ACV 1

ACV 1 Property

storage temp. 

Store at -20°C

solubility 

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.

form 

Powder

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H300Fatal if swallowed

H310Fatal in contact with skin

H330Fatal if inhaled

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P262Do not get in eyes, on skin, or on clothing.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P284Wear respiratory protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P302+P350IF ON SKIN: Gently wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P310Immediately call a POISON CENTER or doctor/physician.

P320Specific treatment is urgent (see … on this label).

P321Specific treatment (see … on this label).

P322Specific measures (see …on this label).

P330Rinse mouth.

P361Remove/Take off immediately all contaminated clothing.

P363Wash contaminated clothing before reuse.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

P405Store locked up.

P501Dispose of contents/container to..…

ACV 1 Chemical Properties,Usage,Production

Enzyme inhibitor

This neuronal nicotinic acetylcholine receptor antagonist (FW = 1806.98 g/mol; CAS 740980-24-9), also known as Conotoxin Vc1.1, is produced from mRNA in venom duct of Conus victoriae. ACV 1 selectively targets the α9α10 nAChR subtype (IC50 = 19 nM), with weaker action against α6/α3β2β3 (IC50 = 140 nM), α6/α3β4 (IC50 = 980 nM), α3β4 (IC50 = 4200 nM), and α3β2 (IC50 = 7300 nM) nAChR subtypes. ACV-1 suppresses vascular responses to unmyelinated sensory nerve C-fiber activation in rats, as related to pain transmission. ACV-1 and its posttranslationally modified analogues vc1a, [P6O]Vc1.1, and [E14g]Vc1.1 are equally potent at inhibiting ACh-evoked currents mediated by α9α10 nAChRs.