Top Suppliers:I want be here
  • DC Chemicals Limited
  • China
  • Product Name: DSRM-3716
  • Price: ￥Inquiry/100mg ￥Inquiry/250mg ￥Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 10 Day
  • Contact: Tony Cao
Related CAS#:
58142-99-7 1151813-61-4
63986-53-8 956823-99-7
69207-52-9 2411308-32-0
1158522-08-7 2742006-38-6
940364-43-2 134104-43-1
131615-57-1 6906-52-1
930439-75-1 1018584-77-4
302923-02-0

58142-99-7

58142-99-7 structure
58142-99-7 structure
  • Name: DSRM-3716
  • Chemical Name: 5-Iodoisoquinoline
  • CAS Number: 58142-99-7
  • Molecular Formula: C9H6IN
  • Molecular Weight: 255.06
  • Catalog: Research Areas Neurological Disease
  • Create Date: 2018-05-22 08:00:00
  • Modify Date: 2024-01-06 19:41:55
  • DSRM-3716 (5-Iodoisoquinoline) is a potent and selective SARM1 NADase inhibitor with an IC50 of 75 nM. DSRM-3716 is selective against other NAD+-processing enzymes, receptors, and transporters. DSRM-3716 provides robust axon protection[1].
Name 5-Iodoisoquinoline
Synonyms 5-Iodoisoquinoline
Isoquinoline, 5-iodo-
Isoquinoline,5-iodo
5-iodo-isoquinoline
5-Jod-isochinolin
Description DSRM-3716 (5-Iodoisoquinoline) is a potent and selective SARM1 NADase inhibitor with an IC50 of 75 nM. DSRM-3716 is selective against other NAD+-processing enzymes, receptors, and transporters. DSRM-3716 provides robust axon protection[1].
Related Catalog
Target

IC50: 75 nM (SARM1 NADase)[1]

In Vitro DSRM-3716 treatment produces dose-dependent inhibition of cADPR increase (IC50 of 2.8 μM) and substantial preservation of NAD+ in these cultures in a manner consistent with engagement and inhibition of SARM1 enzymatic NADase activity inside the cells[1]. DSRM-3716 prevents neurofilament light chain (NfL) release from severed axons in a dose-dependent manner, with an IC50 of ~2 μM[1]. The potency of DSRM-3716 to inhibit cADPR increase caused by axotomy (IC50 of 2.8 μM) is similar to the potency required to prevent axonal degeneration (IC50 of 2.1 μM)[1]. DSRM-3716 inhibits the SARM1-dependent cell destruction pathway triggered by Rotenone in sensory neurons[1].
References

[1]. Robert O Hughes, et al. Small Molecule SARM1 Inhibitors Recapitulate the SARM1 -/- Phenotype and Allow Recovery of a Metastable Pool of Axons Fated to Degenerate. Cell Rep. 2021 Jan 5;34(1):108588.
Density 1.8±0.1 g/cm3
Boiling Point 336.8±15.0 °C at 760 mmHg
Molecular Formula C9H6IN
Molecular Weight 255.06
Flash Point 157.5±20.4 °C
Exact Mass 254.954483
PSA 12.89000
LogP 2.99
Vapour Pressure 0.0±0.7 mmHg at 25°C
Index of Refraction 1.724
Storage condition 2-8°C
Hazard Codes Xi
1125-60-6 structure

1125-60-6

~78%

58142-99-7 structure

58142-99-7

Literature: Gamage, Swarna A.; Spicer, Julie A.; Rewcastle, Gordon W.; Milton, John; Sohal, Sukhjit; Dangerfield, Wendy; Mistry, Prakash; Vicker, Nigel; Charlton, Peter A.; Denny, William A. Journal of Medicinal Chemistry, 2002 , vol. 45, # 3 p. 740 - 743
34784-04-8 structure

34784-04-8

~77%

58142-99-7 structure

58142-99-7

Literature: Hamad Elgazwy, Abdel-Sattar S. Phosphorus, Sulfur and Silicon and Related Elements, 2000 , vol. 164, p. 131 - 143
119-65-3 structure

119-65-3

~%

58142-99-7 structure

58142-99-7

Literature: Hamad Elgazwy, Abdel-Sattar S. Phosphorus, Sulfur and Silicon and Related Elements, 2000 , vol. 164, p. 131 - 143

Chemsrc provides CAS#:58142-99-7 MSDS, density, melting point, boiling point, structure, formula, molecular weight, synthetic route, etc.
title: CAS No. 58142-99-7 | Chemsrc address: https://www.chemsrc.com/en/baike/526144.html

Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer

Copyright © 2024 ChemSrc All Rights Reserved