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18525-25-2 molecular structure
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(2Z)-but-2-enedioic acid; 3-(2-aminoethyl)-1H-indol-5-ol

ChemBase ID: 133740
Molecular Formular: C14H16N2O5
Molecular Mass: 292.28724
Monoisotopic Mass: 292.10592162
SMILES and InChIs

SMILES:
c1cc2c(cc1O)c(c[nH]2)CCN.C(=C\C(=O)O)\C(=O)O
Canonical SMILES:
OC(=O)/C=C\C(=O)O.NCCc1c[nH]c2c1cc(O)cc2
InChI:
InChI=1S/C10H12N2O.C4H4O4/c11-4-3-7-6-12-10-2-1-8(13)5-9(7)10;5-3(6)1-2-4(7)8/h1-2,5-6,12-13H,3-4,11H2;1-2H,(H,5,6)(H,7,8)/b;2-1-
InChIKey:
LTEXAUVYLLADEB-BTJKTKAUSA-N

Cite this record

CBID:133740 http://www.chembase.cn/molecule-133740.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(2Z)-but-2-enedioic acid; 3-(2-aminoethyl)-1H-indol-5-ol
IUPAC Traditional name
maleic acid; serotonin
Synonyms
Serotonin hydrogen maleate
3-(2-Aminoethyl)-5-hydroxyindole hydrogen maleate
5-HT
5-Hydroxytryptamine hydrogen maleate
3-(2-氨乙酸)吲哚 马来酸氢盐
CAS Number
18525-25-2
EC Number
242-399-6
MDL Number
MFCD00043256
Beilstein Number
8173182
PubChem SID
162228017
24895516
PubChem CID
16218591

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
H4511 external link Add to cart Please log in.
Data Source Data ID
PubChem 16218591 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 9.314034  H Acceptors
H Donor LogD (pH = 5.5) -1.8204005 
LogD (pH = 7.4) -1.0317981  Log P 0.481548 
Molar Refractivity 52.3538 cm3 Polarizability 21.302618 Å3
Polar Surface Area 62.04 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Pharmacology Properties Bioassay(PubChem)
Apperance
off-white to yellow powder expand Show data source
RTECS
NM2560000 expand Show data source
European Hazard Symbols
Harmful Harmful (Xn) expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
22 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H302 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Storage Temperature
2-8°C expand Show data source
Gene Information
human ... HTR3A(3359) expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - H4511 external link
Biochem/physiol Actions
Neurotransmitter.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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