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INDEX NAME NOT YET ASSIGNED

CAS No.
2469263-61-2
Chemical Name:
INDEX NAME NOT YET ASSIGNED
Synonyms
N-Nitroso Sertraline-13CD315N
CBNumber:
CB210775781
Molecular Formula:
C10H13ClN2O
Molecular Weight:
212.68
MDL Number:
MOL File:
2469263-61-2.mol
Last updated:2024-07-02 08:55:01

INDEX NAME NOT YET ASSIGNED Properties

solubility Methanol: slightly soluble; Water: slightly soluble
form A solid
color Off-white to gray

SAFETY

Risk and Safety Statements

INDEX NAME NOT YET ASSIGNED price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 29415 Serotonin-d4 (hydrochloride) ≥99% deuterated forms (d1-d4) 2469263-61-2 1 mg $108 2024-03-01 Buy
Cayman Chemical 29415 Serotonin-d4 (hydrochloride) ≥99% deuterated forms (d1-d4) 2469263-61-2 5 mg $400 2024-03-01 Buy
Cayman Chemical 29415 Serotonin-d4 (hydrochloride) ≥99% deuterated forms (d1-d4) 2469263-61-2 10 mg $747 2024-03-01 Buy
Product number Packaging Price Buy
29415 1 mg $108 Buy
29415 5 mg $400 Buy
29415 10 mg $747 Buy

INDEX NAME NOT YET ASSIGNED Chemical Properties,Uses,Production

Description

Serotonin-d4 is intended for use as an internal standard for the quantification of serotonin by GC- or LC-MS. Serotonin is a monoamine neurotransmitter that is biochemically derived from tryptophan and produced in serotonergic neurons in the central nervous system and in enterochromaffin cells in the gastrointestinal tract.1,2,3,4 Serotonin is important in the regulation of mood, sleep, vomiting, sexuality, and appetite. Low levels of serotonin are associated with several disorders, including depression, migraines, bipolar disorder, and anxiety. Its actions are terminated primarily via uptake of serotonin from the synapse. Serotonin reuptake can be inhibited with MDMA, cocaine, tricyclic antidepressants, and selective serotonin reuptake inhibitors.

References

1. Martinez, A., Knappskog, P.M., and Haavik, J. A structural approach into human tryptophan hydroxylase and its implications for the regulation of serotonin biosyntheis Curr. Med. Chem. 8(9),1077-1091(2001).
2. Liu, Q., Yang, Q., Sun, W., et al. Discovery and characterization of novel tryptophan hydroxylase inhibitors that selectively inhibit serotonin synthesis in the gastrointestinal tract J. Pharmacol. Exp. Ther. 325(1),47-55(2008).
3. Schmid, C.L., and Bohn, L.M. Serotonin, but not N-methyltryptamines, activates the serotonin 2A receptor via a β-arrestin2/Src/Akt signaling complex in vivo J. Neurosci. 30(40),13513-13524(2010).
4. Berger, M., Gray, J.A., and Roth, B.L. The expanded biology of serotonin Annu. Rev. Med. 60,355-366(2009).

INDEX NAME NOT YET ASSIGNED Preparation Products And Raw materials

Raw materials

Preparation Products

INDEX NAME NOT YET ASSIGNED Suppliers

Global( 5)Suppliers
Supplier Tel Email Country ProdList Advantage
Artis Biotech Co. Ltd. 19138486554 18582380095 sales@artisbio.com China 2965 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 11975 58
Nanjing Shizhou Biology Technology Co.,Ltd 17301488900 judy.xia@synzest.com China 12582 58
Jiangsu Aikon Biopharmaceutical R&D Co.,Ltd. 025-66061636 18013972705 qqyang@aikonchem.com China 10238 58
N-Nitroso Sertraline-13CD315N 2469263-61-2