Free shipping on all orders over $ 500

CAN508

Cat. No. M11247
CAN508  Structure
Size Price Availability Quantity
5mg USD 115  USD115 In stock
10mg USD 170  USD170 In stock
25mg USD 350  USD350 In stock
50mg USD 580  USD580 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

CAN508 was an effective AND ATP-competitive inhibitor of CDK9/cyclin T1 with IC50 of 0.35 μM. CAN508 is 38 times more selective for CDK9/cyclin T1 than other CDK/cyclin. CAN508 has antitumor activity.

Chemical Information
Molecular Weight 218.22
Formula C9H10N6O
CAS Number 140651-18-9
Solubility (25°C) DMSO ≥ 200 mg/mL
Storage 4°C, protect from light, dry, sealed
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Mohamed A Said, et al. Eur J Med Chem. Sulfonamide-based ring-fused analogues for CAN508 as novel carbonic anhydrase inhibitors endowed with antitumor activity: Design, synthesis, and in vitro biological evaluation

[2] Liandong Jing, et al. Bioorg Med Chem Lett. Discovery of novel CDK inhibitors via scaffold hopping from CAN508

[3] Martin Pisr, et al. Molecules. Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling

[4] Sonja Baumli, et al. ACS Chem Biol. The CDK9 C-helix exhibits conformational plasticity that may explain the selectivity of CAN508

[5] Vladimr Kryštof, et al. Eur J Med Chem. The selective P-TEFb inhibitor CAN508 targets angiogenesis

Related CDK Products
PF-07224826

PF-07224826 is a CDK2/4/6 inhibitor.

INCB123667

INCB123667 is a CDK2 inhibitor.

Senexin B

Senexin B is a potent, orally active CDK8/19 inhibitor with Kd values of 140 nM and 80 nM for CDK8 and CDK19, respectively.

Q901

Q901 is a CDK7 inhibitor for tumor-related studies.

NUV-422

NUV-422 is a CDK2/4/6 inhibitor that can be used in studies related to malignant gliomas.

  Catalog
Abmole Inhibitor Catalog




Keywords: CAN508 supplier, CDK, inhibitors, activators


Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2023 AbMole BioScience. All Rights Reserved.