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XLR11 N-(4-hydroxypentyl) metabolite (CRM)

CAS No.
1782099-36-8
Chemical Name:
XLR11 N-(4-hydroxypentyl) metabolite (CRM)
Synonyms
4-Hydroxypentyl XLR11;XLR-11 4-hydroxypentyl metabolite;XLR11 N-(4-hydroxypentyl) metabolite;XLR11 N-(4-hydroxypentyl) metabolite RM;XLR11 N-(4-hydroxypentyl) metabolite (CRM);[1-(5-fluoro-4-hydroxypentyl)indol-3-yl]-(2,2,3,3-tetramethylcyclopropyl)methanone;Methanone, [1-(5-fluoro-4-hydroxypentyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-
CBNumber:
CB43152773
Molecular Formula:
C21H28FNO2
Molecular Weight:
345.45
MDL Number:
MOL File:
1782099-36-8.mol
Last updated:2023-06-08 09:03:09

XLR11 N-(4-hydroxypentyl) metabolite (CRM) Properties

Boiling point 490.0±40.0 °C(Predicted)
Density 1.14±0.1 g/cm3(Predicted)
pka 13.88±0.20(Predicted)

XLR11 N-(4-hydroxypentyl) metabolite (CRM) price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 17727 XLR11 N-(4-hydroxypentyl) metabolite (CRM) 1782099-36-8 1mg $117 2024-03-01 Buy
AK Scientific 3857EB XLR11N-(4-hydroxypentyl)metabolite 1782099-36-8 1mg $228 2021-12-16 Buy
Product number Packaging Price Buy
17727 1mg $117 Buy
3857EB 1mg $228 Buy

XLR11 N-(4-hydroxypentyl) metabolite (CRM) Chemical Properties,Uses,Production

Description

XLR11 is a synthetic cannabinoid (CB) featuring a tetramethylcyclopropyl group, which reportedly confers selectivity for the peripheral CB2 receptor over the central CB1 receptor.1 XLR11 also has an N-(5-fluoropentyl) chain, which increases binding to both CB receptors.2 XLR11 N-(4-hydroxypentyl) metabolite is an expected phase I metabolite of XLR11, based on the known metabolism of similar compounds.3,4 The physiological properties of this compound have not been evaluated. This product is intended for forensic and research applications.

Uses

4-Hydroxypentyl XLR11 is a metabolite of XLR11 (X746300), an aminoalkylindole compound that is expected to be a cannabinoid (CB) mimetic.

Definition

ChEBI: XLR11 N-(4-hydroxypentyl) metabolite is a member of indoles.

References

1. Frost, J.M., Dart, M.J., Tietje, K.R., et al. Indol-3-ylcycloalkyl ketones: Effects of N1 substituted indole side chain variations on CB2 cannabinoid receptor activity J. Med. Chem. 53(1),295-315(2010).
2. Makriyannis, A., and Deng, H. Cannabimimetic indole derivatives US7241799B2,(2001).
3. Zhang, Q., Ma, P., Cole, R.B., et al. Identification of in vitro metabolites of JWH-015, an aminoalkylindole agonist for the peripheral cannabinoid receptor (CB2) by HPLC-MS/MS Anal. Bioanal. Chem. 386(5),1345-1355(2006).
4. Wintermeyer, A., M?ller, I., Thevis, M., et al. In vitro phase I metabolism of the synthetic cannabimimetic JWH-018 Anal. Bioanal. Chem. 398(5),2141-2153(2010).

XLR11 N-(4-hydroxypentyl) metabolite (CRM) Preparation Products And Raw materials

Raw materials

Preparation Products

XLR11 N-(4-hydroxypentyl) metabolite (CRM) Suppliers

Global( 4)Suppliers
Supplier Tel Email Country ProdList Advantage
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11289 58
Energy Chemical 021-58432009 400-005-6266 marketing@energy-chemical.com China 44941 58
XLR11 N-(4-hydroxypentyl) metabolite (CRM) [1-(5-fluoro-4-hydroxypentyl)indol-3-yl]-(2,2,3,3-tetramethylcyclopropyl)methanone XLR11 N-(4-hydroxypentyl) metabolite RM 4-Hydroxypentyl XLR11 XLR-11 4-hydroxypentyl metabolite XLR11 N-(4-hydroxypentyl) metabolite Methanone, [1-(5-fluoro-4-hydroxypentyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)- 1782099-36-8