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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
Structure of ALSACTIDE

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

HIDE SMILES / InChI

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

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct

Sample Use Guides

10 ug
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:21:02 GMT 2023
Edited
by admin
on Sat Dec 16 01:21:02 GMT 2023
Record UNII
J0K70H3420
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ALSACTIDE
INN   MI   WHO-DD  
INN  
Official Name English
HOE-433
Code English
ALSACTIDE [MI]
Common Name English
alsactide [INN]
Common Name English
.ALPHA.1-17-CORTICOTROPIN, 1-.BETA.-ALANINE-17-(N-(4-AMINOBUTYL)-L-LYSINAMIDE)-
Systematic Name English
ALISACTIDE
Common Name English
.ALPHA.1-17-CORTICOTROPIN, 1-.BETA.-ALANINE-17-(L-2,6-DIAMINO-N-(4-AMINOBUTYL)HEXANAMIDE)-
Systematic Name English
1-.BETA.-ALANINE-17-(L-2,6-DIAMINO-N-(4-AMINOBUTYL)HEXANAMIDE)-.ALPHA.(SUP 1,17)-CORTICOTROPIN
Common Name English
Alsactide [WHO-DD]
Common Name English
SYNCHRODYN
Brand Name English
Classification Tree Code System Code
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
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
Code System Code Type Description
DRUG CENTRAL
139
Created by admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
PRIMARY
PUBCHEM
16129705
Created by admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
PRIMARY
NCI_THESAURUS
C169775
Created by admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
PRIMARY
CAS
34765-96-3
Created by admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
PRIMARY
SMS_ID
100000087493
Created by admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
PRIMARY
EPA CompTox
DTXSID90188321
Created by admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
PRIMARY
MERCK INDEX
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
PRIMARY Merck Index
WIKIPEDIA
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
PRIMARY
ECHA (EC/EINECS)
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
PRIMARY
FDA UNII
J0K70H3420
Created by admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104374
Created by admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
PRIMARY
DRUG BANK
DB13298
Created by admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
PRIMARY
EVMPD
SUB05374MIG
Created by admin on Sat Dec 16 01:21:02 GMT 2023 , Edited by admin on Sat Dec 16 01:21:02 GMT 2023
PRIMARY
INN
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
PRIMARY
Related Record Type Details
ACTIVE MOIETY