| Weight | 145.158 g/mol |
|---|---|
| Formula | C6H11NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
Methyl aminolevulinate (33320-16-0)
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- Photodynamic therapy using topical methyl 5-aminolevulinate compared with cryotherapy for actinic keratosis: A prospective, randomized study (Journal of The American Academy of Dermatology, 2002)
- Photodynamic therapy using topical methyl aminolevulinate vs surgery for nodular basal cell carcinoma - Results of a multicenter randomized prospective trial (Archives of Dermatology, 2004)
- Photodynamic therapy with topical methyl aminolevulinate for actinic keratosis: Results of a prospective randomized multicenter trial (Journal of The American Academy of Dermatology, 2003)
- A comparison of photodynamic therapy using topical methyl aminolevulinate (Metvix) with single cycle cryotherapy in patients with actinic keratosis: a prospective, randomized study (Journal of Dermatological Treatment, 2003)
- Selective distribution of porphyrins in skin thick basal cell carcinoma after topical application of methyl 5-aminolevulinate. (Journal of Photochemistry and Photobiology B-biology, 2001)
- A randomized multicenter study to compare two treatment regimens of topical methyl aminolevulinate (Metvix)-PDT in actinic keratosis of the face and scalp (Acta Dermato-venereologica, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)CCC(=O)CN
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InChIKeyYUUAYBAIHCDHHD-UHFFFAOYSA-N
- Pubchem - Methyl aminolevulinate
- Wikipedia - methyl aminolevulinate
Methyl aminolevulinate (MAL) is a drug used as a sensitizer in photodynamic therapy. It is a prodrug that is metabolized to protoporphyrin IX. It is marketed as Metvix.
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