SGC-CBP30

Name: SGC-CBP30
Brand: MedChemExpress
SKU: HY-15826
Rating: 5.0 (20 reviews)

Cat. No.: HY-15826 Purity: 99.60%: Data Sheet
COA

SDS
Handling Instructions
FAQs
Technical Support

SGC-CBP30, a chemical probe, is a potent and highly selective CBP/p300 bromodomain (K_ds of 21 nM and 32 nM for CBP and p300, respectively) inhibitor, displaying 40-fold selectivity over the first bromodomain of BRD4 [BRD4(1)] bound. SGC-CBP30 strongly reduces secretion of IL-17A in Th17 cells and has anti-inflammatory effects.

연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.

CAS No. : 1613695-14-9

사이즈	재고	수량
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO ready for reconstitution	해외재고보유	Estimated Time of Arrival: December 31
Solution
10 mM * 1 mL in DMSO	해외재고보유	Estimated Time of Arrival: December 31
Solid
1 mg	해외재고보유	Estimated Time of Arrival: December 31
5 mg	해외재고보유	Estimated Time of Arrival: December 31
10 mg	해외재고보유	Estimated Time of Arrival: December 31
25 mg	해외재고보유	Estimated Time of Arrival: December 31
50 mg	해외재고보유	Estimated Time of Arrival: December 31
100 mg	해외재고보유	Estimated Time of Arrival: December 31
200 mg	견적 받기
500 mg	견적 받기

or 대량구매 문의

* 장바구니에 담기 전 물품의 수량을 선택해 주십시오.

This product is a controlled substance and not for sale in your territory.

고객리뷰

Based on 20 publication(s) in Google Scholar

20 Publications Citing Use of MCE SGC-CBP30

Histological Imaging/Staining

RT-PCR

Cell Proliferation/Viability Assay

ELISA

: SGC-CBP30 purchased from MedChemExpress. Usage Cited in: J Adv Res. 2024 Dec 28:S2090-1232(24)00624-6.; SGC-CBP30 (7.5 μg/mL, for 8 days) inhibits adipogenic differentiation in EBF2-overexpressing cells, as assessed by Oil Red O staining.

: SGC-CBP30 purchased from MedChemExpress. Usage Cited in: J Adv Res. 2024 Dec 28:S2090-1232(24)00624-6.; SGC-CBP30 (7.5 μg/mL, for 8 days) downregulated the expression of brown fat marker genes (BMP7, CIDEA, and PPARγ) and mitochondrial markers (PGC1α, Cox7a1, and Cox5b) induced in EBF2-overexpressing cells.

: SGC-CBP30 purchased from MedChemExpress. Usage Cited in: Blood Cancer J. 2019 Feb 11;9(2):19. [Abstract]; The combination of SGC-CBP30 (0.2 and 0.4 μM, 5 days) and Lenalidomide (10 μM, 5 days) exerted substantial synergy in reducing the viability of myeloma XG1LenRes cells.

: SGC-CBP30 purchased from MedChemExpress. Usage Cited in: Blood Cancer J. 2019 Feb 11;9(2):19. [Abstract]; Immunoblotting assays detected the changes in IRF4, MYC, and STAT3 after treatment with Lenalidomide （10 μM） or SGC-CBP30 (0.2 and 0.4 μM) alone or in combination (day 3).

: SGC-CBP30 purchased from MedChemExpress. Usage Cited in: Blood Cancer J. 2019 Feb 11;9(2):19. [Abstract]; SGC-CBP30 (0.2 and 0.4 μM, 2 days) treatment also reduced autocrine IL-6 production in XG1LenRes cells, both in the absence and presence of Lenalidomide (10 μM, 2 days).

Featured Recommendations

•Related Screening Libraries:

•Related Small Molecules:

•Related Proteins:

View All Histone Acetyltransferase Isoform Specific Products:

View All Isoforms

CBP/p300 GCN5/PCAF TIP60 MOZ/MORF HBO1

Biological Activity
순도&문서
References
고객리뷰

제품 설명

IC₅₀ & Target

CBP/p300

Cellular Effect

Cell Line	Type	Value	Description	References
CWR22R	IC₅₀	>10 3 Compound: CBP30	Antiproliferative activity against human 22Rv1 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human 22Rv1 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
CWR22R	IC₅₀	> 10 3 Compound: CBP30	Antiproliferative activity against human 22Rv1 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human 22Rv1 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
HEK293	IC₅₀	2.8 3 Compound: 2; SGC-CBP30	Inhibition of Halo-tagged histone H3.3 binding to NanoLuc luciferase conjugated CBP (unknown origin) expressed in HEK293 cells after overnight incubation by BRET assay Inhibition of Halo-tagged histone H3.3 binding to NanoLuc luciferase conjugated CBP (unknown origin) expressed in HEK293 cells after overnight incubation by BRET assay	[PMID: 27682507]
HEK293	IC₅₀	2.8 3 Compound: 2; SGC-CBP30	Inhibition of Halo-tagged histone H3.3 binding to NanoLuc luciferase conjugated CBP (unknown origin) expressed in HEK293 cells after overnight incubation by BRET assay Inhibition of Halo-tagged histone H3.3 binding to NanoLuc luciferase conjugated CBP (unknown origin) expressed in HEK293 cells after overnight incubation by BRET assay	[PMID: 27682507]
MCF7	IC₅₀	2.39 3 Compound: CBP30	Antiproliferative activity against human MCF7 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human MCF7 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
MCF7	IC₅₀	2.39 3 Compound: CBP30	Antiproliferative activity against human MCF7 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human MCF7 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
MOLM-13	IC₅₀	1.53 3 Compound: CBP30	Cytotoxicity against human MOLM-13 cells assessed as cell growth inhibition incubated for 5 days by CellTiter-Glo luminescence assay Cytotoxicity against human MOLM-13 cells assessed as cell growth inhibition incubated for 5 days by CellTiter-Glo luminescence assay	[PMID: 33872011]
MOLM-13	IC₅₀	1.53 3 Compound: CBP30	Cytotoxicity against human MOLM-13 cells assessed as cell growth inhibition incubated for 5 days by CellTiter-Glo luminescence assay Cytotoxicity against human MOLM-13 cells assessed as cell growth inhibition incubated for 5 days by CellTiter-Glo luminescence assay	[PMID: 33872011]
OPM-2	IC₅₀	2.64 3 Compound: CBP30	Antiproliferative activity against human OPM-2 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human OPM-2 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
OPM-2	IC₅₀	2.64 3 Compound: CBP30	Antiproliferative activity against human OPM-2 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human OPM-2 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
CWR22R	IC₅₀	> 10 3 Compound: CBP30	Antiproliferative activity against human 22Rv1 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human 22Rv1 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
RKO	IC₅₀	1.5 3 Compound: 11; SGC-CBP30	Inhibition of doxorubicin-stimulated p53 (unknown origin) expressed in human RKO cells preincubated for 24 hrs followed by addition of doxorubicin for 16 hrs by luciferase reporter assay Inhibition of doxorubicin-stimulated p53 (unknown origin) expressed in human RKO cells preincubated for 24 hrs followed by addition of doxorubicin for 16 hrs by luciferase reporter assay	[PMID: 26572217]
RKO	IC₅₀	1.5 3 Compound: 11; SGC-CBP30	Inhibition of doxorubicin-stimulated p53 (unknown origin) expressed in human RKO cells preincubated for 24 hrs followed by addition of doxorubicin for 16 hrs by luciferase reporter assay Inhibition of doxorubicin-stimulated p53 (unknown origin) expressed in human RKO cells preincubated for 24 hrs followed by addition of doxorubicin for 16 hrs by luciferase reporter assay	[PMID: 26572217]
HEK293	IC₅₀	2.8 3 Compound: 2; SGC-CBP30	Inhibition of Halo-tagged histone H3.3 binding to NanoLuc luciferase conjugated CBP (unknown origin) expressed in HEK293 cells after overnight incubation by BRET assay Inhibition of Halo-tagged histone H3.3 binding to NanoLuc luciferase conjugated CBP (unknown origin) expressed in HEK293 cells after overnight incubation by BRET assay	[PMID: 27682507]
SCC-9	IC₅₀	6.42 3 Compound: CBP30	Antiproliferative activity against human SCC-9 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human SCC-9 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
SCC-9	IC₅₀	6.42 3 Compound: CBP30	Antiproliferative activity against human SCC-9 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human SCC-9 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
MCF7	IC₅₀	2.39 3 Compound: CBP30	Antiproliferative activity against human MCF7 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human MCF7 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
MOLM-13	IC₅₀	1.53 3 Compound: CBP30	Cytotoxicity against human MOLM-13 cells assessed as cell growth inhibition incubated for 5 days by CellTiter-Glo luminescence assay Cytotoxicity against human MOLM-13 cells assessed as cell growth inhibition incubated for 5 days by CellTiter-Glo luminescence assay	[PMID: 33872011]
OPM-2	IC₅₀	2.64 3 Compound: CBP30	Antiproliferative activity against human OPM-2 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human OPM-2 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]
RKO	IC₅₀	1.5 3 Compound: 11; SGC-CBP30	Inhibition of doxorubicin-stimulated p53 (unknown origin) expressed in human RKO cells preincubated for 24 hrs followed by addition of doxorubicin for 16 hrs by luciferase reporter assay Inhibition of doxorubicin-stimulated p53 (unknown origin) expressed in human RKO cells preincubated for 24 hrs followed by addition of doxorubicin for 16 hrs by luciferase reporter assay	[PMID: 26572217]
SCC-9	IC₅₀	6.42 3 Compound: CBP30	Antiproliferative activity against human SCC-9 cells incubated for 5 days by CCK-8 method Antiproliferative activity against human SCC-9 cells incubated for 5 days by CCK-8 method	[PMID: 35569250]

In Vitro

In ankylosing spondylitis and psoriatic arthritis condition, SGC-CBP30 inhibits IL-17A secretion by Th17 cells. Transcriptional profiling of human T cells after SGC-CBP30 treatment shows a much more restricted effect on gene expression than that observed with the pan-BET (bromo and extraterminal domain protein family) bromodomain inhibitor JQ1^[1].

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

In Vivo

SGC-CBP30 treatment slightly alleviates alveolar bronchial fibrosis induced by NSC-125066. SGC-CBP30 plus CQ-061 dramatically reduces alveolar bronchial fibrosis. The ELISA of cytokines IL-4 and IFN-γ in BALF demonstrates that combination of SGC-CBP300 and CQ-061 suppresses the activation of IL-4 as well as IFN-γ in NSC-125066 induced IPF murine models to nearly normal levels^[2].

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

Animal Model:	Sprague-Dawley (SD) rats (aged 3-4 weeks) injected with NSC-125066^[2]
Dosage:	25 mg/kg
Administration:	Oral administration; daily; for 14 days
Result:	Slightly alleviated alveolar bronchial fibrosis induced by NSC-125066.

분자량

509.04

화학식

C₂₈H₃₃ClN₄O₃

CAS No.

1613695-14-9

Appearance

Solid

Color

White to yellow

SMILES

C[C@H](N1CCOCC1)CN2C(CCC3=CC=C(OC)C(Cl)=C3)=NC4=CC(C5=C(C)ON=C5C)=CC=C42

선적

Room temperature in continental US; may vary elsewhere.

보관

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

용액&용해도

In Vitro:

DMSO : 66.67 mg/mL (130.97 mM; ultrasonic and warming and heat to 60°C; 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	1.9645 mL	9.8224 mL	19.6448 mL
5 mM	0.3929 mL	1.9645 mL	3.9290 mL
10 mM	0.1964 mL	0.9822 mL	1.9645 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, 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.

몰농도 계산기
농도 희석 계산기

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: ≥ 2.5 mg/mL (4.91 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 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.
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: ≥ 2.5 mg/mL (4.91 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 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 (25.0 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.

순도&문서

Purity: 99.83%

Select Batch:

Data Sheet (277 KB) SDS (396 KB)

COA (251 KB) LCMS (137 KB)

Handling Instructions (2659 KB)

References

[1]. Hammitzsch A, et al. CBP30, a selective CBP/p300 bromodomain inhibitor, suppresses human Th17 responses. Proc Natl Acad Sci U S A. 2015 Aug 25;112(34):10768-73. [Content Brief]

[2]. Tao J, Inhibition of EP300 and DDR1 synergistically alleviates pulmonary fibrosis in vitro and in vivo. Biomed Pharmacother. 2018 Oct;106:1727-1733. [Content Brief]

[3]. Hay DA, et al. Discovery and optimization of small-molecule ligands for the CBP/p300 bromodomains. J Am Chem Soc. 2014 Jul 2;136(26):9308-19. [Content Brief]

Complete Stock Solution Preparation Table

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

DMSO	1 mM	1.9645 mL	9.8224 mL	19.6448 mL	49.1121 mL
	5 mM	0.3929 mL	1.9645 mL	3.9290 mL	9.8224 mL
	10 mM	0.1964 mL	0.9822 mL	1.9645 mL	4.9112 mL
	15 mM	0.1310 mL	0.6548 mL	1.3097 mL	3.2741 mL
	20 mM	0.0982 mL	0.4911 mL	0.9822 mL	2.4556 mL
	25 mM	0.0786 mL	0.3929 mL	0.7858 mL	1.9645 mL
	30 mM	0.0655 mL	0.3274 mL	0.6548 mL	1.6371 mL
	40 mM	0.0491 mL	0.2456 mL	0.4911 mL	1.2278 mL
	50 mM	0.0393 mL	0.1964 mL	0.3929 mL	0.9822 mL
	60 mM	0.0327 mL	0.1637 mL	0.3274 mL	0.8185 mL
	80 mM	0.0246 mL	0.1228 mL	0.2456 mL	0.6139 mL
	100 mM	0.0196 mL	0.0982 mL	0.1964 mL	0.4911 mL

SGC-CBP30 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:

SGC-CBP301613695-14-9Epigenetic Reader DomainHistone AcetyltransferaseHATsHATBRDankylosingspondylitispsoriaticarthritisTh17cellsIL-17Aanti-inflammatoryepigeneticInhibitorinhibitorinhibit

Please select a local distributor ナミキ商事株式会社コスモ・バイオ株式会社重松貿易株式会社
상품명			Requested Quantity *
고객명 *			호칭
메일주소 *			전화번호 *
Department			회사명 *
City			도
Country or Region *
비고

상품명			Lot #
고객명 *			메일주소 *
전화번호			Department *
회사명 *			Country or Region *
비고

Name
이메일 *

	Sorry, but the email address you supplied was invalid.

SGC-CBP30

고객리뷰

SGC-CBP30 Related Antibodies

20 Publications Citing Use of MCE SGC-CBP30

Featured Recommendations

•Related Screening Libraries:

•Related Small Molecules:

•Related Proteins:

View All Histone Acetyltransferase Isoform Specific Products:

Biological Activity

순도&문서

References

고객리뷰

SGC-CBP30 Related Antibodies

몰농도 계산기

농도 희석 계산기

Complete Stock Solution Preparation Table

SGC-CBP30 Related Classifications

Keywords:

최근 본 상품:

고객리뷰

Request for HNMR Report

SAFETY DATA SHEET (SDS)

Request for HNMR Report