hydroxy Search Results


95
Miltenyi Biotec mouse igg2a isotype control fitc

Mouse Igg2a Isotype Control Fitc, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 95 stars, based on 1 article reviews
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94
Toronto Research Chemicals hydroxymidazolam

Hydroxymidazolam, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
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86
Toronto Research Chemicals olmesartan
Effects of ARB s (A) and CCB s (B) on the high glucose‐induced CYP 11B2 transactivation. In (A), CYP 11B2 ‐H295R cells were incubated with either 100 mg·dL −1 d ‐glu (control), 450 mg·dL −1 d ‐glu ( d ‐glu), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 losartan ( d ‐glu + Los), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 valsartan ( d ‐glu + Val), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 <t>olmesartan</t> ( d ‐glu + Olm), or 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 candesartan ( d ‐glu + Can) for 48 h. Data represent mean ± SEM ( n = 3), percentage of control. * P < 0.01, vs. control. In (B), CYP 11B2 ‐H295R cells were incubated with either 100 mg·dL −1 d ‐glu, 450 mg·dL −1 d ‐glu, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 nifedipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 nifedipine, or 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 nifedipine for 96 h. Data represent mean ± SEM ( n = 4), percentage of 100 mg·dL −1 d ‐glu. * P < 0.01, vs. 100 mg·dL −1 d ‐glu. ** P < 0.05, vs. 450 mg·dL −1 d ‐glu. *** P < 0.01, vs. 450 mg·dL −1 d ‐glu.
Olmesartan, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
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94
Rockland Immunochemicals buffer
Effects of ARB s (A) and CCB s (B) on the high glucose‐induced CYP 11B2 transactivation. In (A), CYP 11B2 ‐H295R cells were incubated with either 100 mg·dL −1 d ‐glu (control), 450 mg·dL −1 d ‐glu ( d ‐glu), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 losartan ( d ‐glu + Los), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 valsartan ( d ‐glu + Val), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 <t>olmesartan</t> ( d ‐glu + Olm), or 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 candesartan ( d ‐glu + Can) for 48 h. Data represent mean ± SEM ( n = 3), percentage of control. * P < 0.01, vs. control. In (B), CYP 11B2 ‐H295R cells were incubated with either 100 mg·dL −1 d ‐glu, 450 mg·dL −1 d ‐glu, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 nifedipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 nifedipine, or 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 nifedipine for 96 h. Data represent mean ± SEM ( n = 4), percentage of 100 mg·dL −1 d ‐glu. * P < 0.01, vs. 100 mg·dL −1 d ‐glu. ** P < 0.05, vs. 450 mg·dL −1 d ‐glu. *** P < 0.01, vs. 450 mg·dL −1 d ‐glu.
Buffer, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
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93
Aladdin Scientific Corporation irinotecan
MZCC characterization. ( A ) UV−Vis absorbance spectra of <t>ZIF-8,</t> <t>CPT-11,</t> CCM, ZIC and ZICC. ( B ) FT-IR of CCM, CPT-11, ZIF-8, ZIC and ZICC. ( C ) XRD of CCM, ZIF-8, ZIC, ZICC and MZCC. ( D ) TEM image of ZIC, ZICC and MZCC. Scale bar: 100 nm. ( E ) Dynamic light scattering of ZIC, ZICC and MZCC. ( F ) Zeta potentials of ZIC, ZICC and MZCC. ( G ) SDS-PAGE of marker, MCM, ZICC and MZCC.
Irinotecan, supplied by Aladdin Scientific Corporation, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/irinotecan/product/Aladdin Scientific Corporation
Average 93 stars, based on 1 article reviews
irinotecan - by Bioz Stars, 2026-06
93/100 stars
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90
Toronto Research Chemicals 8 hydroxyefavirenz d 4
MZCC characterization. ( A ) UV−Vis absorbance spectra of <t>ZIF-8,</t> <t>CPT-11,</t> CCM, ZIC and ZICC. ( B ) FT-IR of CCM, CPT-11, ZIF-8, ZIC and ZICC. ( C ) XRD of CCM, ZIF-8, ZIC, ZICC and MZCC. ( D ) TEM image of ZIC, ZICC and MZCC. Scale bar: 100 nm. ( E ) Dynamic light scattering of ZIC, ZICC and MZCC. ( F ) Zeta potentials of ZIC, ZICC and MZCC. ( G ) SDS-PAGE of marker, MCM, ZICC and MZCC.
8 Hydroxyefavirenz D 4, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/8 hydroxyefavirenz d 4/product/Toronto Research Chemicals
Average 90 stars, based on 1 article reviews
8 hydroxyefavirenz d 4 - by Bioz Stars, 2026-06
90/100 stars
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90
Toronto Research Chemicals 7α hydroxy 4 cholesten 3 one d7
MZCC characterization. ( A ) UV−Vis absorbance spectra of <t>ZIF-8,</t> <t>CPT-11,</t> CCM, ZIC and ZICC. ( B ) FT-IR of CCM, CPT-11, ZIF-8, ZIC and ZICC. ( C ) XRD of CCM, ZIF-8, ZIC, ZICC and MZCC. ( D ) TEM image of ZIC, ZICC and MZCC. Scale bar: 100 nm. ( E ) Dynamic light scattering of ZIC, ZICC and MZCC. ( F ) Zeta potentials of ZIC, ZICC and MZCC. ( G ) SDS-PAGE of marker, MCM, ZICC and MZCC.
7α Hydroxy 4 Cholesten 3 One D7, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/7α hydroxy 4 cholesten 3 one d7/product/Toronto Research Chemicals
Average 90 stars, based on 1 article reviews
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90/100 stars
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92
Toronto Research Chemicals hydroxytamoxifen d5
MZCC characterization. ( A ) UV−Vis absorbance spectra of <t>ZIF-8,</t> <t>CPT-11,</t> CCM, ZIC and ZICC. ( B ) FT-IR of CCM, CPT-11, ZIF-8, ZIC and ZICC. ( C ) XRD of CCM, ZIF-8, ZIC, ZICC and MZCC. ( D ) TEM image of ZIC, ZICC and MZCC. Scale bar: 100 nm. ( E ) Dynamic light scattering of ZIC, ZICC and MZCC. ( F ) Zeta potentials of ZIC, ZICC and MZCC. ( G ) SDS-PAGE of marker, MCM, ZICC and MZCC.
Hydroxytamoxifen D5, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hydroxytamoxifen d5/product/Toronto Research Chemicals
Average 92 stars, based on 1 article reviews
hydroxytamoxifen d5 - by Bioz Stars, 2026-06
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90
Toronto Research Chemicals hydroxy bupropion
CYPs-selective metabolic pathways inhibition mediated by ticagrelor-O-Glu.
Hydroxy Bupropion, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hydroxy bupropion/product/Toronto Research Chemicals
Average 90 stars, based on 1 article reviews
hydroxy bupropion - by Bioz Stars, 2026-06
90/100 stars
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91
Toronto Research Chemicals c24 ceramide
CYPs-selective metabolic pathways inhibition mediated by ticagrelor-O-Glu.
C24 Ceramide, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/c24 ceramide/product/Toronto Research Chemicals
Average 91 stars, based on 1 article reviews
c24 ceramide - by Bioz Stars, 2026-06
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91
Croda International Plc 857130p
CYPs-selective metabolic pathways inhibition mediated by ticagrelor-O-Glu.
857130p, supplied by Croda International Plc, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/857130p/product/Croda International Plc
Average 91 stars, based on 1 article reviews
857130p - by Bioz Stars, 2026-06
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92
Croda International Plc 9z octadecenoyl sn glycero 3 phospho
CYPs-selective metabolic pathways inhibition mediated by ticagrelor-O-Glu.
9z Octadecenoyl Sn Glycero 3 Phospho, supplied by Croda International Plc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 92 stars, based on 1 article reviews
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Image Search Results


Journal: iScience

Article Title: Migration of human T cells can be differentially directed by electric fields depending on the extracellular microenvironment

doi: 10.1016/j.isci.2024.109746

Figure Lengend Snippet:

Article Snippet: Mouse IgG2a isotype control - FITC , Miltenyi Biotec , Cat#: 130-113-271 Lot: 5200908299.

Techniques: Recombinant, Control, Cell Isolation, Isolation, Software

Effects of ARB s (A) and CCB s (B) on the high glucose‐induced CYP 11B2 transactivation. In (A), CYP 11B2 ‐H295R cells were incubated with either 100 mg·dL −1 d ‐glu (control), 450 mg·dL −1 d ‐glu ( d ‐glu), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 losartan ( d ‐glu + Los), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 valsartan ( d ‐glu + Val), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 olmesartan ( d ‐glu + Olm), or 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 candesartan ( d ‐glu + Can) for 48 h. Data represent mean ± SEM ( n = 3), percentage of control. * P < 0.01, vs. control. In (B), CYP 11B2 ‐H295R cells were incubated with either 100 mg·dL −1 d ‐glu, 450 mg·dL −1 d ‐glu, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 nifedipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 nifedipine, or 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 nifedipine for 96 h. Data represent mean ± SEM ( n = 4), percentage of 100 mg·dL −1 d ‐glu. * P < 0.01, vs. 100 mg·dL −1 d ‐glu. ** P < 0.05, vs. 450 mg·dL −1 d ‐glu. *** P < 0.01, vs. 450 mg·dL −1 d ‐glu.

Journal: FEBS Open Bio

Article Title: High glucose stimulates expression of aldosterone synthase ( CYP 11B2 ) and secretion of aldosterone in human adrenal cells

doi: 10.1002/2211-5463.12277

Figure Lengend Snippet: Effects of ARB s (A) and CCB s (B) on the high glucose‐induced CYP 11B2 transactivation. In (A), CYP 11B2 ‐H295R cells were incubated with either 100 mg·dL −1 d ‐glu (control), 450 mg·dL −1 d ‐glu ( d ‐glu), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 losartan ( d ‐glu + Los), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 valsartan ( d ‐glu + Val), 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 olmesartan ( d ‐glu + Olm), or 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 candesartan ( d ‐glu + Can) for 48 h. Data represent mean ± SEM ( n = 3), percentage of control. * P < 0.01, vs. control. In (B), CYP 11B2 ‐H295R cells were incubated with either 100 mg·dL −1 d ‐glu, 450 mg·dL −1 d ‐glu, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 amlodipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 benidipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 efonidipine, 450 mg·dL −1 d ‐glu plus 0.01 μmol·L −1 nifedipine, 450 mg·dL −1 d ‐glu plus 0.1 μmol·L −1 nifedipine, or 450 mg·dL −1 d ‐glu plus 1 μmol·L −1 nifedipine for 96 h. Data represent mean ± SEM ( n = 4), percentage of 100 mg·dL −1 d ‐glu. * P < 0.01, vs. 100 mg·dL −1 d ‐glu. ** P < 0.05, vs. 450 mg·dL −1 d ‐glu. *** P < 0.01, vs. 450 mg·dL −1 d ‐glu.

Article Snippet: Olmesartan (olmesartan medoxomil) was purchased from Toronto Research Chemicals (North York, Canada).

Techniques: Incubation, Control

MZCC characterization. ( A ) UV−Vis absorbance spectra of ZIF-8, CPT-11, CCM, ZIC and ZICC. ( B ) FT-IR of CCM, CPT-11, ZIF-8, ZIC and ZICC. ( C ) XRD of CCM, ZIF-8, ZIC, ZICC and MZCC. ( D ) TEM image of ZIC, ZICC and MZCC. Scale bar: 100 nm. ( E ) Dynamic light scattering of ZIC, ZICC and MZCC. ( F ) Zeta potentials of ZIC, ZICC and MZCC. ( G ) SDS-PAGE of marker, MCM, ZICC and MZCC.

Journal: International Journal of Nanomedicine

Article Title: Engineered Cancer Cell Membrane-Functionalized Metal-Organic Frameworks for Irinotecan/Curcumin Codelivery in Colorectal Cancer: Enhanced Efficacy and Mitigated Toxicity

doi: 10.2147/IJN.S558675

Figure Lengend Snippet: MZCC characterization. ( A ) UV−Vis absorbance spectra of ZIF-8, CPT-11, CCM, ZIC and ZICC. ( B ) FT-IR of CCM, CPT-11, ZIF-8, ZIC and ZICC. ( C ) XRD of CCM, ZIF-8, ZIC, ZICC and MZCC. ( D ) TEM image of ZIC, ZICC and MZCC. Scale bar: 100 nm. ( E ) Dynamic light scattering of ZIC, ZICC and MZCC. ( F ) Zeta potentials of ZIC, ZICC and MZCC. ( G ) SDS-PAGE of marker, MCM, ZICC and MZCC.

Article Snippet: Irinotecan was purchased from Aladdin Scientific Co., Ltd. (Shanghai, China).

Techniques: SDS Page, Marker

CYPs-selective metabolic pathways inhibition mediated by ticagrelor-O-Glu.

Journal: Frontiers in Pharmacology

Article Title: Contributions of UDP-Glucuronosyltransferases to Human Hepatic and Intestinal Metabolism of Ticagrelor and Inhibition of UGTs and Cytochrome P450 Enzymes by Ticagrelor and its Glucuronidated Metabolite

doi: 10.3389/fphar.2021.761814

Figure Lengend Snippet: CYPs-selective metabolic pathways inhibition mediated by ticagrelor-O-Glu.

Article Snippet: Reference standard of ticagrelor (purity 95.0%), 7-Ethyl-10-hydroxy-camptothecin (SN-38) glucuronide (purity 97%), chenodeoxycholic acid 24-acyl-β-D-glucuronide (purity 96%), N-Acetyl serotonin β-D-glucuronide (purity 97%), mycophenolic acid β-D-glucuronide (purity 96%), 3′-azide-3′-deoxythymidine β-D-glucuronide sodium salt (purity 97%), bupropion (purity 98%), hydroxy bupropion (purity >98%), amodiaquine (purity >95%), N-Desethyl amodiaquine hydrochloride (purity >95%), 4′-hydroxylation diclofenac (purity >95%), S-mephenytoin, S - 4 - hydroxy mephenytoin (purity >98%), dextromethorphan (purity >95%), dextrorphan tartrate salt (purity >98%), and furafylline (purity >95%, internal standard) were purchased from Toronto Research Chemicals (Toronto, ON, Canada).

Techniques: Inhibition

Effects of ticagrelor-O-Glu on the activities of human CYPs enzymes. bupropion, amodiaquine, diclofenac, [S]-mephenytoin, dextromethorphan, and testosterone were used as the probe substrates for CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6 and CYP3A4, respectively. Each bar represents the mean ± S.D. of triple incubations. *, p < 0.05; ***, p < 0.001, ****, p < 0.0001. Each bar represents the mean ± S.D. of triple incubations.

Journal: Frontiers in Pharmacology

Article Title: Contributions of UDP-Glucuronosyltransferases to Human Hepatic and Intestinal Metabolism of Ticagrelor and Inhibition of UGTs and Cytochrome P450 Enzymes by Ticagrelor and its Glucuronidated Metabolite

doi: 10.3389/fphar.2021.761814

Figure Lengend Snippet: Effects of ticagrelor-O-Glu on the activities of human CYPs enzymes. bupropion, amodiaquine, diclofenac, [S]-mephenytoin, dextromethorphan, and testosterone were used as the probe substrates for CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6 and CYP3A4, respectively. Each bar represents the mean ± S.D. of triple incubations. *, p < 0.05; ***, p < 0.001, ****, p < 0.0001. Each bar represents the mean ± S.D. of triple incubations.

Article Snippet: Reference standard of ticagrelor (purity 95.0%), 7-Ethyl-10-hydroxy-camptothecin (SN-38) glucuronide (purity 97%), chenodeoxycholic acid 24-acyl-β-D-glucuronide (purity 96%), N-Acetyl serotonin β-D-glucuronide (purity 97%), mycophenolic acid β-D-glucuronide (purity 96%), 3′-azide-3′-deoxythymidine β-D-glucuronide sodium salt (purity 97%), bupropion (purity 98%), hydroxy bupropion (purity >98%), amodiaquine (purity >95%), N-Desethyl amodiaquine hydrochloride (purity >95%), 4′-hydroxylation diclofenac (purity >95%), S-mephenytoin, S - 4 - hydroxy mephenytoin (purity >98%), dextromethorphan (purity >95%), dextrorphan tartrate salt (purity >98%), and furafylline (purity >95%, internal standard) were purchased from Toronto Research Chemicals (Toronto, ON, Canada).

Techniques: