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Ingavirin

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ACTIVE PHARMA INGREDIENTS

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1 API Suppliers
1 USDMF

Synopsis

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Chemistry

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Also known as: 219694-63-0, Ingamine, Imidazolyl ethanamide pentandioic acid, Pentanedioic acid imidazolyl ethanamide, 4-{[2-(1h-imidazol-5-yl)ethyl]carbamoyl}butanoic acid, 3cm03muj69

Molecular Formula

C₁₀H₁₅N₃O₃

Molecular Weight

225.24 g/mol

InChI Key

KZIMLUFVKJLCCH-UHFFFAOYSA-N

FDA UNII

3CM03MUJ69

Imidazolyl Ethanamide Pentandioic Acid is an orally bioavailable small molecule, with potential hematopoiesis inducing and antiviral activities. Upon oral administration, myelo001 stimulates the differentiation of bone marrow cells of the leukocytic, lymphocytic, and erythrocytic lineages, and prevents apoptosis of hematopoietic cells. This prevents chemotherapy-induced neutropenia (CIN), inhibits the risk of infections, increases tolerance and allows for the continuation of the neutropenia-inducing chemotherapeutic agent. In addition, myelo 001 has antiviral properties.

1 2D Structure

Ingavirin

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

5-[2-(1H-imidazol-5-yl)ethylamino]-5-oxopentanoic acid

2.1.2 InChI

InChI=1S/C10H15N3O3/c14-9(2-1-3-10(15)16)12-5-4-8-6-11-7-13-8/h6-7H,1-5H2,(H,11,13)(H,12,14)(H,15,16)

2.1.3 InChI Key

KZIMLUFVKJLCCH-UHFFFAOYSA-N

2.1.4 Canonical SMILES

C1=C(NC=N1)CCNC(=O)CCCC(=O)O

2.2 Other Identifiers

2.2.1 UNII

3CM03MUJ69

2.3 Synonyms

2.3.1 MeSH Synonyms

1. 5-(2-(1h-imidazol-4-yl)ethylamino)-5-oxopentanoic Acid

2. Dicarbamin

3. Imidazolyl Ethanamide Pentandioic Acid

4. Pentanedioic Acid Imidazolyl Ethanamide

5. Vitaglutam

2.3.2 Depositor-Supplied Synonyms

1. 219694-63-0

2. Ingamine

3. Imidazolyl Ethanamide Pentandioic Acid

4. Pentanedioic Acid Imidazolyl Ethanamide

5. 4-{[2-(1h-imidazol-5-yl)ethyl]carbamoyl}butanoic Acid

6. 3cm03muj69

7. Pentanoic Acid, 5-[[2-(1h-imidazol-4-yl)ethyl]amino]-5-oxo-

8. 4-[2-(1h-imidazol-4-yl)-ethylcarbamoyl]-butyric Acid

9. Dicarbamin

10. Vitaglutam

11. Pentanoic Acid, 5-((2-(1h-imidazol-4-yl)ethyl)amino)-5-oxo-

12. Agn-pc-0mw29y

13. 4-([2-(1h-imidazol-5-yl)ethyl]carbamoyl)butanoic Acid

14. 5-[2-(1h-imidazol-5-yl)ethylamino]-5-oxopentanoic Acid

15. Unii-3cm03muj69

16. Schembl8282926

17. Chembl4297291

18. Schembl18381264

19. 5-(2-(1h-imidazol-4-yl)ethylamino)-5-oxopentanoic Acid

20. Dtxsid90433141

21. Zinc40493529

22. Akos002807987

23. Db11944

24. D11250

25. F75163

26. Imidazolyl Ethanamide Pentandioic Acid [who-dd]

27. Q27257036

28. 4-{[2-(1h-imidazol-5-yl)ethyl]carbamoyl}butanoicacid

29. 6-(2-(1h-imidazol-4-yl)ethylamino)-5-oxohexanoic Acid

30. 5-((2-(1h-imidazol-5-yl)ethyl)amino)-5-oxopentanoic Acid

2.4 Create Date

2006-10-25

3 Chemical and Physical Properties

Molecular Formula	C₁₀H₁₅N₃O₃
Molecular Weight	225.24 g/mol
XLogP3	-0.7
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	7
Exact Mass	225.11134135 g/mol
Monoisotopic Mass	225.11134135 g/mol
Topological Polar Surface Area	95.1 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	246
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	1

4 Pharmacology and Biochemistry

4.1 MeSH Pharmacological Classification

Antiviral Agents

Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly. (See all compounds classified as Antiviral Agents.)

4.2 ATC Code

J - Antiinfectives for systemic use

J05 - Antivirals for systemic use

J05A - Direct acting antivirals

J05AX - Other antivirals

J05AX21 - Pentanedioic acid imidazolyl ethanamide

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