Weight | 134.087 g/mol |
---|---|
Formula | C4H6O5 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
malic acid
malate · malic acid, disodium salt, (S)-isomer · calcium (hydroxy-1-malate) hexahydrate
78644-42-5, 6915-15-7, 617-48-1
Score:
#1117 in Biology
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#1261 in Chemistry
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- Sigma-Aldrich - malic acid24.10 - 374.85 USD
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- Sunitinib Malate for the Treatment of Pancreatic Neuroendocrine Tumors (The New England Journal of Medicine, 2011)
- Aluminum Tolerance in Wheat (Triticum aestivum L.) (II. Aluminum-Stimulated Excretion of Malic Acid from Root Apices). (Plant Physiology, 1993)
- A wheat gene encoding an aluminum activated malate transporter (Plant Journal, 2004)
- Phase II Study of Sunitinib Malate, an Oral Multitargeted Tyrosine Kinase Inhibitor, in Patients With Metastatic Breast Cancer Previously Treated With an Anthracycline and a Taxane (Journal of Clinical Oncology, 2008)
- Root-Secreted Malic Acid Recruits Beneficial Soil Bacteria (Plant Physiology, 2008)
- Multiple circulating proangiogenic factors induced by sunitinib malate are tumor-independent and correlate with antitumor efficacy (Proceedings of the National Academy of Sciences of the United States of America, 2007)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - malate
- malic acid, disodium salt, (S)-isomer
- calcium (hydroxy-1-malate) hexahydrate
- malic acid, magnesium salt (2:1)
- malic acid, disodium salt, (R)-isomer
- malic acid, (R)-isomer
- malic acid, potassium salt, (R)-isomer
- malic acid, calcium salt, (1:1), (S)-isomer
- malic acid, disodium salt
- malic acid, monopotassium salt, (+-)-isomer
- malic acid, sodium salt, (+-)-isomer
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SMILESC(C(C(=O)O)O)C(=O)O
-
InChIKeyBJEPYKJPYRNKOW-UHFFFAOYSA-N
- Pubchem - malic acid
- Wikipedia - malic acid
Malic acid is an organic compound with the molecular formula C4H6O5. It is a dicarboxylic acid that is made by all living organisms, contributes to the pleasantly sour taste of fruits, and is used as a food additive. Malic acid has two stereoisomeric forms (L- and D-enantiomers), though only the L-isomer exists naturally.
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