Find Zinc Picolinate manufacturers, exporters & distributors on PharmaCompass

Zinc Picolinate

Zinc Picolinate

Synopsis, Chemistry

APIs // Active Pharmaceutical Ingredients

3 API Suppliers, 3 Listed Suppliers

PRICE INFORMATION

API Reference Price, API Exports

MARKET PLACE

4 APIs

4 APIs

Product Search

API SUPPLIERS

API Suppliers

US DMFs Filed

CEP/COS Certifications

JDMFs Filed

Other Certificates

Other Suppliers

API REF. PRICE (USD / KG)

API Market Place

INTERMEDIATES

DOSSIERS // FDF

USA (Orange Book)

Europe

Canada

Australia

South Africa

Uploaded Dossiers

GLOBAL SALES (USD Million)

U.S. Medicaid

Annual Reports

FDF Market Place

EXCIPIENTS

PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

USFDA Exclusivities

DIGITAL CONTENT

Blog #PharmaFlow

News

REF STANDARD

EDQM

USP

Other Listed Suppliers

SERVICES

Also known as: 17949-65-4, Zincpicolinate, Zinc;pyridine-2-carboxylate, Alo92o31se, Picolinic acid zinc salt, Unii-alo92o31se

Molecular Formula

C₁₂H₈N₂O₄Zn

Molecular Weight

309.6 g/mol

InChI Key

NHVUUBRKFZWXRN-UHFFFAOYSA-L

FDA UNII

ALO92O31SE

Zinc Picolinate is a dietary zinc supplement containing the zinc salt of picolinic acid, that can be used to prevent or treat zinc deficiency, and with immunomodulatory activity. Upon administration, zinc picolinate supplements zinc. As an essential trace element, zinc is of key importance in many biological processes. It plays an important role in the proper functioning of the both the innate and adaptive immune system. Zinc inhibits the production of pro-inflammatory mediators and prevents inflammation. It acts as an antioxidant, prevents oxidative damage and protects cells against DNA damage. Zinc is required for the enzyme activities necessary for cell division, cell growth, and wound healing.

1 2D Structure

Zinc Picolinate

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

zinc;pyridine-2-carboxylate

2.1.2 InChI

InChI=1S/2C6H5NO2.Zn/c2*8-6(9)5-3-1-2-4-7-5;/h2*1-4H,(H,8,9);/q;;+2/p-2

2.1.3 InChI Key

NHVUUBRKFZWXRN-UHFFFAOYSA-L

2.1.4 Canonical SMILES

C1=CC=NC(=C1)C(=O)[O-].C1=CC=NC(=C1)C(=O)[O-].[Zn+2]

2.2 Other Identifiers

2.2.1 UNII

ALO92O31SE

2.3 Synonyms

2.3.1 MeSH Synonyms

1. 2-pyridine Carboxylic Acid

2. 2-pyridinecarboxylic Acid

3. Calcium Dipicolinate Trihydrate

4. Chromium Picolinate

5. Iron(iii) Picolinate

6. Picolinate

7. Picolinic Acid

8. Picolinic Acid, Hydrochloride

9. Picolinic Acid, Sodium Salt

10. Pyridine-2-carboxylic Acid

2.3.2 Depositor-Supplied Synonyms

1. 17949-65-4

2. Zincpicolinate

3. Zinc;pyridine-2-carboxylate

4. Alo92o31se

5. Picolinic Acid Zinc Salt

6. Unii-alo92o31se

7. Zinc Pyridine-2-carboxylate

8. Dipicolinic Acid Zinc Salt

9. Schembl177833

10. Zinc Picolinate [inci]

11. Dtxsid60170814

12. Zinc Picolinate [who-dd]

13. Mfcd00145544

14. Akos015918238

15. Db11175

16. Ft-0652546

17. 2-pyridinecarboxylic Acid, Zinc Complex

18. A812451

19. J-011457

20. Q27273986

2.4 Create Date

2006-10-25

3 Chemical and Physical Properties

Molecular Formula	C₁₂H₈N₂O₄Zn
Molecular Weight	309.6 g/mol
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	0
Exact Mass	307.977549 g/mol
Monoisotopic Mass	307.977549 g/mol
Topological Polar Surface Area	106 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	108
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	3

4 Pharmacology and Biochemistry

4.1 MeSH Pharmacological Classification

Iron Chelating Agents

Organic chemicals that form two or more coordination links with an iron ion. Once coordination has occurred, the complex formed is called a chelate. The iron-binding porphyrin group of hemoglobin is an example of a metal chelate found in biological systems. (See all compounds classified as Iron Chelating Agents.)