the pathway. Kynurenine undergoes deamniation in a standard transamination reaction yielding kynurenic acid. Kynurenic acid and metabolites have been shown to act as antiexcitotoxics and anticonvulsives. A second side branch reaction produces anthranilic acid plus alanine. Another equivalent of alanine is produced further along the main catabolic pathway, and it is the production of these alanine residues that allows tryptophan to be classified among the glucogenic and ketogenic amino acids. The second important branch point converts kynurenine into 2-amino-3-carboxymuconic semialdehyde, which has two fates. The main flow of carbon elements from this intermediate is to glutarate. An important side reaction in liver is a transamination and several rearrangements to produce limited amounts of nicotinic acid, which leads to production of a small amount of NAD⁺ and NADP⁺. L-tyrosine에 대한 Mechanism_Of_Action 정보 Tyrosine is produced in cells by hydroxylating the essential amino acid phenylalanine. This relationship is much like that between cysteine and methionine. Half of the phenylalanine required goes into the production of tyrosine; if the diet is rich in tyrosine itself, the requirements for phenylalanine are reduced by about 50%. The mechanism of L-tyrosine's antidepressant activity can be accounted for by the precursor role of L-tyrosine in the synthesis of the neurotransmitters norepinephrine and dopamine. Elevated brain norepinephrine and dopamine levels are thought to be associated with antidepressant effects. calcium에 대한 Mechanism_Of_Action 정보 Calcium plays a vital role in the anatomy, physiology and biochemistry of organisms and of the cell, particularly in signal transduction pathways. More than 500 human proteins are known to bind or transport calcium. The skeleton acts as a major mineral storage site for the element and releases Ca2+ ions into the bloodstream under controlled conditions. Circulating calcium is either in the free, ionized form or bound to blood proteins such as serum albumin. Parathyroid hormone (secreted from the parathyroid gland) regulates the resorption of Ca2+ from bone. Calcitonin stimulates incorporation of calcium in bone, although this process is largely independent of calcitonin. Although calcium flow to and from the bone is neutral, about 5 mmol is turned over a day. Bone serves as an important storage point for calcium, as it contains 99% of the total body calcium. Low calcium intake may also be a risk factor in the development of osteoporosis. The best-absorbed form of calcium from a pill is a calcium salt like carbonate or phosphate. Calcium gluconate and calcium lactate are absorbed well by pregnant women. Seniors absorb calcium lactate, gluconate and citrate better unless they take their calcium supplement with a full breakfast. The currently recommended calcium intake is 1,500 milligrams per day for women not taking estrogen and 800 milligrams per day for women on estrogen. There is close to 300 milligrams of calcium in one cup of fluid milk. Calcium carbonate is currently the best and least expensive form of calcium supplement available.
Pharmacology	L-histidine에 대한 Pharmacology 정보 Is found abundantly in hemoglobin; has been used in the treatment of rheumatoid arthritis, allergic diseases, ulcers and anemia. A deficiency can cause poor hearing. L-lysine에 대한 Pharmacology 정보 Insures the adequate absorption of calcium; helps form collagen ( which makes up bone cartilage & connective tissues); aids in the production of antibodies, hormones & enzymes. Recent studies have shown that Lysine may be effective against herpes by improving the balance of nutrients that reduce viral growth. A deficiency may result in tiredness, inability to concentrate, irritability, bloodshot eyes, retarded growth, hair loss, anemia & reproductive problems. L-threonine에 대한 Pharmacology 정보 L-Threonine is an essential amino acid that helps to maintain the proper protein balance in the body. It is important for the formation of collagen, elastin, and tooth enamel, and aids liver and lipotropic function when combined with aspartic acid and methionine. L-tryptophan에 대한 Pharmacology 정보 Tryptophan is critical for the production of the body's proteins, enzymes and muscle tissue. It is also essential for the production of niacin, the synthesis of the neurotransmitter serotonin and melatonin. Tryptophan supplements can be used as natural relaxants to help relieve insomnia. Tryptophan can also reduce anxiety and depression and has been shown to reduce the intensity of migraine headaches. Other promising indications include the relief of chronic pain, reduction of impulsivity or mania and the treatment of obsessive or compulsive disorders. Tryptophan also appears to help the immune system and can reduce the risk of cardiac spasms. Tryptophan deficiencies may lead to coronary artery spasms. Tryptophan is used as an essential nutrient in infant formulas and intravenous feeding. Tryptophan is marketed as a prescription drug (Tryptan) for those who do not seem to respond well to conventional antidepressants. It may also be used to treat those afflicted with seasonal affective disorder (a winter-onset depression). Tryptopan serves as the precursor for the synthesis of serotonin (5-hydroxytryptamine, 5-HT) and melatonin (N-acetyl-5-methoxytryptamine). L-tyrosine에 대한 Pharmacology 정보 Tyrosine is a nonessential amino acid synthesized in the body from phenylalanine. Tyrosine is critical for the production of the body's proteins, enzymes and muscle tissue. Tyrosine is a precursor to the neurotransmitters norepinephrine and dopamine. It can act as a mood elevator and an anti-depressant. It may improve memory and increase mental alertness. Tyrosine aids in the production of melanin and plays a critical role in the production of thyroxin (thyroid hormones). Tyrosine deficiencies are manifested by hypothyroidism, low blood pressure and low body temperature. Supplemental tyrosine has been used to reduce stress and combat narcolepsy and chronic fatigue.
Absorption	L-histidine에 대한 Absorption 정보 Absorbed from the small intestine via an active transport mechanism requiring the presence of sodium. L-lysine에 대한 Absorption 정보 Absorbed from the lumen of the small intestine into the enterocytes by an active transport process L-tyrosine에 대한 Absorption 정보 L-tyrosine is absorbed from the small intestine by a sodium-dependent active transport process.
Toxicity	L-histidine에 대한 Toxicity 정보 ORL-RAT LD₅₀ > 15000 mg/kg, IPR-RAT LD₅₀ > 8000 mg/kg, ORL-MUS LD₅₀ > 15000 mg/kg, IVN-MUS LD₅₀ > 2000 mg/kg; Mild gastrointestinal side effects. L-lysine에 대한 Toxicity 정보 Not Available L-tryptophan에 대한 Toxicity 정보 Oral rat LD₅₀: > 16 gm/kg. Investigated as a tumorigen, mutagen, reproductive effector. Symptoms of overdose include agitation, confusion, diarrhea, fever, overactive reflexes, poor coordination, restlessness, shivering, sweating, talking or acting with excitement you cannot control, trembling or shaking, twitching, and vomiting. L-tyrosine에 대한 Toxicity 정보 L-Tyrosine has very low toxicity. There have been very few reports of toxicity. LD₅₀ (oral, rat) > 5110 mg/kg.
Drug Interactions	L-histidine에 대한 Drug_Interactions 정보 Not Available L-lysine에 대한 Drug_Interactions 정보 Not Available L-tryptophan에 대한 Drug_Interactions 정보 Not Available L-tyrosine에 대한 Drug_Interactions 정보 Not Available calcium에 대한 Drug_Interactions 정보 Alendronate Formation of non-absorbable complexesAmprenavir The antiacid decreases the absorption of amprenavirAtazanavir This gastric pH modifier decreases the levels/effects of atazanavirChloroquine The antiacid decreases the absorption of chloroquineCiprofloxacin Formation of non-absorbable complexesDapsone Formation of non-absorbable complexesDelavirdine The antiacid decreases the effect of delavirdineDemeclocycline Formation of non-absorbable complexesDoxycycline Formation of non-absorbable complexesEnoxacin Formation of non-absorbable complexesFosamprenavir The antiacid decreases the absorption of amprenavirGrepafloxacin Formation of non-absorbable complexesIbandronate Formation of non-absorbable complexesIndinavir The antiacid decreases the absorption of indinavirItraconazole The antacid decreases the effect of the imidazoleKetoconazole The antacid decreases the effect of the imidazoleLevofloxacin Formation of non-absorbable complexesLevothyroxine Calcium decreases absorption of levothyroxineLomefloxacin Formation of non-absorbable complexesMethacycline Formation of non-absorbable complexesMinocycline Formation of non-absorbable complexesMoxifloxacin Formation of non-absorbable complexesNorfloxacin Formation of non-absorbable complexesOfloxacin Formation of non-absorbable complexesOxytetracycline Formation of non-absorbable complexesPefloxacin Formation of non-absorbable complexesPolystyrene sulfonate Formation of non-absorbable complexesRisedronate Formation of non-absorbable complexesTetracycline Formation of non-absorbable complexesTrovafloxacin Formation of non-absorbable complexesClodronate Formation of non-absorbable complexesEtidronic acid Formation of non-absorbable complexesMycophenolate mofetil Formation of non-absorbable complexesTemafloxacin Formation of non-absorbable complexes
CYP450 Drug Interaction	[CYP450 Table직접조회]
Drug Target	[Drug Target]
Description	L-histidine에 대한 Description 정보 An essential amino acid that is required for the production of histamine. [PubChem] L-lysine에 대한 Description 정보 L-Lysine (abbreviated as Lys or K)[1] is an 慣-amino acid with the chemical formula HO2CCH(NH2)(CH2)4NH2. This amino acid is an essential amino acid, which means that humans cannot synthesize it. Its codons are AAA and AAG.L-Lysine is a base, as are arginine and histidine. The 琯-amino group often participates in hydrogen bonding and as a general base in catalysis. Common posttranslational modifications include methylation of the 琯-amino group, giving methyl-, dimethyl-, and trimethyllysine. The latter occurs in calmodulin. Other posttranslational modifications include acetylation. Collagen contains hydroxylysine which is derived from lysine by lysyl hydroxylase. O-Glycosylation of lysine residues in the endoplasmic reticulum or Golgi apparatus is used to mark certain proteins for secretion from the cell. L-threonine에 대한 Description 정보 An essential amino acid occurring naturally in the L-form, which is the active form. It is found in eggs, milk, gelatin, and other proteins. [PubChem] L-tryptophan에 대한 Description 정보 An essential amino acid that is necessary for normal growth in infants and for nitrogen balance in adults. It is a precursor of indole alkaloids in plants. It is a precursor of serotonin (hence its use as an antidepressant and sleep aid). It can be a precursor to niacin, albeit inefficiently, in mammals. [PubChem] L-tyrosine에 대한 Description 정보 A non-essential amino acid. In animals it is synthesized from phenylalanine. It is also the precursor of epinephrine; thyroid hormones; and melanin. [PubChem] calcium에 대한 Description 정보 Calcium plays a vital role in the anatomy, physiology and biochemistry of organisms and of the cell, particularly in signal transduction pathways. The skeleton acts as a major mineral storage site for the element and releases Ca2+ ions into the bloodstream under controlled conditions. Circulating calcium is either in the free, ionized form or bound to blood proteins such as serum albumin. Although calcium flow to and from the bone is neutral, about 5 mmol is turned over a day. Bone serves as an important storage point for calcium, as it contains 99% of the total body calcium. Low calcium intake may also be a risk factor in the development of osteoporosis. The best-absorbed form of calcium from a pill is a calcium salt like carbonate or phosphate. Calcium gluconate and calcium lactate are absorbed well by pregnant women. Seniors absorb calcium lactate, gluconate and citrate better unless they take their calcium supplement with a full breakfast.
Dosage Form	L-histidine에 대한 Dosage_Form 정보 Capsule OralPowder OralTablet Oral L-lysine에 대한 Dosage_Form 정보 Not Available L-tryptophan에 대한 Dosage_Form 정보 Capsule OralTablet Oral L-tyrosine에 대한 Dosage_Form 정보 Not Available calcium에 대한 Dosage_Form 정보 Capsule OralLiquid DentalLiquid IntravenousLiquid OralLiquid SublingualPaste DentalPowder OralPowder, for solution OralSolution IntramuscularSolution IntravenousSolution OralSolution / drops OralSyrup OralTablet OralTablet, chewable Oral
Drug Category	L-histidine에 대한 Drug_Category 정보 Conditionally Essential Amino AcidsDietary supplementMicronutrient L-lysine에 대한 Drug_Category 정보 Dietary supplementEssential Amino AcidsMicronutrient L-threonine에 대한 Drug_Category 정보 Dietary supplementEssential Amino AcidsMicronutrient L-tryptophan에 대한 Drug_Category 정보 Antidepressive Agents, Second-GenerationDietary supplementEssential Amino AcidsMicronutrient L-tyrosine에 대한 Drug_Category 정보 Dietary supplementMicronutrientNon-Essential Amino Acids
Smiles String Canonical	L-histidine에 대한 Smiles_String_canonical 정보 NC(CC1=CN=CN1)C(O)=O L-lysine에 대한 Smiles_String_canonical 정보 NCCCCC(N)C(O)=O L-threonine에 대한 Smiles_String_canonical 정보 CC(O)C(N)C(O)=O L-tryptophan에 대한 Smiles_String_canonical 정보 NC(CC1=CNC2=CC=CC=C12)C(O)=O L-tyrosine에 대한 Smiles_String_canonical 정보 NC(CC1=CC=C(O)C=C1)C(O)=O calcium에 대한 Smiles_String_canonical 정보 Not Available calcium에 대한 Smiles_String_canonical 정보 Not Available calcium에 대한 Smiles_String_canonical 정보 Not Available calcium에 대한 Smiles_String_canonical 정보 Not Available
Smiles String Isomeric	L-histidine에 대한 Smiles_String_isomeric 정보 N[C@@H](CC1=CN=CN1)C(O)=O L-lysine에 대한 Smiles_String_isomeric 정보 NCCCC[C@H](N)C(O)=O L-threonine에 대한 Smiles_String_isomeric 정보 C[C@@H](O)[C@H](N)C(O)=O L-tryptophan에 대한 Smiles_String_isomeric 정보 N[C@@H](CC1=CNC2=CC=CC=C12)C(O)=O L-tyrosine에 대한 Smiles_String_isomeric 정보 N[C@@H](CC1=CC=C(O)C=C1)C(O)=O calcium에 대한 Smiles_String_isomeric 정보 Not Available
InChI Identifier	L-histidine에 대한 InChI_Identifier 정보 InChI=1/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m0/s1/f/h9-10H L-lysine에 대한 InChI_Identifier 정보 InChI=1/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)/t5-/m0/s1/f/h9H L-threonine에 대한 InChI_Identifier 정보 InChI=1/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3+/m1/s1/f/h7H L-tryptophan에 대한 InChI_Identifier 정보 InChI=1/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m0/s1/f/h14H L-tyrosine에 대한 InChI_Identifier 정보 InChI=1/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m0/s1/f/h12H calcium에 대한 InChI_Identifier 정보 Not Available
Chemical IUPAC Name	L-histidine에 대한 Chemical_IUPAC_Name 정보 (2S)-2-amino-3-(3H-imidazol-4-yl)propanoic acid L-lysine에 대한 Chemical_IUPAC_Name 정보 (2S)-2,6-diaminohexanoic acid L-threonine에 대한 Chemical_IUPAC_Name 정보 (2S,3R)-2-amino-3-hydroxybutanoic acid L-tryptophan에 대한 Chemical_IUPAC_Name 정보 (2S)-2-amino-3-(1H-indol-3-yl)propanoic acid L-tyrosine에 대한 Chemical_IUPAC_Name 정보 (2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid calcium에 대한 Chemical_IUPAC_Name 정보 Not Available
Drug-Induced Toxicity Related Proteins	LYSINE 의 Drug-Induced Toxicity Related Protein정보 Replated Protein:Tamm-Horsfall protein Drug:Lysine Toxicity:persisting acute renal failure . [바로가기] METHIONINE 의 Drug-Induced Toxicity Related Protein정보 Replated Protein:NMDA receptor-regulated protein Drug:methionine Toxicity:cerebrovascular disease. [바로가기] Replated Protein:Cystathionine beta-synthase Drug:methionine Toxicity:lipoprotein peroxidation and platelet aggregation. [바로가기] Replated Protein:Methylenetetrahydrofolate reductase Drug:methionine Toxicity:lipoprotein peroxidation and platelet aggregation. [바로가기]

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