製品番号: HY-112609

QCA570

Name: QCA570
Brand: MedChemExpress
SKU: HY-112609
Price: 390.00 USD
Availability: InStock
Rating: 5 (1 reviews)

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Based on 1 Customer Validation

QCA570 is a pan-BET-BRD PROTAC degrader. QCA570 degrades BRD2/3/4 and BRDT via cereblon and the ubiquitin-proteasome pathway, inhibits the expression of c-MYC, EZH2 and Mcl-1, induces tumor cell apoptosis, cycle arrest and regression, and exerts a synergistic inhibitory effect on Osimertinib (HY-15772)-resistant EGFR-mutant non-small cell lung cancer. QCA570 can be used in the research of acute myeloid leukemia, acute lymphoblastic leukemia, bladder cancer and non-small cell lung cancer.
(Pink: BET ligand (HY-44103); Blue: Cereblon ligand (HY-131318); Black: linker (HY-W035972)).

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研究用途以外に使用した場合、当社は一切の責任を負いかねます。

純度: 99.30%
CAS 番号: 2207569-08-0
分子式: C₃₉H₃₃N₇O₄S
分子量:695.79

保管条件:

-20°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

QCA570 構造式

CAS 番号: 2207569-08-0

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数量

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生物活性
- 製品説明
- IC₅₀ & Target
- Cellular Effect
- 体外実験
- 体内実験
化学情報
溶剤 & 溶解度
- 体外
- 体内
純度とドキュメンテーション
参考文献
Help & FAQs
関連分類
Bioz

生物活性

製品説明

QCA570 is a pan-BET-BRD PROTAC degrader. QCA570 degrades BRD2/3/4 and BRDT via cereblon and the ubiquitin-proteasome pathway, inhibits the expression of c-MYC, EZH2 and Mcl-1, induces tumor cell apoptosis, cycle arrest and regression, and exerts a synergistic inhibitory effect on Osimertinib (HY-15772)-resistant EGFR-mutant non-small cell lung cancer. QCA570 can be used in the research of acute myeloid leukemia, acute lymphoblastic leukemia, bladder cancer and non-small cell lung cancer^[1]^[2]^[3]^[4]^[5]^[6]. (Pink: BET ligand (HY-44103); Blue: Cereblon ligand (HY-131318); Black: linker (HY-W035972)).

IC₅₀ & Target^[5]^[3]^[2]

BRD2

BRD3

BRD4

Mcl-1

EZH2

PROTACs アイソフォーム固有の製品をすべて表示 :

Epigenetic Reader Domain アイソフォーム固有の製品をすべて表示 :

Histone Methyltransferase アイソフォーム固有の製品をすべて表示 :

Bcl-2 Family アイソフォーム固有の製品をすべて表示 :

Cellular Effect

Cell Line	Type	Value	Description	References
RS4-11	IC₅₀	50 pM	Cell growth inhibition against RS4;11 leukemia cells. Cell growth inhibition against RS4;11 leukemia cells.	30019901
Leukemia cell	IC₅₀	120 pM	Induction of cell death/apoptosis in CD34-enriched leukemia stem cells from primary AML samples measured by flow cytometry for DAPI-Annexin V binding after 3 days of incubation. Induction of cell death/apoptosis in CD34-enriched leukemia stem cells from primary AML samples measured by flow cytometry for DAPI-Annexin V binding after 3 days of incubation.	30019901
MV4-11	IC₅₀	8.3 pM	Cell growth inhibition against human acute leukemia MV4;11 cells assessed via lactate dehydrogenase-based WST-8 assay after 4 days of incubation. Cell growth inhibition against human acute leukemia MV4;11 cells assessed via lactate dehydrogenase-based WST-8 assay after 4 days of incubation.	36733715
MOLM-13	IC₅₀	62 pM	Cell growth inhibition against human acute leukemia MOLM-13 cells assessed via lactate dehydrogenase-based WST-8 assay after 4 days of incubation. Cell growth inhibition against human acute leukemia MOLM-13 cells assessed via lactate dehydrogenase-based WST-8 assay after 4 days of incubation.	36733715
RS4-11	IC₅₀	32 pM	Cell growth inhibition against human acute leukemia RS4;11 cells assessed via lactate dehydrogenase-based WST-8 assay after 4 days of incubation. Cell growth inhibition against human acute leukemia RS4;11 cells assessed via lactate dehydrogenase-based WST-8 assay after 4 days of incubation.	36733715
5637	DC₅₀	1.184 nM	Half-maximal degradation of BRD4 protein in human 5637 bladder cancer cells after 9 h incubation measured via Western blot analysis. Half-maximal degradation of BRD4 protein in human 5637 bladder cancer cells after 9 h incubation measured via Western blot analysis.	35261801
J82	DC₅₀	0.4507 nM	Half-maximal degradation of BRD4 protein in human J82 bladder cancer cells after 9 h incubation measured via Western blot analysis. Half-maximal degradation of BRD4 protein in human J82 bladder cancer cells after 9 h incubation measured via Western blot analysis.	35261801
T-24	DC₅₀	0.2313 nM	Half-maximal degradation of BRD4 protein in human T24 bladder cancer cells after 9 h incubation measured via Western blot analysis. Half-maximal degradation of BRD4 protein in human T24 bladder cancer cells after 9 h incubation measured via Western blot analysis.	35261801
UMUC3	DC₅₀	1.589 nM	Half-maximal degradation of BRD4 protein in human UM-UC-3 bladder cancer cells after 9 h incubation measured via Western blot analysis. Half-maximal degradation of BRD4 protein in human UM-UC-3 bladder cancer cells after 9 h incubation measured via Western blot analysis.	35261801
EJ	DC₅₀	1.041 nM	Half-maximal degradation of BRD4 protein in human EJ-1 bladder cancer cells after 9 h incubation measured via Western blot analysis. Half-maximal degradation of BRD4 protein in human EJ-1 bladder cancer cells after 9 h incubation measured via Western blot analysis.	35261801
5637	IC₅₀	2.68 nM	Half-maximal inhibition of cell viability in human 5637 bladder cancer cells after 72 h incubation measured via CCK-8 assay. Half-maximal inhibition of cell viability in human 5637 bladder cancer cells after 72 h incubation measured via CCK-8 assay.	35261801
J82	IC₅₀	10.81 nM	Half-maximal inhibition of cell viability in human J82 bladder cancer cells after 72 h incubation measured via CCK-8 assay. Half-maximal inhibition of cell viability in human J82 bladder cancer cells after 72 h incubation measured via CCK-8 assay.	35261801
T-24	IC₅₀	30.44 nM	Half-maximal inhibition of cell viability in human T24 bladder cancer cells after 72 h incubation measured via CCK-8 assay. Half-maximal inhibition of cell viability in human T24 bladder cancer cells after 72 h incubation measured via CCK-8 assay.	35261801
UMUC3	IC₅₀	21.96 nM	Half-maximal inhibition of cell viability in human UM-UC-3 bladder cancer cells after 72 h incubation measured via CCK-8 assay. Half-maximal inhibition of cell viability in human UM-UC-3 bladder cancer cells after 72 h incubation measured via CCK-8 assay.	35261801
EJ	IC₅₀	15.59 nM	Half-maximal inhibition of cell viability in human EJ-1 bladder cancer cells after 72 h incubation measured via CCK-8 assay. Half-maximal inhibition of cell viability in human EJ-1 bladder cancer cells after 72 h incubation measured via CCK-8 assay.	35261801
H1975	IC₅₀	0.3 nM	Cell survival inhibition against human NSCLC H1975 cells assessed by SRB assay following 3-day incubation. Cell survival inhibition against human NSCLC H1975 cells assessed by SRB assay following 3-day incubation.	blood-2019-131759
NCI-H157	IC₅₀	0.3 nM	Cell survival inhibition against human NSCLC H157 cells assessed by SRB assay following 3-day incubation. Cell survival inhibition against human NSCLC H157 cells assessed by SRB assay following 3-day incubation.	blood-2019-131759
Calu-1	IC₅₀	0.3 nM	Cell survival inhibition against human NSCLC Calu-1 cells assessed by SRB assay following 3-day incubation. Cell survival inhibition against human NSCLC Calu-1 cells assessed by SRB assay following 3-day incubation.	blood-2019-131759
NCI-H1299	IC₅₀	100 nM	Cell survival inhibition against human NSCLC H1299 cells assessed by SRB assay following 3-day incubation. Cell survival inhibition against human NSCLC H1299 cells assessed by SRB assay following 3-day incubation.	blood-2019-131759
EKVX	IC₅₀	100 nM	Cell survival inhibition against human NSCLC EKVX cells assessed by SRB assay following 3-day incubation. Cell survival inhibition against human NSCLC EKVX cells assessed by SRB assay following 3-day incubation.	blood-2019-131759
MV4-11	IC₅₀	0.0083 nM	Antiproliferative activity against human MV4;11 cells assessed as inhibition of cell proliferation. Antiproliferative activity against human MV4;11 cells assessed as inhibition of cell proliferation.	34494353

体外実験

QCA570 (compound 35) (for 4 days) potently inhibits the growth of MV4;11, MOLM-13 and RS4;11 human acute leukemia cells, with IC₅₀ values of 8.3 pM, 62 pM and 32 pM, respectively^[1].
QCA570 (30 pM) degrades all BET-BRD proteins in RS4;11 leukemia cells and inhibits the growth of RS4;11 cells with an IC₅₀ of 50 pM^[4].
QCA570 (4 h) degrades BRD4 and inhibits c-MYC in CD34-enriched leukemic stem cells from primary AML samples^[4].
QCA570 (0.01-10 nM; 3 h) potently induces the degradation of BRD2, BRD3 and BRD4 proteins at picomolar concentrations and suppresses c-Myc protein levels in MV4;11 and RS4;11 human acute leukemia cells after 3 hours of incubation^[1].
QCA570 (0.5 nM; 3 h) induces the degradation of BRD2, BRD3 and BRD4 proteins in RS4;11 human acute leukemia cells via cereblon-dependent, neddylation-dependent and proteasome-dependent mechanisms, with no effect on GSPT1 protein levels^[1].
QCA570 (0.01-100 nM; 9 h) potently induces proteasome-dependent degradation of BRD2, BRD3 and BRD4 proteins in 5637, J82, T24, UM-UC-3 and EJ-1 human bladder cancer cells^[2].
QCA570 (10-100 nM) inhibits the expression of BRD4 target genes c-MYC and EZH2 at both mRNA and protein levels in human bladder cancer J82, T24 and 5637 cells^[2].
QCA570 (72 h) potently inhibits the proliferation of 5637, J82, T24, UM-UC-3 and EJ-1 human bladder cancer cells, with IC₅₀ values ranging from 2.68 to 30.44 nM^[2].
QCA570 potently reduces the viability of human non-small cell lung cancer cell lines (H1975, H157, Calu-1, H1299, H1650, H460, H1792, PC-9, EKVX, H1944), with IC₅₀ values ranging from 0.3 nM to 100 nM, and its sensitivity correlates with higher baseline BET protein levels^[3].
QCA570 potently inhibits the proliferation of MV4;11 cells, with an IC₅₀ of 0.0083 nM^[5].
QCA570 exhibits no toxicity to normal CD34-positive hematopoietic cells in apoptosis assays and colony formation assays^[4].
QCA570 (0.01-10 nM; 24-48 h) potently induces apoptosis in human acute leukemia cell lines MV4;11, MOLM-13 and RS4;11 in a dose- and time-dependent manner, with faster apoptotic kinetics observed in MV4;11 and MOLM-13 cells than in RS4;11 cells^[1].
QCA570 (0.1-0.3 nM; 24 h) induces PARP cleavage in human acute leukemia cells MV4;11 and RS4;11 at picomolar concentrations. After 24 h of treatment, caspase 3 activation is detectable in MV4;11 cells, but this phenomenon is not observed in RS4;11 cells at the same time point^[1].
QCA570 (10-100 nM; 72 h) induces dose-dependent apoptosis in 5637, J82, T24, UM-UC-3 and EJ-1 human bladder cancer cells, as detected by Annexin V-FITC/PI staining, activated caspase-3 expression assay and TUNEL staining^[2].
QCA570 (5-10 nM; 24 h) induces apoptosis in human non-small cell lung cancer cell lines (H157, H1975, H1650, Calu-1), where downregulation of Mcl-1 plays a key mediating role, while Bim is dispensable for this activity^[3].
QCA570 (1-10 nM; 7 h) potently and rapidly reduces the levels of BRD4, BRD3, BRD2, Mcl-1 and Bim in human non-small cell lung cancer cell lines (H157, H1975, Calu-1) at concentrations as low as 1 nM, and exerts cell-specific effects on c-Myc levels^[3].
QCA570 (0.3125-30 nM; 3 days, 36-72 h, every 3 days for 12 days) acts synergistically with Osimertinib (HY-15772) to reduce cell viability, induce apoptosis, and inhibit colony formation in Osimertinib-resistant human EGFR-mutant non-small cell lung cancer cell lines (PC-9/AR, PC-9/GR/AR, HCC827/AR)^[3].
Combination treatment with QCA570 (1 nM; 12 h) and Osimertinib exerts a synergistic apoptosis-inducing effect in Osimertinib-resistant human EGFR-mutant non-small cell lung cancer cell lines (PC-9/AR, PC-9/GR/AR, HCC827/AR), and this effect is mainly mediated by enhanced Mcl-1 degradation^[3].
QCA570 (10 nM; 72 h) induces G₂/M phase cell cycle arrest in human bladder cancer 5637 cells^[2].
QCA570 (100 nM; 8-48 h) inhibits the migration of human bladder cancer cell lines 5637, EJ-1, J82 and T24^[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis^[1]

Cell Line:

MV4;11, RS4;11
Concentration:

0.01, 0.03, 0.1, 0.3, 1, 3, 10 nM
Incubation Time:

3 h
Result:

Reduced levels of BRD3 and BRD4 proteins at 10 pM in RS4;11 cells after 3 h.
Reduced BRD2 levels at 30-100 pM in RS4;11 cells after 3 h.
Reduced BRD3 and BRD4 levels at 10 pM in MV4;11 cells after 3 h.
Reduced BRD2 levels at 30 pM in MV4;11 cells after 3 h.
Reduced c-Myc protein levels at 10 pM in RS4;11 cells after 3 h.
Reduced c-Myc protein levels at 30 pM in MV4;11 cells after 3 h.
Induced complete degradation of BRD2, BRD3, and BRD4 at 0.5 nM in RS4;11 cells after 3 h.

Western Blot Analysis^[1]

Cell Line:

RS4;11
Concentration:

0.5 nM
Incubation Time:

3 h
Result:

Degradation of BRD2, BRD3, and BRD4 proteins was completely blocked by pre-treatment with cereblon modulator, NEDD8-activating enzyme inhibitor, proteasome inhibitor (peptidyl aldehyde), or proteasome inhibitor (epoxyketone).
Had no effect on GSPT1 protein levels in either MV4;11 or RS4;11 cells.

Apoptosis Analysis^[1]

Cell Line:

MV4;11, MOLM-13, RS4;11
Concentration:

0.01, 0.03, 0.1, 0.3, 1, 3, 10 nM
Incubation Time:

24, 48 h
Result:

Induced > 60% apoptosis at 1 nM in MV4;11 and MOLM-13 cells after 24 h.
Induced minimal apoptosis at 0.1 nM in RS4;11 cells after 24 h.
Induced 15-30% apoptosis at 0.3-10 nM in RS4;11 cells after 24 h.
Induced > 40% apoptosis at 0.1 nM in RS4;11 cells after 48 h.

Western Blot Analysis^[1]

Cell Line:

MV4;11, RS4;11
Concentration:

0.01, 0.03, 0.1, 0.3, 1, 3, 10 nM
Incubation Time:

24 h
Result:

Induced robust cleavage of PARP at 0.1-0.3 nM in both MV4;11 and RS4;11 cells after 24 h.
Induced caspase 3 activation at 0.3 nM in MV4;11 cells after 24 h.
No caspase 3 cleavage was detected in RS4;11 cells after 24 h.

Western Blot Analysis^[2]

Cell Line:

5637, J82, T24, UM-UC-3, EJ-1
Concentration:

0.01, 0.1, 1, 10, 100, 1000 nM (9 h incubation); 30 nM (1-24 h incubation)
Incubation Time:

9 h (0.01-100 nM); 1, 2, 3, 6, 9, 12, 24 h (30 nM)
Result:

Induced dose-dependent degradation of BRD2, BRD3, and BRD4 proteins across all five bladder cancer cell lines after 9 h of incubation.
Largely depleted BRD4 at 3 nM in each cell line, with BRD4 degradation half-maximal (DC₅₀) values of 1.184 nM (5637), 0.4507 nM (J82), 0.2313 nM (T24), 1.589 nM (UM-UC-3), and 1.041 nM (EJ-1).
Peaked BRD4 degradation within 1 h in 5637, T24, and UM-UC-3 cells, and within 3 h in J82 and EJ-1 cells at 30 nM, with time-dependent degradation also observed for BRD2 and BRD3.

Cell Cycle Analysis^[2]

Cell Line:

5637
Concentration:

10 nM
Incubation Time:

72 h
Result:

Induced G2/M phase arrest in 5637 cells, resulting in a decrease in the percentage of cells in G1 phase and an increase in the percentage of cells in G2/M phase compared to vehicle control.

Cell Migration Assay ^[2]

Cell Line:

5637, EJ-1, J82, T24
Concentration:

100 nM
Incubation Time:

8, 24, 48 h
Result:

Significantly suppressed the migration of 5637, EJ-1, J82, and T24 cells, as evidenced by reduced wound closure compared to vehicle control after 24 h (5637, EJ-1, T24) or 48 h (J82) of incubation.

Apoptosis Analysis^[2]

Cell Line:

5637, J82, T24, UM-UC-3, EJ-1
Concentration:

10, 100 nM (flow cytometry); 0.001, 0.01, 0.1 μM (Western blot)
Incubation Time:

72 h
Result:

Induced dose-dependent cell apoptosis across all five bladder cancer cell lines, with more than 50% of cells undergoing apoptosis in J82 and 5637 lines at the higher concentration.
Increased levels of cleaved caspase-3 (a marker of apoptosis) in 5637, J82, and T24 cells incubated with QCA570.
Confirmed increased apoptotic cells in QCA570-incubated 5637, J82, and T24 cells compared to vehicle control via TUNEL staining.

Apoptosis Analysis^[3]

Cell Line:

Human NSCLC cell lines (H157, H1975, H1650, Calu-1)
Concentration:

5, 10 nM
Incubation Time:

24 h (flow cytometry); 22 h (Western blot)
Result:

Increased the annexin V-positive cell population in all tested cell lines.
Induced cleavage of PARP, caspase-8, and caspase-3, confirming apoptosis induction.
Had its apoptosis-inducing effect blocked by enforced ectopic expression of Mcl-1 in H157 and H1975 cells.
Showed no change in apoptosis induction in H157 and H1975 cells with Bim knockout.

Western Blot Analysis^[3]

Cell Line:

Human NSCLC cell lines (H157, H1975, Calu-1)
Concentration:

1 nM, 2.5 nM, 5 nM, 10 nM (7 h incubation); 10 nM (time-course incubation)
Incubation Time:

7 h; 3, 6, 9, 12, 15 h
Result:

Decreased the levels of BRD4, BRD3, and BRD2 potently and rapidly, with reduction detectable as early as 3 h post-treatment and achievable at 1 nM.
Decreased levels of Mcl-1 and Bim with similar potency, rapidness, and durability.
Decreased c-Myc levels quickly and sustainably in H157 cells, caused transient reduction in H1975 cells, and showed no reduction in Calu-1 cells.
Downregulated Mcl-1 mRNA but not Bim mRNA in H157 cells.

Western Blot Analysis^[3]

Cell Line:

Osimertinib-resistant human EGFR-mutant NSCLC cell lines (PC-9/AR, PC-9/GR/AR, HCC827/AR)
Concentration:

1 nM
Incubation Time:

12 h
Result:

Decreased Mcl-1 and c-Myc levels more effectively in combination with Osimertinib than either single agent in all three tested cell lines.
Did not enhance Bim elevation in combination with Osimertinib, and alone decreased Bim levels in HCC827/AR cells.
Had its enhanced apoptosis-inducing and mitochondrial Cyt C/Smac release effects abrogated by enforced ectopic Mcl-1 expression in HCC827/AR cells.

体内実験

QCA570 (compound 35) (1-5 mg/kg; i.v.; single dose, three times per week for 3 weeks) achieves complete and durable tumor regression at well-tolerated doses of 1, 2.5 and 5 mg/kg administered three times per week for 3 weeks in the RS4;11 acute leukemia xenograft model in SCID mice, and a single dose as low as 1 mg/kg induces significant degradation of BET proteins and c-Myc in tumor tissues^[1].
QCA570 (1-5 mg/kg; intravenous injection; three times per week for 2 weeks) achieves complete and durable tumor regression at the well-tolerated dose of 5 mg/kg administered three times per week for 2 weeks, and also achieves complete tumor regression at 1 mg/kg under the same dosing regimen, in MV4;11 acute leukemia xenograft models in SCID mice^[1].
QCA570 (0.5 mg/kg; i.p.; twice weekly) alone shows limited efficacy against Osimertinib-resistant EGFR-mutant non-small cell lung cancer xenografts, but when combined with Osimertinib, it significantly enhances tumor growth inhibition with good tolerance^[3].
QCA570 completely abrogates tumor growth in a mouse xenograft model of human acute leukemia^[6].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:

SCID mice (acute leukemia xenograft model, tumors grown to ~100 mm³)^[1]
Dosage:

1, 2.5, 5 mg/kg
Administration:

i.v.; single dose; 3 times per week for 3 weeks; weekly
Result:

Dramatically reduced BRD2, BRD3, BRD4, and c-Myc protein levels in tumor tissue at 1 h, 6 h, and 24 h post-treatment.
Achieved more effective reduction of BRD4 levels at 24 h with 5 mg/kg single dose.
Induced robust PARP cleavage (apoptosis) at 6 h and 24 h with 1 mg/kg and 5 mg/kg single doses.
Achieved complete and long-lasting tumor regression with 1, 2.5, and 5 mg/kg doses administered 3 times per week for 3 weeks.
Achieved complete tumor growth inhibition but not regression with 5 mg/kg weekly dose.
Caused minimal animal weight loss across all treatment groups.

Animal Model:

SCID mice (acute leukemia xenograft model, tumors grown to ~100 mm³)^[1]
Dosage:

1, 5 mg/kg
Administration:

i.v.; 3 times per week for 2 weeks
Result:

Achieved complete tumor regression with 1 mg/kg dose administered 3 times per week for 2 weeks.
Achieved complete and long-lasting tumor regression with 5 mg/kg dose administered 3 times per week for 2 weeks.
Caused a maximum weight loss of less than 10%.

Animal Model:

NU(NCr)-Foxn1nu (4-week-old female, flank injection of 2×10⁶ HCC827/AR osimertinib-resistant EGFR-mutant NSCLC cells)^[3]
Dosage:

0.5 mg/kg
Administration:

i.p.; twice per week
Result:

Exerted limited effects on suppressing HCC827/AR xenograft growth.
Significantly inhibited tumor growth when combined with Osimertinib compared to either single agent.
Caused limited body weight reduction.

化学情報

CAS 番号 2207569-08-0
性状 Solid
分子量 695.79
分子式 C₃₉H₃₃N₇O₄S
Color White to off-white
SMILES

O=C(N(C1CCC(NC1=O)=O)C2)C3=C2C(C#CCCCN4N=CC(C#CC(S5)=C(CC6=CC=CC=C6)C(COC7)=C5N8C7=NN=C8C)=C4)=CC=C3
輸送条件

Room temperature in continental US; may vary elsewhere.
保管条件

-20°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶剤 & 溶解度

体外:

DMSO : 40 mg/mL (57.49 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

1.4372 mL

7.1861 mL

14.3722 mL

5 mM

0.2874 mL

1.4372 mL

2.8744 mL

10 mM

0.1437 mL

0.7186 mL

1.4372 mL

Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.

Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

モル濃度計算機

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

濃度濃度

体積体積

分子量分子量

希釈計算機

濃度 _(開始) × 体積 _(開始) = 濃度 _(終了) × 体積 _(終了)

濃度 _(開始) 濃度 _(開始)

体積 _(開始) 体積 _(開始)

濃度 _(終了) 濃度 _(終了)

体積 _(終了) 体積 _(終了)

体内:

Select the appropriate dissolution method based on your experimental animal and administration route.

Stock Solution Working Solution

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline

Solubility: 2 mg/mL (2.87 mM); Suspended solution; Need ultrasonic

This protocol yields a suspended solution of 2 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

Protocol 2

Add each solvent one by one: 10% DMSO 90% Corn Oil

Solubility: ≥ 2 mg/mL (2.87 mM); Clear solution

This protocol yields a clear solution of ≥ 2 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.0 mg/mL) to 900 μL Corn oil, and mix evenly.

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

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mg/kg
Animal Weight (Per Animal) Animal Weight (Per Animal)
g
Dosing Volume (Per Animal) Dosing Volume (Per Animal)
μL
Number of Animals Number of Animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Please enter your animal formula composition:

%
DMSO +

Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).

Working solution concentration: 0.22 mg/mL

純度とドキュメンテーション

バッチを選択:

純度: 99.98%

Assay: 99.98%

ee.: 99.98%

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CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
取扱説明書 (2659 KB)

参考文献

[1]. Qin C, et al. Discovery of QCA570 as an Exceptionally Potent and Efficacious Proteolysis Targeting Chimera (PROTAC) Degrader of the Bromodomain and Extra-Terminal (BET) Proteins Capable of Inducing Complete and Durable Tumor Regression. Journal of medicinal chemistry. 2018 Aug 09;61(15):6685-6704. [Content Brief]

[2]. Wang Q, et al. Lethal activity of BRD4 PROTAC degrader QCA570 against bladder cancer cells. Frontiers in chemistry. 2023;11:1121724.

[3]. Liu C, et al. The novel BET degrader, QCA570, is highly active against the growth of human NSCLC cells and synergizes with osimertinib in suppressing osimertinib-resistant EGFR-mutant NSCLC cells. American journal of cancer research. 2022;12(2):779-792. [Content Brief]

[4]. Malathi Kandarp, et al. Superior Pre-Clinical Efficacy of Novel Protac Based BET Degrader in a Large Acute Myeloid Leukemia Cohort, Blood, Volume 134, Supplement 1, 2019, Page 3936, ISSN 0006-4971.

[5]. Hu Z, et al. Recent Developments in PROTAC-Mediated Protein Degradation: From Bench to Clinic. Chembiochem : a European journal of chemical biology. 2022 Jan 19;23(2):e202100270. [Content Brief]

[6]. Zou Y, et al. The PROTAC technology in drug development. Cell biochemistry and function. 2019 Jan;37(1):21-30.

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	1.4372 mL	7.1861 mL	14.3722 mL	35.9304 mL
	5 mM	0.2874 mL	1.4372 mL	2.8744 mL	7.1861 mL
	10 mM	0.1437 mL	0.7186 mL	1.4372 mL	3.5930 mL
	15 mM	0.0958 mL	0.4791 mL	0.9581 mL	2.3954 mL
	20 mM	0.0719 mL	0.3593 mL	0.7186 mL	1.7965 mL
	25 mM	0.0575 mL	0.2874 mL	0.5749 mL	1.4372 mL
	30 mM	0.0479 mL	0.2395 mL	0.4791 mL	1.1977 mL
	40 mM	0.0359 mL	0.1797 mL	0.3593 mL	0.8983 mL
	50 mM	0.0287 mL	0.1437 mL	0.2874 mL	0.7186 mL

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QCA570

BETd-260

GNE-987

ARV-771

PROTAC BET degrader-2

MZP-54

ARV-825

MZ 1

ACBI1

dBET1

dTRIM24

VZ185

A1874

PROTACs アイソフォーム固有の製品をすべて表示

Epigenetic Reader Domain アイソフォーム固有の製品をすべて表示

Histone Methyltransferase アイソフォーム固有の製品をすべて表示

Bcl-2 Family アイソフォーム固有の製品をすべて表示

生物活性

化学情報

溶剤 & 溶解度

純度とドキュメンテーション

参考文献

Help & FAQs

Complete Stock Solution Preparation Table

Bioz

QCA570

BETd-260

GNE-987

ARV-771

PROTAC BET degrader-2

MZP-54

ARV-825

MZ 1

ACBI1

dBET1

dTRIM24

VZ185

A1874

PROTACs アイソフォーム固有の製品をすべて表示

Epigenetic Reader Domain アイソフォーム固有の製品をすべて表示

Histone Methyltransferase アイソフォーム固有の製品をすべて表示

Bcl-2 Family アイソフォーム固有の製品をすべて表示

生物活性

化学情報

溶剤 & 溶解度

純度とドキュメンテーション

参考文献

Help & FAQs

Complete Stock Solution Preparation Table

QCA570 関連分類

HY-112609 関連分類

Bioz