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2D Structure
Also known as: 80714-61-0, Acth (4-7), pro-gly-pro-, Mehfpgp, Met-glu-his-phe-pro-gly-pro, I5fal2585h, Acth (4-7), prolyl-glycyl-proline-
Molecular Formula
C37H51N9O10S
Molecular Weight
813.9  g/mol
InChI Key
AFEHBIGDWIGTEH-AQRCPPRCSA-N
FDA UNII
I5FAL2585H

1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
(2S)-1-[2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-4-methylsulfanylbutanoyl]amino]-4-carboxybutanoyl]amino]-3-(1H-imidazol-5-yl)propanoyl]amino]-3-phenylpropanoyl]pyrrolidine-2-carbonyl]amino]acetyl]pyrrolidine-2-carboxylic acid
2.1.2 InChI
InChI=1S/C37H51N9O10S/c1-57-16-13-24(38)32(50)42-25(11-12-31(48)49)33(51)43-26(18-23-19-39-21-41-23)34(52)44-27(17-22-7-3-2-4-8-22)36(54)46-15-5-9-28(46)35(53)40-20-30(47)45-14-6-10-29(45)37(55)56/h2-4,7-8,19,21,24-29H,5-6,9-18,20,38H2,1H3,(H,39,41)(H,40,53)(H,42,50)(H,43,51)(H,44,52)(H,48,49)(H,55,56)/t24-,25-,26-,27-,28-,29-/m0/s1
2.1.3 InChI Key
AFEHBIGDWIGTEH-AQRCPPRCSA-N
2.2 Other Identifiers
2.2.1 UNII
I5FAL2585H
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Acth (4-7), Pro-gly-pro-

2. Acth (4-7), Prolyl-glycyl-proline-

3. Pro-gly-pro-acth (4-7)

2.3.2 Depositor-Supplied Synonyms

1. 80714-61-0

2. Acth (4-7), Pro-gly-pro-

3. Mehfpgp

4. Met-glu-his-phe-pro-gly-pro

5. I5fal2585h

6. Acth (4-7), Prolyl-glycyl-proline-

7. Pro-gly-pro-acth (4-7)

8. Unii-i5fal2585h

9. L-methionyl-l-alpha-glutamyl-l-histidyl-l-phenylalanyl-l-prolylglycyl-l-proline

10. (2s)-1-[2-[[(2s)-1-[(2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-amino-4-methylsulfanylbutanoyl]amino]-4-carboxybutanoyl]amino]-3-(1h-imidazol-5-yl)propanoyl]amino]-3-phenylpropanoyl]pyrrolidine-2-carbonyl]amino]acetyl]pyrrolidine-2-carboxylic Acid

11. L-proline, 1-(n-(1-(n-(n-(n-l-methionyl-l-alpha-glutamyl)-l-histidyl)-l-phenylalanyl)-l-prolyl)glycyl)-

12. Semax?

13. H-met-glu-his-phe-pro-gly-pro-oh

14. Schembl7200319

15. Glxc-25922

16. Hy-p1146

17. Akos040744795

18. At42448

19. Da-77788

20. Met-glu-his-phe-pro-gly-pro [who-dd]

21. Cs-0028296

22. Methionyl-glutamyl-histidyl-phenylalanyl-prolyl-glycyl-proline

23. L-proline, L-methionyl-l-.alpha.-glutamyl-l-histidyl-l-phenylalanyl-l-prolylglycyl-

24. L-proline, L-methionyl-l-alpha-glutamyl-l-histidyl-l-phenylalanyl-l-prolylglycyl-

2.4 Create Date
2006-10-25
3 Chemical and Physical Properties
Molecular Weight 813.9 g/mol
Molecular Formula C37H51N9O10S
XLogP3-2.8
Hydrogen Bond Donor Count8
Hydrogen Bond Acceptor Count13
Rotatable Bond Count21
Exact Mass Da
Monoisotopic Mass Da
Topological Polar Surface Area312
Heavy Atom Count57
Formal Charge0
Complexity1450
Isotope Atom Count0
Defined Atom Stereocenter Count6
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Enzyme Inhibitors

Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. (See all compounds classified as Enzyme Inhibitors.)


Neuroprotective Agents

Drugs intended to prevent damage to the brain or spinal cord from ischemia, stroke, convulsions, or trauma. Some must be administered before the event, but others may be effective for some time after. They act by a variety of mechanisms, but often directly or indirectly minimize the damage produced by endogenous excitatory amino acids. (See all compounds classified as Neuroprotective Agents.)


Nootropic Agents

Drugs used to specifically facilitate learning or memory, particularly to prevent the cognitive deficits associated with dementias. These drugs act by a variety of mechanisms. (See all compounds classified as Nootropic Agents.)