Orotic acid - 10mM in DMSO, high purity , CAS No.65-86-1

Item Number
O425324
Grouped product items
SKUSizeAvailabilityPrice Qty
O425324-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$69.90

Intermediate in pyrimidine metabolism

Basic Description

SynonymsOrotic acid | 65-86-1 | 6-Carboxyuracil | Oropur | Orodin | Orotonin | Orotyl | Orotonsan | Vitamin B13 | Whey factor | Oroturic | 2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid | Uracil-6-carboxylic acid | Animal galactose factor | 6-Uracilcarboxylic acid | Molkensaeure | Oro
Specifications & PurityMoligand™, 10mM in DMSO
Biochemical and Physiological MechanismsIntermediate in pyrimidine metabolism. Increases hepatic triacylglycerol levels in vivo . Cardioprotective.
Storage TempStore at -80°C
Shipped InIce chest + Ice pads
GradeMoligand™
Product Description

Orotic acid is a heterocyclic compound and an acid. It was once believed to be part of the vitamin B complex and was called vitamin B13, but it is now known that it is not a vitamin but is instead manufactured in the body by intestinal flora. Its salts, known as orotates, are sometimes used as mineral carriers in some dietary supplements, to increase their bioavailability. It is an intermediate in de novo pyrimidine biosynthesis that may be used to study the specificity and kinetics of orotate phosphoribosyltransferase (OPRT) which catalyzes the reversible phosphoribosyl transfer from 5′-phospho-α-d-ribose 1′-diphosphate (PRPP) to orotic acid, forming pyrophosphate and orotidine 5′-monophosphate (OMP). It may be used to study dependent cell signaling pathways and transcription regulation mechanisms that induce hepatic lipogenesis.
An intermediate in de novo pyrimidine biosynthesis.

Associated Targets(Human)

DHODH Tclin Dihydroorotate dehydrogenase (quinone), mitochondrial (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SLC2A9 Tbio Solute carrier family 2, facilitated glucose transporter member 9 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
HDAC6 Tclin Histone deacetylase 6 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
LMNA Tbio Prelamin-A/C (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALDH1A1 Tchem Retinal dehydrogenase 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC2A9 Tbio Solute carrier family 2, facilitated glucose transporter member 9 (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DHODH Dihydroorotate dehydrogenase (fumarate) (195 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 2,4-dioxo-1H-pyrimidine-6-carboxylic acid
INCHI InChI=1S/C5H4N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h1H,(H,9,10)(H2,6,7,8,11)
InChi Key PXQPEWDEAKTCGB-UHFFFAOYSA-N
Canonical SMILES C1=C(NC(=O)NC1=O)C(=O)O
Isomeric SMILES C1=C(NC(=O)NC1=O)C(=O)O
WGK Germany 3
RTECS RM3180000
PubChem CID 967
Molecular Weight 156.1
Beilstein 383901

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

WGK Germany 3
RTECS RM3180000

Related Documents

Citations of This Product

1. Yongyan Yang, Gangying Feng, Jingfei Wang, Ruiting Zhang, Shuangling Zhong, Jia Wang, Xuejun Cui.  (2023)  Injectable chitosan-based self-healing supramolecular hydrogels with temperature and pH dual-responsivenesses.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  227  (1038).  [PMID:36460241] [10.1016/j.ijbiomac.2022.11.279]
2. Feng Ye, Qiufeng Ye, Haihua Zhan, Yeqian Ge, Xiaotao Ma, Yingying Xu, Xu Wang.  (2019)  Synthesis and Study of Zinc Orotate and Its Synergistic Effect with Commercial Stabilizers for Stabilizing Poly(Vinyl Chloride).  Polymers,  11  (2): (194).  [PMID:30960179] [10.3390/polym11020194]
3. Yongqi Feng, Piming Ma, Pengwu Xu, Ruyin Wang, Weifu Dong, Mingqing Chen, Cornelis Joziasse.  (2018)  The crystallization behavior of poly(lactic acid) with different types of nucleating agents.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  106  (955).  [PMID:28830776] [10.1016/j.ijbiomac.2017.08.095]
4. Wei Yin, Huihui Chai, Renhua Liu, Changhu Chu, John A. Palasota, Xiaohui Cai.  (2015)  Click N-benzyl iminodiacetic acid: Novel silica-based tridentate zwitterionic stationary phase for hydrophilic interaction liquid chromatography.  TALANTA,  132  (137).  [PMID:25476290] [10.1016/j.talanta.2014.08.077]
5. Hongyue Guo, Renhua Liu, Jinjin Yang, Bingcheng Yang, Xinmiao Liang, Changhu Chu.  (2012)  A novel click lysine zwitterionic stationary phase for hydrophilic interaction liquid chromatography.  JOURNAL OF CHROMATOGRAPHY A,  1223  (47).  [PMID:22226552] [10.1016/j.chroma.2011.12.033]

References

1. Yongyan Yang, Gangying Feng, Jingfei Wang, Ruiting Zhang, Shuangling Zhong, Jia Wang, Xuejun Cui.  (2023)  Injectable chitosan-based self-healing supramolecular hydrogels with temperature and pH dual-responsivenesses.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  227  (1038).  [PMID:36460241] [10.1016/j.ijbiomac.2022.11.279]
2. Feng Ye, Qiufeng Ye, Haihua Zhan, Yeqian Ge, Xiaotao Ma, Yingying Xu, Xu Wang.  (2019)  Synthesis and Study of Zinc Orotate and Its Synergistic Effect with Commercial Stabilizers for Stabilizing Poly(Vinyl Chloride).  Polymers,  11  (2): (194).  [PMID:30960179] [10.3390/polym11020194]
3. Yongqi Feng, Piming Ma, Pengwu Xu, Ruyin Wang, Weifu Dong, Mingqing Chen, Cornelis Joziasse.  (2018)  The crystallization behavior of poly(lactic acid) with different types of nucleating agents.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  106  (955).  [PMID:28830776] [10.1016/j.ijbiomac.2017.08.095]
4. Wei Yin, Huihui Chai, Renhua Liu, Changhu Chu, John A. Palasota, Xiaohui Cai.  (2015)  Click N-benzyl iminodiacetic acid: Novel silica-based tridentate zwitterionic stationary phase for hydrophilic interaction liquid chromatography.  TALANTA,  132  (137).  [PMID:25476290] [10.1016/j.talanta.2014.08.077]
5. Hongyue Guo, Renhua Liu, Jinjin Yang, Bingcheng Yang, Xinmiao Liang, Changhu Chu.  (2012)  A novel click lysine zwitterionic stationary phase for hydrophilic interaction liquid chromatography.  JOURNAL OF CHROMATOGRAPHY A,  1223  (47).  [PMID:22226552] [10.1016/j.chroma.2011.12.033]

Solution Calculators