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910228-13-6

910228-13-6 Structure

910228-13-6 Structure
IdentificationBack Directory
[Name]

Palmitoleoyl 3-carbacyclic Phosphatidic Acid
[CAS]

910228-13-6
[Synonyms]

IAGUMCXYAAGWJD-FPLPWBNLSA-N
Palmitoleoyl 3-carbacyclic Phosphatidic Acid
Palmitoleoyl 3-carbacyclic Phosphatidic Acid Exclusive
9-Hexadecenoic acid, (2-hydroxy-2-oxido-1,2-oxaphospholan-5-yl)methyl ester, (9Z)-
[Molecular Formula]

C20H37O5P
[MDL Number]

MFCD18427963
[MOL File]

910228-13-6.mol
[Molecular Weight]

388.48
Chemical PropertiesBack Directory
[solubility ]

PBS (pH 7.2): 5 mg/ml
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS06,GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H225-H302-H310-H331-H315-H319-H351-H361-H372
[Precautionary statements ]

P201-P202-P210-P240-P241-P242-P243-P260-P262-P264-P270-P271-P280-P301+P312-P303+P361+P353-P304+P340-P305+P351+P338-P310-P308+P313-P321-P314-P330-P361+P364-P332+P313-P337+P313-P370+P378-P403+P233-P403+P235-P405-P501
Hazard InformationBack Directory
[Description]

Cyclic phosphatidic acids (cPAs) are naturally occurring analogs of lysophosphatidic acid (LPA) in which the sn-2 hydroxy group forms a 5-membered ring with the sn-3 phosphate.1,2 Carba-derivatives of cPA (ccPA) are modified at the sn-2 (2-ccPA) or sn-3 (3-ccPA) linkage, preventing the opening of cPA to produce lysophosphatidic acid (LPA).3 Palmitoleoyl 3-carbacyclic phosphatidic acid (3-ccPA 16:1) is a cyclic LPA analog that contains the 16:1 fatty acid, palmitoleate, at the sn-1 position of the glycerol backbone.3 At 25 μM, it inhibits the transcellular migration of MM1 cells across mesothelial cell monolayers in response to fetal bovine serum (86.9%) or LPA (99.9%) without affecting proliferation.3 3-ccPA 16:1 significantly inhibits autotaxin (IC50 = 620 nM),4 an enzyme that is important in cancer cell survival, growth, migration, invasion and metastasis. When delivered intraperitoneally, 3-ccPA 16:1 significantly reduces the number of lung metastases formed in mice injected with B16F10 melanoma cells in the tail vein.4
[References]

1. Kobayashi, T., Tanaka-Ishii, R., Taguchi, R., et al. Existence of a bioactive lipid, cyclic phosphatidic acid, bound to human serum albumin Life Sci. 65(21),2185-2191(1999).
2. Mukai, M., Imamura, F., Ayaki, M., et al. Inhibition of tumor invasion and metastasis by a novel lysophosphatidic acid (cyclic LPA) Int. J. Cancer 81,918-922(1999).
3. Uchiyama, A., Mukai, M., Fujiwara, Y., et al. Inhibition of transcellular tumor cell migration and metastasis by novel carba-derivatives of cyclic phosphatidic acid Biochim. Biophys. Acta 1771,103-112(2007).
4. Baker, D.L., Fujiwara, Y., Pigg, K.R., et al. Carba analogs of cyclic phosphatidic acid are selective inhibitors of autotaxin and cancer cell invasion and metastasis J. Biol. Chem. 281(32),22786-22793(2006).
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