UCSF

ZINC00057060

Substance Information

In ZINC since Heavy atoms Benign functionality
July 23rd, 2004 17 Yes

CAS Numbers: 66-77-3 , 73-31-4 , 73-31-4; 8041-44-9 , [73-31-4]

Other Names:

"Melatonin, 99%"

0E2B08C1-B325-45B1-8939-6F9081EFDFA4

3-(N-Acetyl-2-aminoethyl)-5-methoxyindole

4-ACETAMIDO-4'-ISOTHIO-CYANATOSTILBENE-2,2'-DISULFONIC ACID

5-22-12-00042 (Beilstein Handbook Reference)

5-Methoxy-N-acetyltryptamine

5-methoxy-N-acetyltryptamine; 73-31-4; N-[2-(5-methoxyindol-3-yl)ethyl]acetamide; N-acetyl-5-methoxy-tryptamine; melatonin

5-Methoxy-N-acetyltryptamine; Acetamide, N-(2-(5-methoxy-1H-indol-3-yl)ethyl)-; Acetamide, N-(2-(5-methoxyindol-3-yl)ethyl)-; BRN 0205542; C13H16N2O2; CCRIS 3472; EINECS 200-797-7; LS-1623; Melatonin; Melatonine; N-(2-(5-Methoxy-1H-indol-3-yl)ethyl)acetam

5-methoxy-N-acetyltryptamine; N-[2-(5-methoxyindol-3-yl)ethyl]acetamide; melatonin; melatonine

5-Methoxy-N-acetyltryptamine;Circadin;Melatol;Melatonin;Melatonin (synth.) standard-grade;Melatonin (synth.) ultra-pure;Melatonine;Melovine;MT6;N-(2-(5-Methoxy-1H-indol-3-yl)ethyl)acetamide;N-(2-(5-Methoxyindol-3-yl)ethyl)-Acetamide;N-(2-(5-Methoxyindol-3

5-Methoxy-N-acetyltryptamine;Circadin;MT6;Melatol;Melatonin;Melatonin (synth.) standard-grade;Melatonin (synth.) ultra-pure;Melatonine;Melovine;N-(2-(5-Methoxy-1H-indol-3-yl)ethyl)acetamide;N-(2-(5-Methoxyindol-3-yl)ethyl)-Acetamide;N-(2-(5-Methoxyindol-3

73-31-4

73-31-4; C01598; Melatonin; N-Acetyl-5-methoxytryptamine

73-31-4; D08170; Melatonin; Melatonina (TN)

73-31-4; Melatonin; Prestwick_312

A4039/0172195

AB00053279

AC1L1A9Q

AC1Q4F1W

AC1Q4F1X

Acetamide, N-(2-(5-methoxy-1H-indol-3-yl)ethyl)-

Acetamide, N-(2-(5-methoxy-1H-indol-3-yl)ethyl)- (9CI)

Acetamide, N-(2-(5-methoxyindol-3-yl)ethyl)-

acetamide, N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-

Acetamide, N-[2-(5-methoxy-1H-indol-3-yl)ethyl]- (9CI)

Acetamide, N-[2-(5-methoxyindol-3-yl)ethyl]-

Acetamide, N-[2-(5-methoxyindol-3-yl)ethyl]- (6CI,8CI)

Acetamide, {N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-}

Acetamide, {N-[2-(5-methoxyindol-3-yl)ethyl]-}

AKOS000276269

BAS 01281092

BIDD:ER0618

Bio-0635

BPBio1_000590

BRD-K97530723-001-07-6

BRN 0205542

BSPBio_000536

BSPBio_003006

C01598

CAS-73-31-4

CCRIS 3472

CHEBI:16796

CHEBI:25180; CHEBI:6730; CHEBI:14577

CHEMBL45

ChemDiv2_003916

CID896

Circadin

D008550

D08170

DAP000429

DB01065

DB08189

DivK1c_000353

EINECS 200-797-7

EU-0100787

HMS1380B22

HMS1569K18

HMS1921E04

HMS2089F09

HMS501B15

HSCI1_000400

HSDB 7509

I05-0076

I10-0345

IDI1_000353

IDI1_002631

IN1244

KBio1_000353

KBio2_000665

KBio2_003233

KBio2_005801

KBio3_002226

KBioGR_000591

KBioSS_000665

L001261

LS-1623

M 5250

M-1200

M-1250

M1105

M5250_SIGMA

MEL

Mela-T

Melapure

Melatol

Melatonex

Melatonex, Melatonin

Melatonin [73-31-4]; (N-Acetyl-5-methoxytryptamine)

MELATONIN; [73-31-4]

Melatonina

Melatonina (TN)

Melatonine

Melatonine, 99%

Melovine

MFCD00005655

ML1

MLS000859594

MLS001055382

MLS001240204

MLT

MolPort-000-737-883

MT6

N -Acetyl-5-methoxytryptamine

N -[2-(5-Methoxy-1 H -indol-3-yl)ethyl]acetamide

N-(2-(5-Methoxy-1H-indol-3-yl)ethyl)acetamide

N-(2-(5-Methoxyindol-3-yl)ethyl)acetamide

N-acetyl-5-methoxy-tryptamine

N-acetyl-5-methoxytryptamine

N-[2-(5-Methoxy-1H-indol-3-yl)-ethyl]-acetamide

N-[2-(5-Methoxy-1H-indol-3-yl)ethyl]acetamide

N-[2-(5-methoxyindol-3-yl)ethyl]acetamide

Nature'S Harmony

NCGC00015680-01

NCGC00015680-02

NCGC00015680-03

NCGC00015680-06

NCGC00015680-13

NCGC00090727-01

NCGC00090727-02

NCGC00090727-03

NCGC00090727-04

NCGC00090727-05

NCGC00090727-06

NCGC00090727-07

NCGC00090727-08

NCGC00090727-09

NCI60_004378

Night Rest

NINDS_000353

NMR/14327425

NSC 113928

NSC113928

NSC56423

Oprea1_104553

Oprea1_814234

OR-1465

Pineal Hormone

Posidorm

Prestwick0_000458

Prestwick1_000458

Prestwick2_000458

Prestwick3_000458

Prestwick_312

PREVENTION 1 (MELATONIN) (PREVENTION 1)

PREVENTION 2 (MELATONIN)

PREVENTION 3 (MELATONIN)

PREVENTION 4 (MELATONIN)

PREVENTION 5 (MELATONIN)

Revital Melatonin

Rx Balance

S1204_Selleck

SDCCGMLS-0065812.P001

SDCCGMLS-0065812.P002

Sleep Right

SMP2_000309

SMR000326666

SPBio_001527

SPBio_002475

SPECTRUM1500690

Spectrum2_001344

Spectrum3_001393

Spectrum4_000066

Spectrum5_001745

Spectrum_000185

STK386880

Store at -20°C

TNP00300

UNII-JL5DK93RCL

Vivitas

WLN: T56 BMJ D2MV1 GO1

ZINC00057060

Download: MOL2 SDF SMILES Flexibase

Annotations

Vendors

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) 1.45 3.62 -14.46 2 4 0 54 232.283 4
Lo Low (pH 4.5-6) 1.11 3.72 -41.44 2 4 1 52 233.291 4
Lo Low (pH 4.5-6) 1.11 3.72 -41.43 2 4 1 52 233.291 4

Vendor Notes

Note Type Comments Provided By
ALOGPS_SOLUBILITY 1.43e-01 g/l DrugBank-approved
Mp [°C] 116 - 120 Acros Organics
MP 116.5-118 °C(lit.) Indofine
MP 118 TCI
Purity 97% Fluorochem
Purity 99% APIChem
Purity >98% Fluorochem
UniProt Database Links ACH1_YEAST; GDNF_RAT; MR1AA_DANRE; MR1AL_DANRE; MR1BA_DANRE; MR1BB_DANRE; NQO2_HUMAN; PER2_HUMAN; RORA_HUMAN; SNAT_BOVIN; SNAT_CHICK; SNAT_HUMAN; SNAT_MACMU; SNAT_MESAU; SNAT_MOUSE; SNAT_PANTR; SNAT_RAT; SNAT_SHEEP; SPRE_CHLTE; SPRE_DICDI ChEBI
mechanism Dopamine antagonist IBScreen Bioactives
Therapy Endogenous neurohormone which controls photo-periodic biological rhythms SMDC Iconix
Patent Database Links EP0951842; EP1161948; EP1174134; EP1214944; EP1541197; EP1579860; EP1591118; EP1656939; EP1661575; EP1671630; EP1741437; EP1743633; EP1745798; EP1800666; EP1935405; EP1935407; EP1938803; EP1941872; EP1952798; US2003129590; US2003129591; US2004142904; US20 ChEBI
biological_source Isol. from bovine pineal glands ZereneX Building Blocks
biological_use May influence circadian rhythms in humans IBScreen Bioactives
Target MT Receptor Selleck Chemicals
Target Others Selleck Chemicals
biological_use Potent effects on the control of seasonal reproduction in mammals IBScreen Bioactives
biological_use Product of tryptophan metabolism by the pineal gland IBScreen Bioactives IBScreen Bioactives
mechanism Prolactin antagonist IBScreen Bioactives IBScreen Bioactives
mechanism Prolactin antagonist; Dopamine antagonist ZereneX Building Blocks
Reactome Database Links REACT_15383; REACT_15538; REACT_18412; REACT_22239; REACT_22289 ChEBI
S phrase S24/25: Avoid contact with skin and eyes. Acros Organics
therap sleep induction, modifies circadian rhythm MicroSource Spectrum
biological_use Synthesis and secretion subject to photoperiodic control IBScreen Bioactives
biological_use Tumour-inhibiting props. and role in immune system under investigation IBScreen Bioactives

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
MT3-1-E Metallothionein-3 (cluster #1 Of 1), Eukaryotic Eukaryotes 65 0.59 Binding ≤ 10μM
MTR1A-1-E Melatonin Receptor 1A (cluster #1 Of 2), Eukaryotic Eukaryotes 1 0.74 Binding ≤ 10μM
MTR1B-1-E Melatonin Receptor 1B (cluster #1 Of 2), Eukaryotic Eukaryotes 1 0.74 Binding ≤ 10μM
MTR1C-1-E Melatonin Receptor 1C (cluster #1 Of 1), Eukaryotic Eukaryotes 1 0.74 Binding ≤ 10μM
NQO2-1-E Quinone Reductase 2 (cluster #1 Of 4), Eukaryotic Eukaryotes 65 0.59 Binding ≤ 10μM
MTR1A-1-E Melatonin Receptor 1A (cluster #1 Of 1), Eukaryotic Eukaryotes 23 0.63 Functional ≤ 10μM
MTR1B-1-E Melatonin Receptor 1B (cluster #1 Of 1), Eukaryotic Eukaryotes 23 0.63 Functional ≤ 10μM
MTR1C-1-E Melatonin Receptor 1C (cluster #1 Of 1), Eukaryotic Eukaryotes 23 0.63 Functional ≤ 10μM
Z50597-1-O Rattus Norvegicus (cluster #1 Of 12), Other Other 0 0.00 Functional ≤ 10μM
Z81346-1-O Melanophores (Melanophore Cells) (cluster #1 Of 1), Other Other 0 0.00 Functional ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
MTR1A_CHICK P49285 Melatonin Receptor 1A, Chick 0.176 0.80 Binding ≤ 1μM
MTR1A_HUMAN P48039 Melatonin Receptor 1A, Human 0.1 0.82 Binding ≤ 1μM
MTR1B_CHICK P51050 Melatonin Receptor 1B, Chick 0.176 0.80 Binding ≤ 1μM
MTR1B_HUMAN P49286 Melatonin Receptor 1B, Human 0.1 0.82 Binding ≤ 1μM
MTR1C_CHICK P49288 Melatonin Receptor 1C, Chick 0.176 0.80 Binding ≤ 1μM
MT3_HUMAN P25713 Metallothionein-3, Human 64.6 0.59 Binding ≤ 1μM
NQO2_HUMAN P16083 Quinone Reductase 2, Human 27.6 0.62 Binding ≤ 1μM
MTR1A_CHICK P49285 Melatonin Receptor 1A, Chick 0.176 0.80 Binding ≤ 10μM
MTR1A_HUMAN P48039 Melatonin Receptor 1A, Human 0.1 0.82 Binding ≤ 10μM
MTR1B_CHICK P51050 Melatonin Receptor 1B, Chick 0.176 0.80 Binding ≤ 10μM
MTR1B_HUMAN P49286 Melatonin Receptor 1B, Human 0.1 0.82 Binding ≤ 10μM
MTR1C_CHICK P49288 Melatonin Receptor 1C, Chick 0.176 0.80 Binding ≤ 10μM
MT3_HUMAN P25713 Metallothionein-3, Human 64.6 0.59 Binding ≤ 10μM
NQO2_HUMAN P16083 Quinone Reductase 2, Human 27.6 0.62 Binding ≤ 10μM
Z81346 Z81346 Melanophores (Melanophore Cells) 0.1 0.82 Functional ≤ 10μM
MTR1A_CHICK P49285 Melatonin Receptor 1A, Chick 22.6 0.63 Functional ≤ 10μM
MTR1A_HUMAN P48039 Melatonin Receptor 1A, Human 0.1 0.82 Functional ≤ 10μM
MTR1B_HUMAN P49286 Melatonin Receptor 1B, Human 0.1 0.82 Functional ≤ 10μM
MTR1B_CHICK P51050 Melatonin Receptor 1B, Chick 22.6 0.63 Functional ≤ 10μM
MTR1C_CHICK P49288 Melatonin Receptor 1C, Chick 22.6 0.63 Functional ≤ 10μM
Z50597 Z50597 Rattus Norvegicus 0.1 0.82 Functional ≤ 10μM

Direct Reactome Annotations (via ChEBI)

Description Species
Class A/1 (Rhodopsin-like receptors)
G alpha (i) signalling events
Serotonin and melatonin biosynthesis

Reactome Annotations from Targets (via Uniprot)

Description Species
Class A/1 (Rhodopsin-like receptors)
G alpha (i) signalling events

Analogs ( Draw Identity 99% 90% 80% 70% )