MedKoo Cat#: 130594 | Name: TBE56

Description:

WARNING: This product is for research use only, not for human or veterinary use.

TBE56 is actually a potent and selective BACH1 degrader. BACH1 (BTB and CNC Homology 1) is a transcriptional repressor implicated in cancer metastasis and oxidative stress response. TBE56 promotes proteasomal degradation of BACH1, leading to upregulation of its target genes like HMOX1 (heme oxygenase 1). In cellular studies, TBE56 induces robust BACH1 degradation in human cancer cell lines (e.g., MDA-MB-231) with a DC₅₀ (degradation concentration 50%) in the low nanomolar range (~20–50 nM) and significantly increases HMOX1 mRNA levels by more than 10-fold within 6 hours. In xenograft models, TBE56 reduces BACH1 protein levels in tumors and suppresses lung metastasis without notable toxicity.

Chemical Structure

TBE56
TBE56
CAS#1459836-79-3

Theoretical Analysis

MedKoo Cat#: 130594

Name: TBE56

CAS#: 1459836-79-3

Chemical Formula: C37H43N5O6S

Exact Mass: 685.2934

Molecular Weight: 685.84

Elemental Analysis: C, 64.80; H, 6.32; N, 10.21; O, 14.00; S, 4.67

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
TBE 56, TBE-56; TBE56;
IUPAC/Chemical Name
Hexanoic acid, 6-[[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]amino]-, [(1S,4aR,8aR,10aS)-3,7-dicyano-8a-ethynyl-1,2,4a,6,8a,9,10,10a-octahydro-1,4a-dimethyl-2,6-dioxo-1-phenanthrenyl]methyl ester
InChi Key
TZPQJPJUXPUYDR-GSQIMELKSA-N
InChi Code
InChI=1S/C37H43N5O6S/c1-4-37-14-13-28-35(2,29(37)16-26(43)23(18-37)19-38)17-24(20-39)33(46)36(28,3)22-48-31(45)12-6-5-9-15-40-30(44)11-8-7-10-27-32-25(21-49-27)41-34(47)42-32/h1,16-18,25,27-28,32H,5-15,21-22H2,2-3H3,(H,40,44)(H2,41,42,47)/t25-,27-,28-,32-,35+,36+,37+/m0/s1
SMILES Code
C#C[C@@]12C([C@]3([C@]([C@](C)(C(C(C#N)=C3)=O)COC(CCCCCNC(CCCC[C@H]4[C@]5([H])[C@](NC(N5)=O)([H])CS4)=O)=O)([H])CC1)C)=CC(C(C#N)=C2)=O
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 685.84 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1. Moreno R, Casares L, Higgins M, Ali KX, Honda T, Wiel C, Sayin VI, Dinkova-Kostova AT, de la Vega L. Biotinylation of an acetylenic tricyclic bis(cyanoenone) lowers its potency as an NRF2 activator while creating a novel activity against BACH1. Free Radic Biol Med. 2022 Oct;191:203-211. doi: 10.1016/j.freeradbiomed.2022.08.041. Epub 2022 Sep 6. PMID: 36084789.