A2836
Ansamitocin P-3 from Actinosynnema pretiosum
≥90% (HPLC)
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关于此项目
经验公式（希尔记法）:
C32H43ClN2O9
化学文摘社编号:
分子量:
635.14
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352202
MDL number:
产品名称
Ansamitocin P-3 from Actinosynnema pretiosum, ≥90% (HPLC)
InChI
1S/C32H43ClN2O9/c1-17(2)29(37)43-25-15-26(36)35(6)21-13-20(14-22(40-7)27(21)33)12-18(3)10-9-11-24(41-8)32(39)16-23(42-30(38)34-32)19(4)28-31(25,5)44-28/h9-11,13-14,17,19,23-25,28,39H,12,15-16H2,1-8H3,(H,34,38)/b11-9+,18-10+/t19-,23+,24-,25+,28-,31+,32+/m1/s1
SMILES string
CO[C@@H]1\C=C\C=C(C)\Cc2cc(OC)c(Cl)c(c2)N(C)C(=O)C[C@H](OC(=O)C(C)C)[C@]3(C)O[C@@H]3[C@H](C)[C@@H]4C[C@@]1(O)NC(=O)O4
InChI key
OPQNCARIZFLNLF-KUDLRRJMSA-N
assay
≥90% (HPLC)
form
powder
storage temp.
2-8°C
Quality Level
Biochem/physiol Actions
Fungal metabolite with antineoplastic, antimitotic activity. Binds to tubulin and inhibits vinblastine-induced spiral formation.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Highly active ansamitocin derivatives: mutasynthesis using an AHBA-blocked mutant.
Florian Taft et al.
Chembiochem : a European journal of chemical biology, 9(7), 1057-1060 (2008-04-03)
Daniel Ng et al.
Journal of industrial microbiology & biotechnology, 36(11), 1345-1351 (2009-07-18)
Constitutive overexpression of regulators in the ansamitocin biosynthetic cluster of Actinosynnema pretiosum was investigated as a strategy to increase the production of ansamitocin-P3 (AP-3), a clinically promising chemotherapeutic agent. Putative transcriptional regulators asm2, asm29, and asm34 as well as the
Carl E Snipes et al.
Journal of natural products, 70(10), 1578-1581 (2007-09-26)
The ansacarbamitocins are a new family of maytansinoids that are unusually substituted with a glucose subunit and two carbamate functional groups and exhibit modest activity against some agricultural fungal disease organisms. Ansacarbamitocins A-F ( 1- 6) all consist of the
Yan Li et al.
Chemistry & biology, 18(12), 1571-1580 (2011-12-27)
Carbamoylation is one of the post-PKS modifications in ansamitocin biosynthesis. A novel ansamitocinoside with carbamoyl substitution at the C-4 hydroxyl group of the N-β-D-glucosyl moiety was identified from the ansamitocin producer, Actinosynnema pretiosum. Through biotransformation, the carbamoyltransferase gene asm21 was
Yuqin Yao et al.
Journal of separation science, 33(9), 1331-1337 (2010-03-18)
Ansamitocin P-3 is a potent anti-tumor maytansinoid found in Actinosynnema pretiosum. However, due to the complexity of the fermentation broth of Actinomycete, how to effectively separate ansamitocin P-3 is still a challenge. In this study, both analytical and preparative high-performance
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