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문서

B-022

Bufotenine solution

Name: Bufotenine solution
Brand: CERILLIAN

1.0 mg/mL in acetonitrile, ampule of 1 mL, certified reference material, Cerilliant^®

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모든 사진(1)

About This Item

실험식(Hill 표기법):

C₁₂H₁₆N₂O

CAS Number:

487-93-4

Molecular Weight:

204.27

EC Number:

200-835-2

MDL number:

MFCD00130179

UNSPSC 코드:

41116107

PubChem Substance ID:

329773101

NACRES:

NA.24

추천 제품

Slide 1 of 9

1 of 9

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C-110

Catecholamine Mix 2 (Metanephrines) solution

Sigma-Aldrich

286583

5-Methoxytryptamine

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32126

Paraben target analyte mix solution

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S-042

Salicylic acid-d₄

Sigma-Aldrich

H8759

4-Hydroxy-3-methoxyphenylglycol sulfate potassium salt

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M-105

Methyl-D₃-malonic acid solution

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L-023

Levetiracetam-D₆ solution

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H-152

5-Hydroxyindole-2,4,6,7-d4-3-acetic-2,2-d2 acid (5-HIAA-D6) solution

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N-004

Naloxone solution

Grade

certified reference material

형태

liquid

특징

SNAP-N-SPIKE^®, SNAP-N-SHOOT^®

포장

ampule of 1 mL

제조업체/상표

Cerilliant^®

drug control

Narcotic Licence Schedule D (Switzerland); Decreto Lei 15/93: Tabela IIA (Portugal)

농도

1.0 mg/mL in acetonitrile

기술

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

응용 분야

forensics and toxicology

형식

single component solution

저장 온도

−20°C

SMILES string

OC1=CC=C(NC=C2CCN(C)C)C2=C1

InChI

1S/C12H16N2O/c1-14(2)6-5-9-8-13-12-4-3-10(15)7-11(9)12/h3-4,7-8,13,15H,5-6H2,1-2H3

InChI key

VTTONGPRPXSUTJ-UHFFFAOYSA-N

일반 설명

Bufotenine is a hallucinogenic alkaloid found in mushrooms, plants, mammals and in toads belonging to the Bufo genus. This drug is structurally similar to psilocin, a psychedelic compound found in mushrooms. This Snap-N-Spike^® Reference Solution is suitable for use in urine drug testing, clinical toxicology, or forensic analysis by LC-MS/MS or GC/MS.

법적 정보

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany

Snap-N-Shoot is a registered trademark of Cerilliant Corporation

Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

픽토그램

GHS02,GHS07

신호어

Danger

유해 및 위험 성명서

H225,H302 + H312 + H332,H319

예방조치 성명서

P210 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P312 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point (°F)

35.6 °F - closed cup

Flash Point (°C)

2 °C - closed cup

시험 성적서(COA)

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Identification of conserved aromatic residues essential for agonist binding and second messenger production at 5-hydroxytryptamine2A receptors.

B L Roth et al.

Molecular pharmacology, 52(2), 259-266 (1997-08-01)

Several models of agonist binding to G protein-coupled 5-hydroxytryptamine [5-HT] (serotonin) receptors have highlighted the potential importance of highly conserved aromatic residues for ligand binding and agonist efficacy. In this study, we tested these models by constructing and characterizing a

Effector pathway-dependent relative efficacy at serotonin type 2A and 2C receptors: evidence for agonist-directed trafficking of receptor stimulus.

K A Berg et al.

Molecular pharmacology, 54(1), 94-104 (1998-07-11)

There are many examples of a single receptor coupling directly to more than one cellular signal transduction pathway. Although traditional receptor theory allows for activation of multiple cellular effectors by agonists, it predicts that the relative degree of activation of

Identification of 5-hydroxy-tryptamine (bufotenine) in takini (Brosimumacutifolium Huber subsp. acutifolium C.C. Berg, Moraceae), a shamanic potion used in the Guiana Plateau.

Christian Moretti et al.

Journal of ethnopharmacology, 106(2), 198-202 (2006-02-04)

This paper is the first thorough analysis of takini, a hallucinogen used by the shamans of several peoples in Suriname, French Guiana, and the region east of the Para in Brazil. The drug is contained in the latex of the

High-affinity agonist binding is not sufficient for agonist efficacy at 5-hydroxytryptamine2A receptors: evidence in favor of a modified ternary complex model.

B L Roth et al.

The Journal of pharmacology and experimental therapeutics, 280(2), 576-583 (1997-02-01)

In this study, the relationship between high-affinity agonist binding and second messenger production was examined at native and mutant 5-hydroxytryptamine2A receptors. At native 5-hydroxytryptamine2A receptors all agonists, with the exception of quipazine, discriminated between high- and low-affinity states of the

Molecular basis of partial agonism: orientation of indoleamine ligands in the binding pocket of the human serotonin 5-HT2A receptor determines relative efficacy.

Barbara J Ebersole et al.

Molecular pharmacology, 63(1), 36-43 (2002-12-19)

Based on experiment and computational simulation, we present a structural explanation for the differing efficacies of indole agonists at the human serotonin 5-HT2A receptor (5HT2AR). We find that serotonin [5-hydroxytryptamine (5-HT)] forms hydrogen-bonds with Ser3.36 in helix 3 and Ser5.46

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문서

Bufotenine solution