추천 제품
Quality Level
분석
98%
광학 활성
[α]20/D −40°, c = 1.0 in ethanol
반응 적합성
reaction type: solution phase peptide synthesis
mp
169-172 °C (lit.)
응용 분야
peptide synthesis
SMILES string
O[C@H]([C@@H](NC(=O)c1ccccc1)c2ccccc2)C(O)=O
InChI
1S/C16H15NO4/c18-14(16(20)21)13(11-7-3-1-4-8-11)17-15(19)12-9-5-2-6-10-12/h1-10,13-14,18H,(H,17,19)(H,20,21)/t13-,14+/m0/s1
InChI key
HYJVYOWKYPNSTK-UONOGXRCSA-N
애플리케이션
The presence of this chiral side chain has proven to be essential for the biological activity of taxol, one of the most promising anticancer agents being investigated. The challenging synthesis of taxol has stimulated interest in the attachment of the C-13 side chain to naturally derived taxanes like baccatin III.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 9(9), 1692-1703 (1991-09-01)
Untreated and minimally pretreated solid tumor patients received alternating sequences of taxol and cisplatin. Sequential dose escalation of each agent using taxol doses of 110 or 135 mg/m2 and cisplatin doses of 50 or 75 mg/m2 resulted in four dosage
Tetrahedron, 45, 4177-4177 (1989)
Tetrahedron Letters, 34, 4149-4149 (1993)
Journal of the American Chemical Society, 116, 1597-1597 (1994)
Taxol: twenty years later, the story unfolds.
Journal of the National Cancer Institute, 83(24), 1778-1781 (1991-12-18)
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