L-proline CHEBI 17203

Proline

L-Proline is an osmoprotectant and therefore is used in many pharmaceutical biotechnological applications The growth medium used in plant tissue culture may be supplemented with proline This can increase growth perhaps because it helps the plant tolerate the stresses of tissue culture [better source needed] For proline's role in the stress response of plants see Biological activity

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L(

l-proline proline l---proline s-pyrrolidine-2-carboxylic acid 2-pyrrolidinecarboxylic acid --proline --s-proline 2s-pyrrolidine-2-carboxylic acid prolinum h-pro-oh: InChI Key: ONIBWKKTOPOVIA-BYPYZUCNSA-N: IUPAC Name (2S)-pyrrolidine-2-carboxylic acid: PubChem CID: 145742: Formula Weight: 115 13: Physical Form: Crystals or Crystalline

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L

CHEBI:17203: ChEBI ASCII Name L-proline: Definition Pyrrolidine in which the pro-S hydrogen at position 2 is substituted by a carboxylic acid group L-Proline is the only one of the twenty DNA-encoded amino acids which has a secondary amino group α to the carboxyl group It is an essential component of collagen and is important for proper

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Urea cycle and metabolism of amino groups (Rattus

Fumarate CO2 Ala and aspartate metabolism Spermidine L-Glutamate-5-semialdehyde C03406 Guanidinoacetate L-Aspartate N-Methylhydantoin N-Acetyl-L-glutamate (S)-1-Pyrroline-5-carboxylate Sarcosine L-Glutamate creatine-P Creatinine L-Proline Pyrimidine metabolism Creatine Arginine Glutamate metabolism Phosphoguanidinoacetate L-Ornithine Carbamoyl-P N-Carbamoylsarcosine

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L-Proline is the only one of the twenty DNA-encoded amino acids which has a secondary amino group alpha to the carboxyl group It is an essential component of collagen and is important for proper functioning of joints and tendons It also helps maintain and strengthen heart muscles

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proline (CHEBI:26271)

1-propanoylproline (CHEBI:86343) has functional parent proline (CHEBI:26271) proline derivative (CHEBI:26273) has functional parent proline (CHEBI:26271) D-proline (CHEBI:16313) is a proline (CHEBI:26271) L-proline (CHEBI:17203) is a proline (CHEBI:26271) prolinium (CHEBI:32872) is conjugate acid of proline (CHEBI:26271) prolinate (CHEBI:32871) is conjugate base of proline

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Vitamin B6

1 TNSALP Pyridoxine dependent epilepsy (PDE) Diet Lysine degradation pathway Fig 11 2 PNPO 2-keto 6-aminocaproic acid L-lysine ALPL IP P5C dehydrogenase pyridoxal Pipecolic acid P5C PLP pyridoxamine-p Pyridoxal-P Antiquitin PLP piperideine-2-carboxylate Vitamin B6 pyridoxal glutamic semialdehyde Saccharopine PIGV anchor pyridoxamine-p L-proline Pyridoxine-P pyridoxamine

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1 Body Joint Support Reviews: Does It Work?

L-Proline – It is an amino acid that plays a key role in fortifying connective tissues surrounding the joints [2] ApresFlex – It is made from Boswellia extract and said to delay the deterioration of essential collagen in the body Turmeric – It has natural anti-inflammatory properties and it is also made up of powerful antioxidants that work to shield joints from damage caused by

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L

L-Proline Multi-Compendial U S P J T Baker™ 1kg Poly Bottle Amino Acids Biochemicals English English Change Country Sign-up for Email Customer Service - 01509 555 500 English English Change Country 0 No offer available Chemical Structure Product Certificates Safety Data Sheets Order Status New Offers Order By Product Code Shop Products Antibodies Protein Biology

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Trans

trans-4-hydroxy-l-proline hydroxyproline l-hydroxyproline 2s 4r-4-hydroxypyrrolidine-2-carboxylic acid 4-hydroxy-l-proline l-4-hydroxyproline hydroxy-l-proline trans-4-hydroxyproline h-hyp-oh hypro: ChEBI: CHEBI:18095: SMILES: C1C(CNC1C(=O)O)O: Summenformel: C 5 H 9 NO 3: InChI-Schlssel: PMMYEEVYMWASQN-DMTCNVIQSA-N: PubChem-CID : 5810: IUPAC-Name (2S 4R)-4

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1 Body Joint Support Reviews: Does It Work?

L-Proline – It is an amino acid that plays a key role in fortifying connective tissues surrounding the joints [2] ApresFlex – It is made from Boswellia extract and said to delay the deterioration of essential collagen in the body Turmeric – It has natural anti-inflammatory properties and it is also made up of powerful antioxidants that work to shield joints from damage caused by

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CharChem Органическое вещество Органические

Поиск химических веществ по названиям или формулам Справочник содержит названия веществ и описания химических формул (в т ч структурные формулы и скелетные формулы)

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L

185 C (Decomposes Literature) Indofine [04-1529] 185 C (Decomposes) Alfa Aesar 185 C (Decomposes) OU Chemical Safety Data (No longer updated) More details 185 C Jean-Claude Bradley Open Melting Point Dataset 16650: 185 C (Decomposes) Alfa Aesar A14201 215 C Biosynth Q-100459: 185 C (Decomposes Literature) Indofine [04-1529] [04-1529]

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KEGG COMPOUND: C00037

Undecylprodigiosin biosynthesis L-proline = undecylprodigiosin: Enzyme: 1 5 1 1 1 5 1 2 1 5 1 21 1 5 1 49 1 5 5 2 ChEBI: 17203: ChEMBL: CHEMBL54922: KNApSAcK: C00001388: PDB-CCD: PRO : 3DMET: B01173: NIKKAJI: J9 117K: LinkDB: KCF data: ATOM 8 1 C1x C 10 0100 -19 3900 2 C1x C 10 4300 -20 6500 3 C1x C 11 8300 -20 6500 4 C1y C 12 2500 -19 3200 5 N1x N 11 1300 -18 4800 6

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trans

trans-4-Hydroxy-L-proline ≥99% Synonym: (2S 4R)-4-Hydroxypyrrolidine-2-carboxylic acid Hyp CAS Number 51-35-4 Empirical Formula (Hill Notation) C 5 H 9 NO 3 Molecular Weight 131 13 Beilstein/REAXYS Number 81441 EC Number 200-091-9 MDL number MFCD00064320 PubChem Substance ID 24895692 NACRES NA 22

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L-Proline is the only one of the twenty DNA-encoded amino acids which has a secondary amino group alpha to the carboxyl group It is an essential component of collagen and is important for proper functioning of joints and tendons It also helps maintain and strengthen heart muscles

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CharChem Аминокислоты

Поиск химических веществ по названиям или формулам Справочник содержит названия веществ и описания химических формул (в т ч структурные формулы и скелетные формулы)

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