Skip to Content
Merck
CN

K1513

Kendomycin from Streptomyces violaceoruber

solid

Synonym(s):

(−)-TAN 2162

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C29H42O6
CAS Number:
183202-73-5
Molecular Weight:
486.64
NACRES:
NA.77
PubChem Substance ID:
24896208
UNSPSC Code:
12352202
MDL number:
MFCD00076711

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI

1S/C32H61N13O9/c1-15(2)13-19(33)25(48)42-21(10-8-12-39-32(36)37)27(50)43-20(9-7-11-38-31(34)35)26(49)40-17(5)24(47)44-22(14-46)28(51)45-23(16(3)4)29(52)41-18(6)30(53)54/h15-23,46H,7-14,33H2,1-6H3,(H,40,49)(H,41,52)(H,42,48)(H,43,50)(H,44,47)(H,45,51)(H,53,54)(H4,34,35,38)(H4,36,37,39)

SMILES string

CC(C)CC(N)C(=O)NC(CCCNC(N)=N)C(=O)NC(CCCNC(N)=N)C(=O)NC(C)C(=O)NC(CO)C(=O)NC(C(C)C)C(=O)NC(C)C(O)=O

InChI key

PPBZOEOSJVJLRX-UHFFFAOYSA-N

form

solid

antibiotic activity spectrum

Gram-negative bacteria, Gram-positive bacteria, neoplastics

mode of action

protein synthesis | interferes

storage temp.

−20°C

Quality Level

200

General description

Chemical structure: peptide

Biochem/physiol Actions

Potent endothelin receptor antagonist. Antiosteoporotic compound. Shows also remarkable antibacterial and cytotoxic activity. A putative cellular target for cytotoxicity has been identified: inhibition or altered regulation of the proteasome.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
126K1423
096K1421
036K1231
125K1584
083K1073

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Structure and biosynthesis of kendomycin, a carboxylic ansa-compound from Streptomyces. .
Zeeck, A. , and Bode, H.B.
Journal of the Chemical Society. Perkin Transactions 1, 323-323 (2000)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service