| Weight | 482.324 g/mol |
|---|---|
| Formula | C18H36Cl4N4O2 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
Prospidine (23476-83-7)
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- Prospidine versus methotrexate pulse in highly active rheumatoid arthritis: A controlled 6-month clinical trial (Clinical Rheumatology, 1994)
- Effects of Prospidine on Survival and Growth of Mammalian Cells in Culture (Journal of the National Cancer Institute, 1980)
- Clinical use of prospidine (Voprosy onkologii, 1970)
- Preparation and Antitumor Activity of a Gel-Forming Prospidine Formulation (Pharmaceutical Chemistry Journal, 2013)
- Overadditive chemotherapeutic synergism of prospidine and inosine when given sequentially to the sarcoma 180 implanted intramuscularly (Journal of Cancer Research and Clinical Oncology, 1980)
- Effect of prospidine administered at different times of the day on the development and growth of N-nitrosomethylurea-induced mammary tumors in Wistar rats (Cancer Letters, 1984)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C[N+]2(CCN1CC(CCl)O)CC[N+]3(CCN(CC3)CC(CCl)O)CC2.[Cl-].[Cl-]
-
InChIKeyQZJPEEOEZVHUAE-UHFFFAOYSA-L
- Pubchem - Prospidine
- Wikipedia - prospidium chloride
Prospidium chloride (prospidine) is a drug with cytostatic (alkylating) and anti-inflammatory properties. It has been studied for the treatment of rheumatoid arthritis. Chemically, it is a spiro compound.
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