製品番号: HY-13024

Rebastinib

Name: Rebastinib
Brand: MedChemExpress
SKU: HY-13024
Price: 77.00 USD
Availability: InStock
Rating: 5 (13 reviews)

(別名: DCC-2036)

13 Cited Publications

カスタマーレビュー

Based on 13 publication(s) in Google Scholar

Rebastinib (DCC-2036) is an orally active, non-ATP-competitive Bcr-Abl inhibitor, with IC₅₀ values of 0.8 nM and 4 nM against Abl1^WT and Abl1^T315I, respectively. Rebastinib potently inhibits CYP2C8 (IC₅₀ = 0.0533 μM) and CYP2C9 (IC₅₀ = 2.54 μM). Rebastinib allosterically inhibits Tie2 with an IC₅₀ of 0.63 nM. Rebastinib inhibits the transcriptional activity of FoxO1. Rebastinib inhibits SRC family kinases, KDR and FLT3 kinases. Rebastinib induces Apoptosis. Rebastinib exerts anti-tumor activity in breast cancer. Rebastinib exerts anti-angiogenic effects. Rebastinib increases myotube diameter and improves reduced contractility. Rebastinib can be used in research related to triple-negative breast cancer, luminal breast cancer, pancreatic neuroendocrine tumors, muscle atrophy, cancer cachexia, chronic myeloid leukemia, and B-lymphocytic leukemia.

商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
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: 99.74%
CAS 番号: 1020172-07-9
分子式: C₃₀H₂₈FN₇O₃
分子量:553.59

保管条件:

Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year

Rebastinib 構造式

CAS 番号: 1020172-07-9

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生物活性
- 製品説明
- IC₅₀ & Target
- Cellular Effect
- 体外実験
- 体内実験
- 臨床実験
化学情報
Publications (13)
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
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生物活性

製品説明

IC₅₀ & Target

CYP2C8

0.0533 μM (IC₅₀)

CYP2C9

2.54 μM (IC₅₀)

Tie2

0.63 nM (IC₅₀)

Abl1^WT

0.8 nM (IC₅₀)

Abl1^T315I

4 nM (IC₅₀)

FOXO1

Bcr-Abl アイソフォーム固有の製品をすべて表示 :

Abl
Bcr-Abl

Cytochrome P450 アイソフォーム固有の製品をすべて表示 :

Tie アイソフォーム固有の製品をすべて表示 :

Tie1
Tie2

FOXO アイソフォーム固有の製品をすべて表示 :

FOXO1
FOXO3

Src 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
BaF3	IC₅₀	120 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 F359C mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 F359C mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	127 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 E255K mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 E255K mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	13 nM Compound: DCC-2036	Antiproliferative activity against mouse BAF3 cells harboring wild type BCR-ABL measured after 72 hrs by MTT assay Antiproliferative activity against mouse BAF3 cells harboring wild type BCR-ABL measured after 72 hrs by MTT assay	[PMID: 35551036]
BaF3	IC₅₀	13 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 T315I mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 T315I mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	14 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 M351T mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 M351T mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	150 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 E255V mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 E255V mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	19 nM Compound: DCC-2036	Antiproliferative activity against mouse BAF3 cells harboring BCR-ABL T315I mutant measured after 72 hrs by MTT assay Antiproliferative activity against mouse BAF3 cells harboring BCR-ABL T315I mutant measured after 72 hrs by MTT assay	[PMID: 35551036]
BaF3	IC₅₀	19 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 T315A mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 T315A mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	24 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 Q252H mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 Q252H mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	3500 nM Compound: DCC-2036	Antiproliferative activity against parent mouse BaF3 cells assessed as inhibition of cell proliferation measured after 72 hrs in presence of IL-3 by MTT assay Antiproliferative activity against parent mouse BaF3 cells assessed as inhibition of cell proliferation measured after 72 hrs in presence of IL-3 by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	36 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 F317L mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 F317L mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	39 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 Y253F mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 Y253F mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	5.4 nM Compound: DCC-2036	Antiproliferative activity against native mouse BaF3 cells assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against native mouse BaF3 cells assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	51 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 L248R mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 L248R mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	56 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 Y253H mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 Y253H mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	6 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 V299L mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 V299L mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	81 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 H396P mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 H396P mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
BaF3	IC₅₀	98 nM Compound: DCC-2036	Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 G250E mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay Antiproliferative activity against mouse BaF3 cells harbouring BCR-ABL1 G250E mutant assessed as inhibition of cell proliferation measured after 72 hrs by MTT assay	[PMID: 21481795]
K562	IC₅₀	5.5 nM Compound: DCC-2036	Antiproliferative activity against human K562 cells measured after 72 hrs by MTT assay Antiproliferative activity against human K562 cells measured after 72 hrs by MTT assay	[PMID: 21481795]

体外実験

Rebastinib (10^-10 M-10^-4 M; 72 h) potently inhibits the proliferation of breast cancer MCF7 and MDA-MB-231 cells. After 72 h of incubation, its IC₅₀ is 2.22 μM against MCF7 cells and 1.63 μM against MDA-MB-231 cells^[1].
Rebastinib (0.5-8.0 μM; 48 h) induces dose-dependent apoptosis in MCF7 and MDA-MB-231 cells after 48 h of incubation; the total apoptosis rate reaches 16.87% in MCF7 cells at a concentration of 8.0 μM, and 21.62% in MDA-MB-231 cells at a concentration of 6.4 μM^[1].
Rebastinib (0.3-30 μM) exerts no significant inhibitory effect on hERG potassium channel currents in HEK 293 cells, with a maximum average inhibition rate of 31.50% at 30 μM^[1].
Rebastinib (5-45 min) potently inhibits CYP2C8 (IC₅₀=0.0533 μM) and CYP2C9 (IC₅₀=2.54 μM), whereas it exhibits only extremely weak inhibition or no inhibition against CYP1A2, CYP2B6, CYP2C19, CYP2D6, and CYP3A4 at concentrations up to 40 μM^[1].
Rebastinib potently inhibits recombinant non-phosphorylated Tie2 kinase, with an IC₅₀ of 0.63 nM and a dissociation half-life as long as 10 h^[2].
Rebastinib (multiple concentrations) inhibits Ang1-induced HUVEC migration with an IC₅₀ of 0.022 nM^[2].
Rebastinib (24 h) potently inhibits the transcriptional activity of FoxO1 in HEK293T cells, with an IC₅₀ of 2.1 × 10^-7 M^[3].
Rebastinib (0.1-3 μM; 24 h) dose-dependently inhibits the Dexamethasone (HY-14648)-induced upregulation of atrophy-related genes (atrogin-1, MuRF-1) and C/EBPβ mRNA, and modulates the mRNA levels of FoxO1/FoxO3 in C2C12 myotubes^[3].
Rebastinib (1 μM; 24 h) reduces atrogin-1 protein levels in C2C12 myotubes without altering the phosphorylation status of FoxO1 or FoxO3^[3].
Rebastinib potently inhibits multiple forms of recombinant ABL1 kinase, including the drug-resistant ABL1^T315I and ABL1^H396P mutants, via a non-ATP-competitive mechanism. It exhibits a prolonged kinase residence time and also inhibits a specific subset of other kinases^[4].

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

Cell Proliferation Assay^[1]

Cell Line:

human breast carcinoma MCF7, MDA-MB-231 cell lines
Concentration:

10^-10 M-10^-4 M
Incubation Time:

72 h
Result:

Inhibited cell proliferation in both cell lines in a concentration-dependent manner, with an IC₅₀ of 2.22 μM for MCF7 cells and 1.63 μM for MDA-MB-231 cells.

Apoptosis Analysis^[1]

Cell Line:

human breast carcinoma MCF7, MDA-MB-231 cell lines
Concentration:

0.5-8.0 μM (MCF7 cells); 0.8-6.4 μM (MDA-MB-231 cells)
Incubation Time:

48 h
Result:

Induced dose-dependent apoptosis in both cell lines.
In MDA-MB-231 cells, total apoptosis increased from 7.95% (control) to 9.8% (0.8 μM), 9.95% (1.6 μM), and 21.62% (6.4 μM), driven primarily by increases in early-stage apoptosis.
In MCF7 cells, total apoptosis increased from 6.88% (control) to 8.2% (0.5 μM), 10.91% (2.0 μM), and 16.87% (8.0 μM), with increases in both early and late-stage apoptosis.

Real Time qPCR^[3]

Cell Line:

mouse C2C12 skeletal muscle myotubes
Concentration:

0.1-3 μM (co-treated with 1 μM DEX)
Incubation Time:

24 h
Result:

Significantly and dose-dependently reduced DEX-induced upregulation of atrogin-1, MuRF-1, and C/EBPβ mRNA.
Decreased basal FoxO1 mRNA levels and the DEX-induced increase in FoxO3 mRNA levels.

Western Blot Analysis^[3]

Cell Line:

mouse C2C12 skeletal muscle myotubes
Concentration:

1 μM (co-treated with 1 μM DEX)
Incubation Time:

24 h
Result:

Significantly reduced DEX-increased atrogin-1 protein levels.
Did not alter levels of total FoxO1, phosphorylated FoxO1, total FoxO3, or phosphorylated FoxO3 compared to DEX-treated vehicle controls.

体内実験

Rebastinib (150 mg/kg; intravenous injection; single dose) produces a statistically significant 44.54% inhibition of MDA-MB-231 triple-negative breast cancer xenograft growth in female SCID mice, with reversible body weight changes^[1].
Rebastinib (150 mg/kg; intravenous injection; single dose) exerts no significant inhibitory effect on the growth of MDA-MB-468 triple-negative breast cancer xenografts in female SCID mice, with only reversible body weight changes observed^[1].
Combination of tosylate salt of Rebastinib (10 mg/kg; p.o.; daily; twice weekly; once weekly) with Eribulin (HY-13442) reduces primary breast tumor growth by 75%, inhibits lung metastasis by 72%, and prolongs survival in mice, while reducing Tie2⁺macrophage infiltration and impairing TMEM-mediated intravasation of tumor cells^[2].
Tosylate of Rebastinib (10 mg/kg; p.o.; once daily; for 4 consecutive weeks) reduces hepatic micrometastases by 75% in PNET models, while decreasing Tie2⁺macrophage infiltration, perfused microvessel density, and promoting vascular maturation, without affecting the growth of primary tumors^[2].
Rebastinib (100 mg/kg; p.o.; once daily) significantly prolongs the survival and reduces the leukemia burden of Balb/c mice with allogeneic transplants of Ba/F3 cells expressing BCR-ABL1^T315I^[4].
Rebastinib (100 mg/kg; p.o.; once daily) significantly prolongs the survival of Balb/c mice with BCR-ABL1^T315I-induced chronic myeloid leukemia-like myeloproliferative neoplasms and reduces their circulating white blood cell counts^[4].
Tosylate of Rebastinib (60 mg/kg; p.o.; twice daily) significantly prolongs the survival of Balb/c mice with BCR-ABL1^T315I-induced B-cell acute lymphoblastic leukemia (B-ALL)^[4].

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

Animal Model:

SCID (female, 5 weeks old, triple-negative breast cancer xenograft via subcutaneous injection of 5×10⁶ MDA-MB-231 cells)^[1]
Dosage:

150 mg/kg
Administration:

i.v.; single dose
Result:

Achieved a statistically significant tumor growth suppressive rate of 44.54% (p<0.05) compared to control.
Caused a maximum 12% body weight loss by day 28, which was recovered by day 38 with a net 6% weight gain.

Animal Model:

SCID (female, 5 weeks old, triple-negative breast cancer xenograft via subcutaneous injection of 5×10⁶ MDA-MB-468 cells)^[1]
Dosage:

150 mg/kg
Administration:

i.v.; single dose
Result:

Showed no significant tumor growth suppression compared to control.
Caused a maximum 8% body weight loss by day 28, which was recovered by day 38 with a net 7.7% weight gain.

Animal Model:

FVB/NJ (female)^[2]
Dosage:

10 mg/kg
Administration:

p.o.; daily; twice weekly; once weekly
Result:

Reduced primary tumor growth by 75% (TGI 75%).
Produced an additive effect with paclitaxel, reducing tumor growth by 90% (TGI 90%).
Reduced lung metastases by 72%; in combination with paclitaxel, reduced lung metastases by 93%.
Extended mouse median survival to at least 196-200 days when combined with eribulin after primary tumor resection, compared with 54 days for eribulin alone and 84 days for vehicle.
Significantly decreased total macrophages and Tie2+ macrophages in tumor tissue and stroma.
Counteracted paclitaxel-induced increases in total macrophages, Tie2+ macrophages, and CD31+ microvessel density, reducing microvessel density to below vehicle levels.
Reduced vascular permeability (extravascular dextran area/CD31 area decreased by ~70%).
Increased vascular ZO-1 staining intensity relative to CD31.
Reduced normalized circulating tumor cells (CTCs/mL blood) by ~75%, impairing TMEM function without altering TMEM density.

Animal Model:

C57Bl6/6J/RIP1-Tag2 (male, 11.5-12.5 weeks old)^[2]
Dosage:

10 mg/kg
Administration:

p.o.; daily; 4 weeks
Result:

Did not detectably inhibit primary pancreatic insulinoma growth, but significantly reduced liver micrometastases by 75% compared with vehicle.
Reduced Tie2 staining in PNET tumors; total macrophage (F4/80+ area) levels were unchanged, but intratumoral Tie2+ macrophages (F4/80+/Tie2+ area percentage) were significantly decreased.
Significantly reduced protumoral Mrc1+/F4/80+ macrophages at the tumor invasive front and decreased the density of perfused (lectin-positive) blood vessels in PNET tumors.
Increased vascular maturation by increasing the proportion of pericyte-covered (Ng2+) blood vessels.

Animal Model:

Balb/c mice (syngeneic recipients)^[4]
Dosage:

100 mg/kg
Administration:

p.o.; once daily
Result:

Achieved circulating plasma levels exceeding 12 μM for up to 24 hours.
Inhibited BCR-ABL1ᵀ³¹⁵ᴵ signaling (phospho-STAT5, phospho-BCR-ABL1) for up to 8 hours in bone marrow and spleen leukemia cells.
Significantly prolonged mouse survival, with survival superior to imatinib at 100 mg/kg twice daily.
Reduced leukemia cell burden in spleens (spleen weight difference was borderline significant, p=0.06).

Animal Model:

Balb/c mice (male donors, sublethally irradiated recipients)^[4]
Dosage:

100 mg/kg
Administration:

p.o.; once daily
Result:

Prolonged median mouse survival from 20 days to 32 days (p=0.007, Wilcoxon test).
Significantly reduced circulating leukocyte counts on day 20 post-transplant (p=0.0002, unpaired t-test).

Animal Model:

Balb/c mice (sublethally irradiated recipients)^[4]
Dosage:

60 mg/kg
Administration:

p.o.; twice daily
Result:

Significantly prolonged median mouse survival to 47 days, with survival superior to vehicle (p=0.0184), imatinib at 100 mg/kg twice daily (p=0.0474), and dasatinib at 10 mg/kg twice daily (p<0.0001, Wilcoxon tests).

臨床実験

NCT Number	Sponsor	Condition	Start Date	Phase A549
NCT01329991	Plexxikon\|		2011-05	PHASE1

化学情報

CAS 番号 1020172-07-9
性状 Solid
分子量 553.59
分子式 C₃₀H₂₈FN₇O₃
Color White to off-white
SMILES

CC(C)(C)C1=NN(C(NC(NC2=C(F)C=C(OC3=CC(C(NC)=O)=NC=C3)C=C2)=O)=C1)C4=CC=C5C(C=CC=N5)=C4
別名

DCC-2036
輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	2 years
	-20°C	1 year

Publications (13)

All Histological Imaging/StainingCell Imaging/Staining

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Journal Impact Factor

Nat Commun

Caveolae-mediated Tie2 signaling contributes to CCM pathogenesis in a brain endothelial cell-specific Pdcd10-deficient mouse model. [Abstract]

2021 Jan 25;12(1):504. PMID: 33495460

Rebastinib purchased from MedChemExpress. Usage Cited in: Nat Commun. 2021 Jan 25;12(1):504. [Abstract]

Rebastinib (1 μM) blunted increased EC sprouting and enlarged lumen formation induced by CCM3 knockdown.

Rebastinib purchased from MedChemExpress. Usage Cited in: Nat Commun. 2021 Jan 25;12(1):504. [Abstract]

Rebastinib (10 μg/g; s.c.; 11 d) diminished the CCM lesions induced by Ccm3 deletion as visualized by whole-brain imaging and H&E staining compared to vehicle treatment in Pdcd10^BECKO mice.

Rebastinib purchased from MedChemExpress. Usage Cited in: Nat Commun. 2021 Jan 25;12(1):504. [Abstract]

Rebastinib (10 μg/g; s.c.; once daily for 11 d) normalized the NG2⁺ pericyte coverage of CD31⁺ microvessels in Pdcd10^BECKO mice.

Rebastinib purchased from MedChemExpress. Usage Cited in: Nat Commun. 2021 Jan 25;12(1):504. [Abstract]

Rebastinib (10 μg/g; s.c.; once daily for 11 d) caussed very fewer CCM lesions in brain of Pdcd10^BECKO mice compared to vehicle group even at age of 2 months.

Rebastinib purchased from MedChemExpress. Usage Cited in: Nat Commun. 2021 Jan 25;12(1):504. [Abstract]

Rebastinib (10 μg/g; s.c.; 11 d) increased pericyte density and diminished pericyte-free caverns in Pdcd10^BECKO mice.
Sci Transl Med

PP2A inhibition is a druggable MEK inhibitor resistance mechanism in KRAS-mutant lung cancer cells. [Abstract]

2018 Jul 18;10(450):eaaq1093. PMID: 30021885
J Clin Invest

Vessels encapsulating tumor clusters promote noninvasive metastasis of hepatocellular carcinoma by shaping an immunosuppressive microenvironment. [Abstract]

2026 Jan 6;136(4):e193758. PMID: 41493808
J Exp Clin Cancer Res

CDK16 promotes the progression and metastasis of triple-negative breast cancer by phosphorylating PRC1. [Abstract]

2022 Apr 21;41(1):149. PMID: 35449080
Brain

Three-dimensional tissue engineered skeletal muscle modelling facioscapulohumeral muscular dystrophy. [Abstract]

2025 May 13;148(5):1723-1739. PMID: 39556762
J Exp Med

TIE2 links MEKK3-KLF2/4 and PI3K signaling in cerebral cavernous malformation. [Abstract]

2026 May 4;223(5):e20251374. PMID: 41891922
J Med Chem

Conformational analysis of the DFG-out kinase motif and biochemical profiling of structurally validated type II inhibitors. [Abstract]

2015 Jan 8;58(1):466-79. PMID: 25478866
J Cell Sci

LRRK2 mutations block NCOA4 trafficking upon iron overload leading to ferroptotic death. [Abstract]

2026 May 28:jcs.264977. PMID: 42206576
Anticancer Drugs

AZD7762 induces CRBN dependent BAG3 degradation through ubiquitin-proteasome pathway. [Abstract]

2024 Jan 1;35(1):46-54. PMID: 37449977
Res Sq

2025 Sep 1.
bioRxiv

2025 August 23.
University of Washington

2025.
Patent

US20170349880A1.

溶剤 & 溶解度

体外:

DMSO : 50 mg/mL (90.32 mM; ultrasonic and warming and heat to 80°C; 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

1.8064 mL

9.0320 mL

18.0639 mL

5 mM

0.3613 mL

1.8064 mL

3.6128 mL

10 mM

0.1806 mL

0.9032 mL

1.8064 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

モル濃度計算機

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

Mass Mass

濃度濃度

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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)

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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 90% (20% SBE-β-CD in Saline)

Solubility: ≥ 2.08 mg/mL (3.76 mM); Clear solution

This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 900 μL 20% SBE-β-CD in Saline, 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
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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:

%
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Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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+
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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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参考文献

[1]. Feng K, et al. The Suppressive Effect of Rebastinib on Triple-negative Breast Cancer Tumors Involves Multiple Mechanisms of Action. Anticancer research. 2023 Jun;43(6):2609-2624. [Content Brief]

[2]. Harney AS, et al. The Selective Tie2 Inhibitor Rebastinib Blocks Recruitment and Function of Tie2 Macrophages in Breast Cancer and Pancreatic Neuroendocrine Tumors. Molecular cancer therapeutics. 2017 Nov;16(11):2486-2501. [Content Brief]

[3]. Sato T, et al. Rebastinib inhibits FoxO1 activity and reduces dexamethasone-induced atrophy and its-related gene expression in cultured myotubes. The journal of physiological sciences : JPS. 2025 Mar;75(1):100012. [Content Brief]

[4]. Chan WW, et al. Conformational control inhibition of the BCR-ABL1 tyrosine kinase, including the gatekeeper T315I mutant, by the switch-control inhibitor DCC-2036. Cancer cell. 2011 Apr 12;19(4):556-68. [Content Brief]

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

Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	1.8064 mL	9.0320 mL	18.0639 mL	45.1598 mL
	5 mM	0.3613 mL	1.8064 mL	3.6128 mL	9.0320 mL
	10 mM	0.1806 mL	0.9032 mL	1.8064 mL	4.5160 mL
	15 mM	0.1204 mL	0.6021 mL	1.2043 mL	3.0107 mL
	20 mM	0.0903 mL	0.4516 mL	0.9032 mL	2.2580 mL
	25 mM	0.0723 mL	0.3613 mL	0.7226 mL	1.8064 mL
	30 mM	0.0602 mL	0.3011 mL	0.6021 mL	1.5053 mL
	40 mM	0.0452 mL	0.2258 mL	0.4516 mL	1.1290 mL
	50 mM	0.0361 mL	0.1806 mL	0.3613 mL	0.9032 mL
	60 mM	0.0301 mL	0.1505 mL	0.3011 mL	0.7527 mL
	80 mM	0.0226 mL	0.1129 mL	0.2258 mL	0.5645 mL

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Rebastinib

13 Cited Publications

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Rebastinib

Nilotinib

Olverembatinib

Ponatinib

Bafetinib

Quizartinib

Bemcentinib

Imatinib

Asciminib

Radotinib

Dasatinib

Altiratinib

Doramapimod

MedChemExpress（MCE）の使用を引用している文献 Rebastinib

Bcr-Abl アイソフォーム固有の製品をすべて表示

Cytochrome P450 アイソフォーム固有の製品をすべて表示

Tie アイソフォーム固有の製品をすべて表示

FOXO アイソフォーム固有の製品をすべて表示

Src 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

Publications (13)

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

Rebastinib

Nilotinib

Olverembatinib

Ponatinib

Bafetinib

Quizartinib

Bemcentinib

Imatinib

Asciminib

Radotinib

Dasatinib

Altiratinib

Doramapimod

MedChemExpress（MCE）の使用を引用している文献 Rebastinib

Bcr-Abl アイソフォーム固有の製品をすべて表示

Cytochrome P450 アイソフォーム固有の製品をすべて表示

Tie アイソフォーム固有の製品をすべて表示

FOXO アイソフォーム固有の製品をすべて表示

Src 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

Publications (13)

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

Rebastinib 関連分類

HY-13024 関連分類

Bioz