Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C99H155N29O21S |
Molecular Weight | 2119.537 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 14 / 14 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CSCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)CCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC2=CNC=N2)C(=O)N[C@@H](CC3=CC=CC=C3)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC4=CNC5=C4C=CC=C5)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N6CCC[C@H]6C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)NCCCCN
InChI
InChIKey=DIDCGVRALANKIU-OTEFFYEFSA-N
InChI=1S/C99H155N29O21S/c1-59(2)84(97(148)113-56-81(132)115-68(26-10-14-40-101)87(138)119-69(27-11-15-41-102)88(139)118-67(25-9-13-39-100)85(136)109-45-18-17-43-104)127-96(147)79-30-20-47-128(79)98(149)73(28-12-16-42-103)116-82(133)55-112-86(137)76(51-62-53-111-66-24-8-7-23-65(62)66)124-89(140)70(29-19-46-110-99(106)107)120-93(144)75(49-60-21-5-4-6-22-60)123-94(145)77(52-63-54-108-58-114-63)125-90(141)71(35-36-83(134)135)121-91(142)72(38-48-150-3)122-95(146)78(57-129)126-92(143)74(117-80(131)37-44-105)50-61-31-33-64(130)34-32-61/h4-8,21-24,31-34,53-54,58-59,67-79,84,111,129-130H,9-20,25-30,35-52,55-57,100-105H2,1-3H3,(H,108,114)(H,109,136)(H,112,137)(H,113,148)(H,115,132)(H,116,133)(H,117,131)(H,118,139)(H,119,138)(H,120,144)(H,121,142)(H,122,146)(H,123,145)(H,124,140)(H,125,141)(H,126,143)(H,127,147)(H,134,135)(H4,106,107,110)/t67-,68-,69-,70-,71-,72-,73-,74-,75-,76-,77-,78-,79-,84-/m0/s1
Molecular Formula | C99H155N29O21S |
Molecular Weight | 2119.537 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 14 / 14 |
E/Z Centers | 10 |
Optical Activity | UNSPECIFIED |
Alsactide (Synchrodyn) is synthesized heptadecapeptide analog of adrenocorticotropic hormone (ACTH) having a C-terminal amide group (butylamide) and the substitution of beta-alanine for serine in position 1 and of lysine for arginine in position 17. These modifications account for enhanced biological activity and uniquely demonstrated chronopharmacological properties. In adult healthy men, the tailoring of dosage and timing of peptide administration was successful in a selective and transient stimulation of glucocorticoid secretion, without a change in the plasma concentrations of aldosterone and testosterone. The clinical use of alsactide has provided new diagnostic information about subtle alterations of the adrenal function and has been valuable to presenting the rhythmic ordering of several functions, especially of those which are more dependent on the glucocorticoid modulation.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3040344
10 ug
Route of Administration:
Other
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:21:02 GMT 2023
by
admin
on
Sat Dec 16 01:21:02 GMT 2023
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Record UNII |
J0K70H3420
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Code | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Classification Tree | Code System | Code | ||
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WHO-VATC |
QV04CH04
Created by
admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
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WHO-ATC |
V04CH04
Created by
admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
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Code System | Code | Type | Description | ||
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139
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16129705
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C169775
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34765-96-3
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100000087493
Created by
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PRIMARY | |||
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DTXSID90188321
Created by
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m1580
Created by
admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
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PRIMARY | Merck Index | ||
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Alsactide
Created by
admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
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252-203-0
Created by
admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
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J0K70H3420
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CHEMBL2104374
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DB13298
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SUB05374MIG
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4965
Created by
admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ACTIVE MOIETY |