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Published TCIMAIL newest issue No.197
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CAS RN: 19685-09-7 | Product Number: H1463
10-Hydroxycamptothecin
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Purity: >98.0%(HPLC)
Synonyms:
Product Documents:
| Size | Unit Price | Belgium | Japan* | Quantity |
|---|---|---|---|---|
| 1G |
€162.00
|
1 | 2 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
| Product Number | H1463 |
| Purity / Analysis Method | >98.0%(HPLC) |
| Molecular Formula / Molecular Weight | C__2__0H__1__6N__2O__5 = 364.36 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Frozen (<0°C) |
| Condition to Avoid | Heat Sensitive |
| CAS RN | 19685-09-7 |
| Reaxys Registry Number | 3019077 |
| PubChem Substance ID | 354335739 |
| MDL Number | MFCD02093100 |
Specifications
| Appearance | White to Yellow to Orange powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(with Total Nitrogen) | min. 97.0 % |
Properties (reference)
| Melting Point | 267 °C |
| Specific Rotation | 35.3° (C=0.11,CH2Cl2:MeOH=4:1) |
| Maximum Absorption Wavelength | 382 nm |
GHS
| Pictogram |
|
| Signal Word | Danger |
| Hazard Statements | H301 + H311 + H331 : Toxic if swallowed, in contact with skin or if inhaled. |
| Precautionary Statements | P261 : Avoid breathing dust. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ protective clothing. P301 + P310 + P330 : IF SWALLOWED: Immediately call a POISON CENTER/doctor. Rinse mouth. P302 + P352 + P312 : IF ON SKIN: Wash with plenty of water. Call a POISON CENTER/doctor if you feel unwell. P403 + P233 : Store in a well-ventilated place. Keep container tightly closed. |
Related Laws:
| RTECS# | UQ0491700 |
Transport Information:
| UN Number | UN1544 |
| Class | 6.1 |
| Packing Group | III |
| HS Number | 2939799090 |
Application
10-Hydroxycamptothecin: An Inhibitor of Topoisomerase I with Antitumor Activity
10-hydroxycamptothecin (10-HCPT) is an inhibitor of topoisomerase I originally isolated from the Chinese tree C. acuminata. 10-HCPT, a member of the camptothecin family, interferes with DNA synthesis by inhibiting the enzyme topoisomerase-I, and has a broad spectrum of antitumor activity and less toxicity as a camptothecins.1,2) However, 10-HCPT is insoluble in both water and physiological acceptable organic solvents and tends to change into its carboxylate form, which shows minimal antitumor activity and several unpredictable side effects.3,4) Therefore, appropriate drug delivery systems (DDS) for 10-HPCT have been developed to improve the stability of its lactone form.5,6) 10-HCPT is also an important precursor for the synthesis of the clinical useful anticancer agents, such as irinotecan [I0714]. (The product is for research purpose only.)
References
- 1)Exploring DNA Topoisomerase I Ligand Space in Search of Novel Anticancer Agents
- 2)Synthesis and Preliminary Anticancer Evaluation of 10-Hydroxycamptothecin Analogs
- 3)Preparation, characterization and biodistribution of the lactone form of 10-hydroxycamptothecin (HCPT)-loaded bovine serum albumin (BSA) nanoparticles
- 4)Simultaneous determination of the carboxylate and lactone forms of 10-hydroxycamptothecin in human serum by restricted-access media high-performance liquid chromatography
- 5)10-Hydroxycamptothecin loaded nanoparticles: Preparation and antitumor activity in mice
- 6)Efficient tumor targeting of hydroxycamptothecin loaded PEGylated niosomes modified with transferrin
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