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TetroMycin B

Product Name
TetroMycin B
CAS No.
180027-84-3
Chemical Name
TetroMycin B
Synonyms
TetroMycin B;18H-16a,19-Metheno-16aH-benzo[b]naphth[2,1-j]oxacyclotetradecin-18,20(1H)-dione, 2,3,4,4a,6a,9,10,12a,15,16,20a,20b-dodecahydro-4,21-trihydroxy-1,6,7,11,12a,14,15,20a-octamethyl-, (1S,4S,4aS,6aR,7E,11E,12aR,15R,16aS,20aS,20bR)- (9CI)
CBNumber
CB22703770
Molecular Formula
C34H46O5
Formula Weight
534.72604
MOL File
180027-84-3.mol
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TetroMycin B Property

Boiling point:
680.0±55.0 °C(Predicted)
Density 
1.17±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble
form 
A solid
pka
4.50±1.00(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
23766
Product name
Tetromycin B
Purity
≥99%
Packaging
500μg
Price
$255
Updated
2024/03/01
Cayman Chemical
Product number
23766
Product name
Tetromycin B
Purity
≥99%
Packaging
2.5mg
Price
$1143
Updated
2024/03/01
TRC
Product number
T309510
Product name
TetromycinB
Packaging
500μg
Price
$230
Updated
2021/12/16
Usbiological
Product number
T3530-05
Product name
Tetromycin B
Packaging
500ug
Price
$523
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0012606
Product name
TETROMYCIN B
Purity
95.00%
Packaging
5MG
Price
$498.32
Updated
2021/12/16
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TetroMycin B Chemical Properties,Usage,Production

Description

Tetromycin B is a cysteine protease inhibitor with Ki values of 0.62, 1.42, 32.5, and 1.59 μM for rhodesain, falcipain-2, cathepsin L, and cathepsin B, respectively. It inhibits the growth of T. brucei in vitro (IC50 = 30.87 μM). Tetromycin B is also cytotoxic to HEK293T kidney cells and J774.1 macrophages (IC50s = 71.77 and 20.2 μM, respectively).

Uses

Tetromycin B is an unusual tetronic acid, structurally related to kijanimicin, chlorothricin, saccharocarcin, tetrocarcin and versipelostatin. Tetromycin B has pronounced activity against antibiotic susceptible and resistant Gram positive bacteria including MRSA. Limited availability has restricted further investigation of this metabolite in the literature. Several members of this class have received considerable literature focus. Versipelostatin inhibits transcription from the promoter of GRP78, a gene that is activated as part of a stress signalling pathway under glucose deprivation resulting in unfolded protein response (UPR). The UPR-inhibitory action is seen only in conditions of glucose deprivation and causes selective and massive killing of the glucose-deprived cells. Tetrocarcin A appears to target the phosphatidylinositide-3'-kinase/Akt signalling pathway.

Uses

Tetromycin B is an unusual tetronic acid structured antibiotic showing efficacy against MRSA.

References

[1] SHEILA M PIMENTEL-ELARDO. New tetromycin derivatives with anti-trypanosomal and protease inhibitory activities.[J]. Marine Drugs, 2011, 9 10: 1682-1697. DOI: 10.3390/md9101682

TetroMycin B Preparation Products And Raw materials

Raw materials

Preparation Products

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180027-84-3, TetroMycin BRelated Search:


  • TetroMycin B
  • 18H-16a,19-Metheno-16aH-benzo[b]naphth[2,1-j]oxacyclotetradecin-18,20(1H)-dione, 2,3,4,4a,6a,9,10,12a,15,16,20a,20b-dodecahydro-4,21-trihydroxy-1,6,7,11,12a,14,15,20a-octamethyl-, (1S,4S,4aS,6aR,7E,11E,12aR,15R,16aS,20aS,20bR)- (9CI)
  • 180027-84-3