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product-image-AAA227933_STRUCTURE13.gif Structure (Amine-PEG3-Desthiobiotin, CAS 2237234-71-6)

Pulrodemstat Biochemical

Pulrodemstat

Purity
98%
Synonyms
Pulrodemstat; N/A; Pulrodemstat biochemical
Ordering
Purity/Purification
98%
CAS
1821307-10-1
Targets&IC50
LSD1:0.25 nM (IC50)
Solubility
<1mg/ml refers to the product slightly soluble or insoluble
In vitro
Pulrodemstat (CC-90011; 5 mg/kg; oral administration; daily; for 30 days; for 30 days) treatment inhibits tumor growth in patient-derived xenograft SCLC models[1]. Pulrodemstat (once a day; for 4 days) treatment results in robust downregulation of GRP mRNA levels at 2.5 mg/kg and maximum suppression of GRP at 5 mg/kg in a SCLC human tumor xenograft (H1417) mice[1]. After i.v. administration, Pulrodemstat (Compound 11; 5 mg/kg) has systemic clearance of 32.4 mL/min/kg, elimination half-life of 2 h, and a high volume of distribution of 7.5 L/kg. Pulrodemstat (Compound 11; 5 mg/kg) is readily absorbed after oral administration with an AUC 0-24h of 1.8 uM/h, C/submax of 0.36 uM, and oral bioavailability of 32%[1]. Animal Model: BALB/c nude mice bearing small cell lung carcinoma (SCLC)[1]. Dosage: 5 mg/kg. Administration: Oral administration; daily; for 30 days. Result: Showed a tumor growth inhibition (TGI) of 78% at 5 mg/kg with no body weight loss.
Preparation and Storage
Powder: -20 degree C for 3 years
In solvent: -80 degree C for 2 years

Structure

(Amine-PEG3-Desthiobiotin, CAS 2237234-71-6)

product-image-AAA227933_STRUCTURE13.gif Structure (Amine-PEG3-Desthiobiotin, CAS 2237234-71-6)

Structure

(Amine-PEG3-Desthiobiotin, CAS 2237234-71-6)

product-image-AAA227933_STRUCTURE15.gif Structure (Amine-PEG3-Desthiobiotin, CAS 2237234-71-6)
Related Product Information for Pulrodemstat biochemical
Pulrodemstat (CC-90011) is a potent, selective, reversible and orally active inhibitor of lysine specific demethylase-1 (LSD1) with an IC 50 of 0.25 nM. Pulrodemstat is less enzymatic inhibition against LSD2, MOA-A, and MAO-B. Pulrodemstat induces acute myeloid leukemia (AML) and small cell lung cancer (SCLC) cells differentiation and has potent anticancer activity.
References
1. An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562

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Product Notes

The Pulrodemstat (Catalog #AAA227933) is a Biochemical and is intended for research purposes only. The product is available for immediate purchase. It is sometimes possible for the material contained within the vial of "Pulrodemstat, Biochemical" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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