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Chemical Structure| 1169562-71-3 Chemical Structure| 1169562-71-3

Structure of XL413 HCl
CAS No.: 1169562-71-3

Chemical Structure| 1169562-71-3

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XL413 HCl is a potent and selective Cdc7 inhibitor with an IC50 of 3.7 nM, > 60-fold selectivity against CK2, > 10-fold selectivity against PIM, and > 300-fold selectivity against a panel of over 100 protein kinases.

Synonyms: BMS-863233; XL413; BMS-863233 hydrochloride

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Product Details of XL413 HCl

CAS No. :1169562-71-3
Formula : C14H13Cl2N3O2
M.W : 326.18
SMILES Code : O=C1C(OC2=CC=C(Cl)C=C23)=C3N=C([C@H]4NCCC4)N1.[H]Cl
Synonyms :
BMS-863233; XL413; BMS-863233 hydrochloride
MDL No. :MFCD28023577

Safety of XL413 HCl

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of XL413 HCl

Hedgehog

Isoform Comparison

Biological Activity

Description
XL413 (BMS-863233) hydrochloride is an orally active and selective CDC7 inhibitor (IC50=3.4 nM). XL413 hydrochloride exhibits favorable pharmacokinetic profiles and effectively suppresses tumor growth in rodent models. XL413 hydrochloride serves as a valuable tool in cancer research [1].
Target
  • Cdc

    Cdc7, IC50:3.4 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
HeLa cells 10 µM 2 hours Test the effect of XL413 on the phosphorylation of Mcm4 in HeLa cells, showing that XL413 suppressed the phosphorylation of chromatin-bound Mcm4 as well as Mcm2 at S40 and S53. Cell Rep. 2017 Mar 7;18(10):2508-2520.
K562 cells 33 µM 24 hours Increase the efficiency of homology-directed repair (HDR), HDR increased by 1.8-fold Nat Commun. 2020 Apr 30;11(1):2109.
K562 cells 10 µM 24 hours Optimize CDC7 inhibition, explore the impact of different exposure timing on HDR Nat Commun. 2020 Apr 30;11(1):2109.
A375 cells 1 µM 24 hours XL413 treatment inhibited the short-term survival and long-term growth of A375 cells and significantly inhibited cell growth in soft agar. iScience. 2022 Jul 15;25(8):104752.
M14 cells 1 µM 24 hours XL413 treatment inhibited the short-term survival and long-term growth of M14 cells and significantly inhibited cell growth in soft agar. iScience. 2022 Jul 15;25(8):104752.
SKMEL-239 cells 1 µM 24 hours XL413 treatment inhibited the short-term survival and long-term growth of SKMEL-239 cells and significantly inhibited cell growth in soft agar. iScience. 2022 Jul 15;25(8):104752.
SKOV-3 cells 10.0 µM 36 hours Evaluate the cell viability inhibition rate of sequential treatment with XL413 and carboplatin, results showed that sequential treatment with CBP followed by XL413 significantly increased the inhibition rate Transl Oncol. 2024 Jan;39:101825.
OVCAR-3 cells 10.0 µM 36 hours Evaluate the cell viability inhibition rate of sequential treatment with XL413 and carboplatin, results showed that sequential treatment with CBP followed by XL413 significantly increased the inhibition rate Transl Oncol. 2024 Jan;39:101825.
Xenopus egg extracts 100 µM 40 minutes Evaluate the effect of XL413 on the phosphorylation of Mcm4 and Mcm2, showing that XL413 only delayed the hyper-phosphorylation of Mcm4 but efficiently inhibited the phosphorylation of Mcm2 at S40 and S53. Cell Rep. 2017 Mar 7;18(10):2508-2520.
H69-AR cells 50 µM 48 hours To evaluate the synergistic effect of XL413 with chemotherapy, the results showed that the combination of XL413 and chemotherapy significantly inhibited cell growth. Cell Death Discov. 2023 Feb 2;9(1):40.
H446-DDP cells 80 µM 48 hours To evaluate the synergistic effect of XL413 with chemotherapy, the results showed that the combination of XL413 and chemotherapy significantly inhibited cell growth. Cell Death Discov. 2023 Feb 2;9(1):40.

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Nude mice H69-AR xenograft model Intraperitoneally 20 mg/kg Administered on day 1, 3, and 5 of each cycle for 3 cycles, each cycle lasting 7 days To evaluate the synergistic effect of XL413 with chemotherapy, the results showed that the combined treatment significantly inhibited tumor growth. Cell Death Discov. 2023 Feb 2;9(1):40.
Mice OVCAR8 tumor xenograft and PDX mouse models, HGS1 mouse model Intraperitoneal injection 40 mg/kg Every 2 days Enhancement of anti-tumor immunity and improved therapeutic outcomes. Adv Sci (Weinh). 2024 Dec;11(45):e2403782
BALB/c Nude mice Subcutaneous and intraperitoneal tumor models Oral gavage 50 mg/kg 5 days per week for 3 weeks Evaluate the in vivo efficacy of sequential treatment with carboplatin and XL413 against ovarian cancer, results showed that sequential treatment significantly inhibited tumor growth and prolonged survival Transl Oncol. 2024 Jan;39:101825.
Nude mice Athymic nude mice Intraperitoneal injection 50 mg/kg Every other day until the end of the experimental period XL413 treatment inhibited melanoma tumor growth and metastasis in mice. iScience. 2022 Jul 15;25(8):104752.
C57BL/6 mice Orthotopic xenograft model Oral 50 mg/kg 6 days per week Limited tumor growth and prolonged mouse survival. Int J Biol Sci. 2023 Jul 3;19(11):3412-3427

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.07mL

0.61mL

0.31mL

15.33mL

3.07mL

1.53mL

30.66mL

6.13mL

3.07mL

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