Phthalocyanine

CAS : 574-93-6

Ref. 3D-FP41169

Informations sur le produit

• Nom: Phthalocyanine
• Synonymes: (1Z,10Z,19Z,29Z)-2,11,20,37,38,39,40-heptaazanonacyclo[28.6.1.1~3,10~.1~12,19~.1~21,28~.0~4,9~.0~13,18~.0~22,27~.0~31,36~]tetraconta-1,3(40),4,6,8,10,12(39),13,15,17,19,21,23,25,27,29,31,33,35-nonadecaene (non-preferred name), 29H,30H-Tetrabenzo[b,g,l,q]porphine, 29H,30H-phthalocyanine, 29H,31H-Phtalocyanine, 29H,31H-Phthalocyanin, 29H,31H-ftalocianina, 5,28:14,19-Diimino-7,12:26,21-dinitrilotetrabenzo[c,h,m,r][1,6,11,16]tetraazacycloeicosine, 74100, 8120S, Blue Pigment B, Cg 1-1, Fastogen Blue 8110, Fastogen Blue 8120, Fastogen Blue 8120B, Fastogen Blue 8120BS, Fastogen Blue 8130, Fastogen Blue GS, H2Pc, Heliogen Blue 7560, Heliogen Blue 7565, Heliogen Blue 7800, Heliogen Blue D 7490, Heliogen Blue D 7560, Heliogen Blue D 7565, Heliogen Blue G, Heliogen Blue L 7460, Heliogen Blue L 7560, Heliogen Blue LG, Irgalite Blue GLS, Irgazin Blue 3GT, Lionol Blue KW, Liophoton, Liophoton THP, Liophoton TPA 891, Lt-N222, Mcp 80, Monastral Fast Blue G, Monolite Fast Blue GS, Na 570, P 0355, P.B.16, PV-Fast Blue G, Pb 16, Photo Fine TPA 891, Phthalo Blue (Metal free), Pigment Blue 16, Pigment Blue Green Phthalocyanine U, Polymon Blue G, Progen I, Tetrabenzo[b,g,l,q]porphine, Tetrabenzo[b,g,l,q]porphyrazine, Tetrabenzoporphyrazine, Tetrabenzotetraazaporphine, Tpa 891, Vulcafor Fast Blue G, Vulcanosine Fast Bremen Blue G, Vynamon Blue G, χ-Phthalocyanine
• CAS: 574-93-6

Description

Phthalocyanine is a molecule that shows antimicrobial properties. It has been shown to inhibit the growth of bacteria, fungi, and yeast by inhibiting the synthesis of DNA. In vitro assays have been used to demonstrate the antibacterial activity of phthalocyanines against Gram-positive and Gram-negative bacteria. The mechanism of action involves binding to the bacterial cell membrane, which blocks the uptake of phosphate ions. This leads to inhibition of phospholipid synthesis, causing cell death. Phthalocyanine also exhibits anticancer activity in vitro and in vivo models. It inhibits skin cancer cells by binding to metal chelates that are present in these cells and then reacting with oxygen radicals. These reactions lead to DNA damage and apoptosis (cell death).

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 514.54 g/mol
• Formule: C₃₂H₁₈N₈
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C32H18N8/c1-2-10-18-17(9-1)25-33-26(18)38-28-21-13-5-6-14-22(21)30(35-28)40-32-24-16-8-7-15-23(24)31(36-32)39-29-20-12-4-3-11-19(20)27(34-29)37-25/h1-16H,(H2,33,34,35,36,37,38,39,40)
• Code InChI: InChIKey=IEQIEDJGQAUEQZ-UHFFFAOYSA-N
• SMILES: c1ccc2c(c1)-c1nc-2nc2[nH]c(nc3nc(nc4[nH]c(n1)c1ccccc41)-c1ccccc1-3)c1ccccc21