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ACTH (1-10) is a synthetic peptide consisting of the first ten amino acids of the adrenocorticotropic hormone (ACTH). It is involved in the regulation of steroid hormone production and release in the adrenal glands, particularly cortisol. This peptide is commonly utilized in laboratory research to investigate the physiological effects and signaling pathways of the full-length ACTH hormone.
Used in Pharmaceutical Research:
ACTH (1-10) is used as a research tool for studying the physiological effects and signaling pathways of the full-length ACTH hormone, aiding in the understanding of adrenal gland function and the regulation of steroid hormones.
Used in Laboratory Research:
ACTH (1-10) is used as a research compound to explore its potential therapeutic applications in treating conditions such as adrenal insufficiency and related disorders, providing insights into the development of new treatments for these conditions.
Used in Immunology and Inflammation Studies:
ACTH (1-10) is used as a modulator of immune response and inflammation, being investigated for its role in these processes, which could lead to the development of pharmaceuticals targeting immune-related conditions.
Used in Drug Development:
ACTH (1-10) is considered a promising target for pharmaceutical development in the future, with potential applications in treating adrenal insufficiency and modulating immune responses, based on its effects on the adrenal glands and immune system.

2791-05-1

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2791-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2791-05-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,9 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2791-05:
(6*2)+(5*7)+(4*9)+(3*1)+(2*0)+(1*5)=91
91 % 10 = 1
So 2791-05-1 is a valid CAS Registry Number.
InChI:InChI=1/C59H78N16O16S/c1-92-21-19-42(70-58(91)47(30-77)75-56(89)43(71-50(83)38(60)29-76)23-33-13-15-36(78)16-14-33)54(87)69-41(17-18-48(79)80)53(86)74-46(25-35-27-63-31-67-35)57(90)72-44(22-32-8-3-2-4-9-32)55(88)68-40(12-7-20-64-59(61)62)52(85)73-45(51(84)66-28-49(81)82)24-34-26-65-39-11-6-5-10-37(34)39/h2-6,8-11,13-16,26-27,31,38,40-47,65,76-78H,7,12,17-25,28-30,60H2,1H3,(H,63,67)(H,66,84)(H,68,88)(H,69,87)(H,70,91)(H,71,83)(H,72,90)(H,73,85)(H,74,86)(H,75,89)(H,79,80)(H,81,82)(H4,61,62,64)/t38-,40-,41-,42-,43-,44-,45-,46-,47-/m0/s1

2791-05-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ACTH (1-10)

1.2 Other means of identification

Product number -
Other names ADRENOCORTICOTROPIC HORMONE (1-14)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2791-05-1 SDS

2791-05-1Upstream product

2791-05-1Downstream Products

2791-05-1Relevant academic research and scientific papers

MODIFICATION OF TRYPTOPHAN RESIDUES DURING ACIDOLYSIS OF 4-METHOXY-2,3,6-TRIMETHYLBENZENESULFONYL GROUPS. EFFECTS OF SCAVENGERS

Sieber, Peter

, p. 1637 - 1640 (1987)

The formation of by-product 1 of tryptophan during the cleavage of Mtr from arginine can be minimized by addition of 1,2-ethanedithiol.Under too drastic conditions, however, a dithioketal product 2 is formed.

SYNTHESIS OF FRAGMENTS OF THE ADRENOCORTICOTROPIC HORMONE (ACTH1-10, ACTH11-24, AND ACTH1-24) WITH THE USE OF A CHROMOGENIC C-TERMINAL PROTECTIVE GROUP LABILE TO ALKALI

Kalashnikov, V. V.,Polyakova, I. M.

, p. 971 - 974 (2007/10/02)

A method for the fast synthesis of fragments of adrenocorticotropin (regions 1-10, 11-24, and 1-24 of the amino acid sequence of ACTH) has been developed which allows us to produce preparative quantities of these peptides.A colored 2-(4-phenylazobenzylsulfonyl)ethyl C-terminal protective group, removable by bases, was used in the synthesis.

APPLICATION OF THE NG-(2,2,5,7,8-PENTAMETHYLCHROMAN-6-SULPHONYL) DERIVATIVE OF FMOC-ARGININE TO PEPTIDE SYNTHESIS

Green, J.,Ogunjobi, O. M.,Ramage, R.,Stewart, A. S. J.

, p. 4341 - 4344 (2007/10/02)

The trifluoroacetic acid labile pentamethylchromanylsulphonyl protecting group for the guanidino group of arginine has been used in conjunction with the base-labile Fmoc Nα protecting group for the synthesis of arginine-containing peptides.

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