- CAS
- Purity
- 149402-51-7
- 99%
Quality products?make an important contribution to long-term revenue and profitability. Manufacturer Supply Best Quality 14-Ethyl-9-(1-(hexyloxy)ethyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbine propanoic acid 149402-51-7 with Efficient Transportation
Photochlor is an anticancer photodynamic therapy drug that triggers multiple drug release and tumor killing cells in mouse breast cancer xenograft. Also functions as a photochlor-mediated photodynamic therapy for non-small cellular lung cancer treatment in murine model.
The CAS number of 14-Ethyl-9-(1-(hexyloxy)ethyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbine propanoic acid is 149402-51-7.
More information of 14-Ethyl-9-(1-(hexyloxy)ethyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbine propanoic acid 149402-51-7 are:
|
CAS?Number |
149402-51-7 |
|
Density |
1.24g/cm3 |
|
Boiling Point |
980.8°Cat760mmHg |
|
Flash Point |
547°C |
|
Vapor Pressure |
0mmHg at 25°C |
|
Refractive Index |
1.62 |
|
PSA |
119.57000 |
|
LogP |
5.99500 |
Synonyms?for?14-Ethyl-9-(1-(hexyloxy)ethyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbine propanoic acid 149402-51-7:2-[1'-(Hexyloxy)ethyl]-2-devinylpyropheophorbidea; 3-Devinyl-3-(1'-hexyloxy)ethylpyropheophorbide A;3-[1'-(Hexyloxy)ethyl]-3-devinylpyropheophorbide a; HPPH; Photochlor
The chemical formula of ?14-Ethyl-9-(1-(hexyloxy)ethyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbine propanoic acid is?C39H48 N4 O4 which containing 39 Carbon atoms,48 Hydrogen atoms,4 Nitrogen atoms and 4 Oxygen atoms,and the molecular weight of??14-Ethyl-9-(1-(hexyloxy)ethyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbine propanoic acid?is 636.82.
HPPH is a chlorin that acts as a photosensitizer in photodynamic therapy (PDT) when stimulated with light at 655 nm. When administered systemically, HPPH accumulates in tumor cells and, when stimulated with light in the presence of oxygen, reactive oxygen species (ROS) are generated, leading to necrosis within the tumor. HPPH, at a dose of 0.5 mg/kg, increases survival in a nude rat model of glioma. It works synergistically with gemcitabine in several pancreatic cancer cell lines to induce cell death.
InChI:InChI=1/C39H48N4O4/c1-8-10-11-12-15-47-24(7)36-22(5)30-17-29-21(4)26(13-14-35(45)46)38(42-29)27-16-34(44)37-23(6)31(43-39(27)37)18-32-25(9-2)20(3)28(40-32)19-33(36)41-30/h17-19,21,24,26,40-41H,8-16H2,1-7H3,(H,45,46)/b28-19-,29-17-,30-17-,31-18-,32-18-,33-19-,38-27-/t21-,24?,26-/m0/s1
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