CC-885

Name: CC-885
Brand: MedChemExpress
SKU: HY-101488
Rating: 5.0 (12 reviews)

Cat. No.: HY-101488 Purity: 99.85%: FAQs
Data Sheet SDS COA Handling Instructions

Molarity Calculator

CC-885 is a cereblon (CRBN) modulator with potent anti-tumour activity. CC-885 is also a known degrader of GSPT1, inhibiting protein translation.

For research use only. We do not sell to patients.

CC-885 Chemical Structure

CAS No. : 1010100-07-8

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Free Sample (0.1 - 0.5 mg)		Apply Now
5 mg	USD 150	In-stock	Estimated Time of Arrival: December 31
10 mg	USD 210	In-stock	Estimated Time of Arrival: December 31
25 mg	USD 390	In-stock	Estimated Time of Arrival: December 31
50 mg	USD 630	In-stock	Estimated Time of Arrival: December 31
100 mg	USD 1000	In-stock	Estimated Time of Arrival: December 31
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Customer Review

Based on 12 publication(s) in Google Scholar

12 Publications Citing Use of MCE CC-885

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von Hippel-Lindau (VHL) MDM2 Cereblon IAP

Biological Activity
Protocol
Purity & Documentation
References
Customer Review

Description

CC-885 is a cereblon (CRBN) modulator with potent anti-tumour activity. CC-885 is also a known degrader of GSPT1, inhibiting protein translation.

IC₅₀ & Target

CRBN^[1].

Cellular Effect

Cell Line	Type	Value	Description	References
HL-60	IC₅₀	0.003 μM Compound: 3; CC-885	Antiproliferative activity against human HL-60 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay Antiproliferative activity against human HL-60 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
JeKo-1	IC₅₀	1.2 nM Compound: CC-885	Antiproliferative activity against human JeKo1 cells measured after 72 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay Antiproliferative activity against human JeKo1 cells measured after 72 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay	[PMID: 31125896]
Kasumi 1	IC₅₀	0.01 μM Compound: 3; CC-885	Antiproliferative activity against human Kasumi 1 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay Antiproliferative activity against human Kasumi 1 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
Kasumi 1	IC₅₀	0.8 nM Compound: CC-885	Antiproliferative activity against human Kasumi-1 cells measured after 168 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay Antiproliferative activity against human Kasumi-1 cells measured after 168 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay	[PMID: 31125896]
KG-1	IC₅₀	0.007 μM Compound: 3; CC-885	Antiproliferative activity against human KG-1 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay Antiproliferative activity against human KG-1 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
KG-1a	IC₅₀	0.008 μM Compound: 3; CC-885	Antiproliferative activity against human KG-1a cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay Antiproliferative activity against human KG-1a cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
MCF-10A	IC₅₀	0.005 μM Compound: CC-885	Cytotoxicity against human MCF10A cells after 72 hrs by MTS assay Cytotoxicity against human MCF10A cells after 72 hrs by MTS assay	[PMID: 29795767]
MM1.S	IC₅₀	0.3 nM Compound: CC-885	Antiproliferative activity against human MM1S cells measured after 168 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay Antiproliferative activity against human MM1S cells measured after 168 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay	[PMID: 31125896]
MOLM-13	IC₅₀	0.008 μM Compound: 3; CC-885	Antiproliferative activity against human MOLM-13 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay Antiproliferative activity against human MOLM-13 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
MV4-11	IC₅₀	0.005 μM Compound: 3; CC-885	Antiproliferative activity against human MV4-11 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay Antiproliferative activity against human MV4-11 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
MV4-11	IC₅₀	0.2 nM Compound: CC-885	Antiproliferative activity against human MV411 cells measured after 168 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay Antiproliferative activity against human MV411 cells measured after 168 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay	[PMID: 31125896]
MV4-11	IC₅₀	0.3 nM Compound: CC-885	Antiproliferative activity against human MV411 cells after 72 hrs by MTS assay Antiproliferative activity against human MV411 cells after 72 hrs by MTS assay	[PMID: 29795767]
NB-4	IC₅₀	0.002 μM Compound: 3; CC-885	Antiproliferative activity against human NB4 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay Antiproliferative activity against human NB4 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
OCI-AML2	IC₅₀	0.021 μM Compound: 3; CC-885	Antiproliferative activity against human OCI-AML2 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay Antiproliferative activity against human OCI-AML2 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
OCI-AML-3	IC₅₀	0.073 μM Compound: 3; CC-885	Antiproliferative activity against human OCI-AML3 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay Antiproliferative activity against human OCI-AML3 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
PBMC	IC₅₀	0.3 nM Compound: CC-885	Cytotoxicity against human PBMC cells by CellTiter96 Aqueous non-radioactive cell proliferation assay Cytotoxicity against human PBMC cells by CellTiter96 Aqueous non-radioactive cell proliferation assay	[PMID: 31125896]
Raji	IC₅₀	20.4 nM Compound: CC-885	Antiproliferative activity against human Raji cells measured after 168 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay Antiproliferative activity against human Raji cells measured after 168 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay	[PMID: 31125896]
RPMI-8226	IC₅₀	5.5 nM Compound: CC-885	Antiproliferative activity against human RPMI8226 cells measured after 72 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay Antiproliferative activity against human RPMI8226 cells measured after 72 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay	[PMID: 31125896]
SNU-C4	CC₅₀	440 nM Compound: CC-885	Cytotoxicity against PXR knock in human SNU-C4 cells measured after 72 hrs by celltiter-glo assay Cytotoxicity against PXR knock in human SNU-C4 cells measured after 72 hrs by celltiter-glo assay	[PMID: 35978691]
THLE-2	IC₅₀	0.011 μM Compound: 3; CC-885	Cytotoxicity against human THLE-2 cells assessed as cell viability incubated for 72 hrs by cell titer glo assay Cytotoxicity against human THLE-2 cells assessed as cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
THP-1	IC₅₀	1.5 nM Compound: CC-885	Antiproliferative activity against human THP1 cells measured after 168 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay Antiproliferative activity against human THP1 cells measured after 168 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay	[PMID: 31125896]
U-266	IC₅₀	2 nM Compound: CC-885	Antiproliferative activity against human U266 cells measured after 72 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay Antiproliferative activity against human U266 cells measured after 72 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay	[PMID: 31125896]
U-937	IC₅₀	0.011 μM Compound: 3; CC-885	Antiproliferative activity against human U937 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay Antiproliferative activity against human U937 cells assessed as reduction in cell viability incubated for 72 hrs by cell titer glo assay	[PMID: 33591756]
WI-38	IC₅₀	> 20 μM Compound: CC-885	Cytotoxicity against human WI38 cells after 72 hrs by MTS assay Cytotoxicity against human WI38 cells after 72 hrs by MTS assay	[PMID: 29795767]
Z-138	IC₅₀	0.4 nM Compound: CC-885	Antiproliferative activity against human Z138 cells measured after 72 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay Antiproliferative activity against human Z138 cells measured after 72 hrs by CellTiter96 Aqueous non-radioactive cell proliferation assay	[PMID: 31125896]

In Vitro

Acute myeloblatlic leukemia (AML) cell lines, human liver epithelial cell line (THLE-2) and human peripheral blood mononuclear cells (PBMC) are treated with varying concentrations of CC-885, with IC₅₀s of 10×^-6-1 μM. The effect of CC-885 on cell proliferation in AML cell lines, THLE-2 and human PBMC is more powerful than Lenalidomide and Pomalidomide with IC₅₀s>10 μM. To address whether the cereblon-dependent degradation of GSPT1 is responsible for the cytotoxic effects of CC-885, a GSPT1 mutant that retains its normal function, but loses CC-885-dependent cereblon binding, is used to distinguish the role of GSPT1 from that of other substrates. CC-885 is tested in 293T HEK cells stably expressing the CC-885-sensitive or -resistant GSPT1 variants. Overexpression of a resistant variant GSPT1Δ(1–138)/(G575N) completely abrogate the CC-885-induced anti-proliferation, whereas overexpression of a CC-885-sensitive variant GSPT1Δ(1-138) only confer partial protection. Similar results are obtained in AML cell lines^[1].

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

Molecular Weight

440.88

Formula

C₂₂H₂₁ClN₄O₄

CAS No.

1010100-07-8

Appearance

Solid

Color

White to off-white

SMILES

O=C(NCC1=CC2=C(C(N(C(CC3)C(NC3=O)=O)C2)=O)C=C1)NC4=CC=C(C)C(Cl)=C4

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Powder	-20°C	3 years
In solvent	-80°C	6 months
	-20°C	1 month

Solvent & Solubility

In Vitro:

DMSO : 66.67 mg/mL (151.22 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions

Concentration Solvent Mass	1 mg	5 mg	10 mg

1 mM	2.2682 mL	11.3410 mL	22.6819 mL
5 mM	0.4536 mL	2.2682 mL	4.5364 mL
10 mM	0.2268 mL	1.1341 mL	2.2682 mL

View the Complete Stock Solution Preparation Table

* 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. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Molarity Calculator
Dilution Calculator

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

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

Concentration _(start)

Volume _(start)

Concentration _(final)

Volume _(final)

In Vivo:

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

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: 2.25 mg/mL (5.10 mM); Suspended solution; Need ultrasonic

This protocol yields a suspended solution of 2.25 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 (22.5 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.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Protocol 2

Add each solvent one by one: 10% DMSO 90% Corn Oil
Solubility: ≥ 2.25 mg/mL (5.10 mM); Clear solution

This protocol yields a clear solution of ≥ 2.25 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 (22.5 mg/mL) to 900 μL Corn oil, and mix evenly.

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

Dosing volume
(per animal)

μL

Number of animals

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

Please enter your animal formula composition:

DMSO +

Tween-80 +

Saline

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

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).

Calculation results:

Working solution concentration: mg/mL

Method for preparing stock solution: mg drug dissolved in μL DMSO (Stock solution concentration: mg/mL).

The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).

Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.

If the continuous dosing period exceeds half a month, please choose this protocol carefully.

Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.

Purity & Documentation

Purity: 99.85%

Select Batch:

Data Sheet (273 KB) SDS (393 KB)

COA (245 KB) LCMS (93 KB)

Handling Instructions (2659 KB)

References

[1]. Mary E. Matyskiela, et al. A novel cereblon modulator recruits GSPT1 to the CRL4CRBN ubiquitin ligase. Nature. 2016 Jul 14;535(7611):252-7. [Content Brief]

[2]. Jochem M, et al. Degradome analysis to identify direct protein substrates of small-molecule degraders[J]. bioRxiv, 2024: 2024.01. 28.577572.

Cell Assay
^[1]

Human cancer cell lines cultured in the growth medium are seeded into black 384-well plates containing DMSO or test compounds such as CC-885 (10×^-6-1 μM). The seeding density for each cell line is optimized to allow the cell growth in the linear range during a 3-day culture period. To test the compound effect on cell proliferation in acute myeloid leukaemia (AML) cell lines, 5,000 to 10,000 cells per well in 200 μl complete culture media are seeded into black 96-well plates containing DMSO or test compounds such as CC-885. After 48 or 72 h, cell proliferation is assessed using the CellTiter-Glo (CTG) Luminescent Cell Viability Assay^[1].

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

References

[1]. Mary E. Matyskiela, et al. A novel cereblon modulator recruits GSPT1 to the CRL4CRBN ubiquitin ligase. Nature. 2016 Jul 14;535(7611):252-7. [Content Brief]

[2]. Jochem M, et al. Degradome analysis to identify direct protein substrates of small-molecule degraders[J]. bioRxiv, 2024: 2024.01. 28.577572.

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg

DMSO	1 mM	2.2682 mL	11.3410 mL	22.6819 mL	56.7048 mL
	5 mM	0.4536 mL	2.2682 mL	4.5364 mL	11.3410 mL
	10 mM	0.2268 mL	1.1341 mL	2.2682 mL	5.6705 mL
	15 mM	0.1512 mL	0.7561 mL	1.5121 mL	3.7803 mL
	20 mM	0.1134 mL	0.5670 mL	1.1341 mL	2.8352 mL
	25 mM	0.0907 mL	0.4536 mL	0.9073 mL	2.2682 mL
	30 mM	0.0756 mL	0.3780 mL	0.7561 mL	1.8902 mL
	40 mM	0.0567 mL	0.2835 mL	0.5670 mL	1.4176 mL
	50 mM	0.0454 mL	0.2268 mL	0.4536 mL	1.1341 mL
	60 mM	0.0378 mL	0.1890 mL	0.3780 mL	0.9451 mL
	80 mM	0.0284 mL	0.1418 mL	0.2835 mL	0.7088 mL
	100 mM	0.0227 mL	0.1134 mL	0.2268 mL	0.5670 mL

CC-885 Related Classifications

Help & FAQs

Do most proteins show cross-species activity?
Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

CC-8851010100-07-8CC885CC 885Molecular GluesLigands for E3 LigaseE3 ligase-recruiting MoietyInhibitorinhibitorinhibit

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CC-885

Customer Review

CC-885 Related Antibodies

12 Publications Citing Use of MCE CC-885

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Biological Activity

Protocol

Purity & Documentation

References

Customer Review

CC-885 Related Antibodies

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Dilution Calculator

Complete Stock Solution Preparation Table

CC-885 Related Classifications

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