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Leptomycin B - 98%, high purity , CAS No.87081-35-4

  • ≥98%
Item Number
L102387
Grouped product items
SKUSizeAvailabilityPrice Qty
L102387-1mg
1mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$256.90
L102387-10mg
10mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,744.90

Discover Leptomycin B by Aladdin Scientific in 98% for only $256.90. Available - in Ligands at Aladdin Scientific. Antibiotic, antifungal. Inhibitor of CRM-1 mediated nuclear export. Tags: .

Basic Description

SynonymsLeptomycin B|Elactocin|Mantuamycin|87081-35-4|Antibiotic CI 940|Antibiotic CL 1957A|CI-940|LEPTOMYCIN B FROM STREPTOMYCES SP|CHEBI:52646|PD 114720|antibiotic ATS 1287B|Antibiotic PD 114720|Y031I2N1EO|ATS 1287B|CL-1957A|NSC-364372|LMB|PD-114720|(2E,5S,6R,7
Specifications & Purity98%
Storage TempProtected from light,Store at -20°C,Argon charged
Shipped InDry ice
Product Description

Leptomycin B is an anti-fungal antibiotic, anti-tumor cytotoxin that inhibits CRM1-dependent, NES-dependent nucleo-cytoplasmic translocation (nuclear export inhibitor). NES containing proteins include HIV-1 REV; actin, c-Abl, cyclin B1, MDM2/p53, IB, MPF, PKA and MEK.
Leptomycin B is a potent and specific nuclear export inhibitor. Leptomycin B alkylates and inhibits CRM1 (chromosomal region maintenance)/exportin 1, a protein required for nuclear export of proteins containing a nuclear export sequence (NES). In addition to antifungal and antibacterial activities, Leptomycin B blocks the cell cycle and is a potent anti-tumor agent. At low nM concentrations, Leptomycin B blocks the nuclear export of many proteins including HIV-1 Rev, MAPK/ERK, and NF-κB/IκB, and it stabilizes the expression of p53. Leptomycin B also inhibits the export and translation of many RNAs, including COX-2 and c-Fos mRNAs, by inhibiting export of ribonucleoproteins.

Associated Targets

XPO1 Tclin Exportin-1 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name (2E,5S,6R,7S,9R,10E,12E,15R,16Z,18E)-17-ethyl-6-hydroxy-3,5,7,9,11,15-hexamethyl-19-[(2S,3S)-3-methyl-6-oxo-2,3-dihydropyran-2-yl]-8-oxononadeca-2,10,12,16,18-pentaenoic acid
INCHI InChI=1S/C33H48O6/c1-9-28(14-15-29-24(5)13-16-31(36)39-29)19-22(3)12-10-11-21(2)17-25(6)32(37)27(8)33(38)26(7)18-23(4)20-30(34)35/h10-11,13-17,19-20,22,24-27,29,33,38H,9,12,18H2,1-8H3,(H,34,35)/b11-10+,15-14+,21-17+,23-20+,28-19-/t22-,24+,25-,26+,27-,29+,33-/m1/s1
InChi Key YACHGFWEQXFSBS-XYERBDPFSA-N
Canonical SMILES CCC(=CC(C)CC=CC(=CC(C)C(=O)C(C)C(C(C)CC(=CC(=O)O)C)O)C)C=CC1C(C=CC(=O)O1)C
Isomeric SMILES CC/C(=C/[C@H](C)C/C=C/C(=C/[C@@H](C)C(=O)[C@@H](C)[C@@H]([C@@H](C)C/C(=C/C(=O)O)/C)O)/C)/C=C/[C@H]1[C@H](C=CC(=O)O1)C
WGK Germany 1
PubChem CID 6917907
UN Number 1230
Molecular Weight 540.73

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Lot NumberCertificate TypeDateItem
L2206349Certificate of AnalysisNov 04, 2022 L102387

Chemical and Physical Properties

SolubilitySoluble in ethanol or methanol. Ethanol is recommended. Unstable in DMSO
SensitivityMoisture sensitive,Light sensitive
Flash Point(°F)64.4 °F
Flash Point(°C)18 °C

Safety and Hazards(GHS)

WGK Germany 1

Related Documents

References

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