2380-94-1,MFCD00005667
Catalog No.:AA0037OH

2380-94-1 | 4-Hydroxyindole

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$7.00   $5.00
- +
1g
98%(GC)
in stock  
$24.00   $17.00
- +
5g
98%
in stock  
$45.00   $32.00
- +
25g
98%
in stock  
$139.00   $97.00
- +
100g
98%
in stock  
$534.00   $374.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0037OH
Chemical Name:
4-Hydroxyindole
CAS Number:
2380-94-1
Molecular Formula:
C8H7NO
Molecular Weight:
133.1473
MDL Number:
MFCD00005667
SMILES:
Oc1cccc2c1cc[nH]2
Properties
Properties
 
BP:
343.2°C at 760 mmHg  
Form:
Solid  
MP:
97-99 °C(lit.)  
Refractive Index:
1.5260 (estimate)  
Stability:
Air Sensitive  
Storage:
Keep in dry area;-20 ℃;  

Computed Properties
 
Complexity:
126  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
2  
XLogP3:
2.4  

Literature

Title: Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.

Journal: Bioorganic & medicinal chemistry 20121115

Title: Prospective acetylcholinesterase inhibitory activity of indole and its analogs.

Journal: Bioorganic & medicinal chemistry letters 20120415

Title: Fluorescence-based high-throughput screening assay for drug interactions with UGT1A6.

Journal: Assay and drug development technologies 20111001

Title: Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20100301

Title: Bicyclic compounds repress membrane vesicle production and Pseudomonas quinolone signal synthesis in Pseudomonas aeruginosa.

Journal: FEMS microbiology letters 20100301

Title: Inhibitory effect of hydroxyindoles and their analogues on human melanoma tyrosinase.

Journal: Zeitschrift fur Naturforschung. C, Journal of biosciences 20100101

Title: Halogenated indole alkaloids from marine invertebrates.

Journal: Marine drugs 20100101

Title: Synthesis of indoleamine 2,3-dioxygenase inhibitory analogues of the sponge alkaloid exiguamine A.

Journal: Journal of medicinal chemistry 20080508

Title: Synthesis and biological evaluation of novel angular fused Pyrrolocoumarins.

Journal: Journal of enzyme inhibition and medicinal chemistry 20080201

Title: Indoloxypropanolamine analogues as 5-HT(1A) receptor antagonists.

Journal: Bioorganic & medicinal chemistry letters 20071015

Title: Inhibition of amyloid fibril formation and cytotoxicity by hydroxyindole derivatives.

Journal: Biochemistry 20060418

Title: Protein engineering of toluene ortho-monooxygenase of Burkholderia cepacia G4 for regiospecific hydroxylation of indole to form various indigoid compounds.

Journal: Applied microbiology and biotechnology 20050101

Title: Nenad Manevski, et al. Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases. Drug Metab Dispos. 2010 Mar;38(3):386-95.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:2380-94-1 Molecular Formula|2380-94-1 MDL|2380-94-1 SMILES|2380-94-1 4-Hydroxyindole
Catalog No.: AA0037OH
2380-94-1,MFCD00005667
2380-94-1 | 4-Hydroxyindole
Pack Size: 250mg
Purity: 98%
in stock
$7.00 $5.00
Pack Size: 1g
Purity: 98%(GC)
in stock
$24.00 $17.00
Pack Size: 5g
Purity: 98%
in stock
$45.00 $32.00
Pack Size: 25g
Purity: 98%
in stock
$139.00 $97.00
Pack Size: 100g
Purity: 98%
in stock
$534.00 $374.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0037OH
Chemical Name: 4-Hydroxyindole
CAS Number: 2380-94-1
Molecular Formula: C8H7NO
Molecular Weight: 133.1473
MDL Number: MFCD00005667
SMILES: Oc1cccc2c1cc[nH]2
Properties
BP: 343.2°C at 760 mmHg  
Form: Solid  
MP: 97-99 °C(lit.)  
Refractive Index: 1.5260 (estimate)  
Stability: Air Sensitive  
Storage: Keep in dry area;-20 ℃;  
Complexity: 126  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 2  
XLogP3: 2.4  
Literature fold

Title: Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.

Journal: Bioorganic & medicinal chemistry20121115

Title: Prospective acetylcholinesterase inhibitory activity of indole and its analogs.

Journal: Bioorganic & medicinal chemistry letters20120415

Title: Fluorescence-based high-throughput screening assay for drug interactions with UGT1A6.

Journal: Assay and drug development technologies20111001

Title: Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases.

Journal: Drug metabolism and disposition: the biological fate of chemicals20100301

Title: Bicyclic compounds repress membrane vesicle production and Pseudomonas quinolone signal synthesis in Pseudomonas aeruginosa.

Journal: FEMS microbiology letters20100301

Title: Inhibitory effect of hydroxyindoles and their analogues on human melanoma tyrosinase.

Journal: Zeitschrift fur Naturforschung. C, Journal of biosciences20100101

Title: Halogenated indole alkaloids from marine invertebrates.

Journal: Marine drugs20100101

Title: Synthesis of indoleamine 2,3-dioxygenase inhibitory analogues of the sponge alkaloid exiguamine A.

Journal: Journal of medicinal chemistry20080508

Title: Synthesis and biological evaluation of novel angular fused Pyrrolocoumarins.

Journal: Journal of enzyme inhibition and medicinal chemistry20080201

Title: Indoloxypropanolamine analogues as 5-HT(1A) receptor antagonists.

Journal: Bioorganic & medicinal chemistry letters20071015

Title: Inhibition of amyloid fibril formation and cytotoxicity by hydroxyindole derivatives.

Journal: Biochemistry20060418

Title: Protein engineering of toluene ortho-monooxygenase of Burkholderia cepacia G4 for regiospecific hydroxylation of indole to form various indigoid compounds.

Journal: Applied microbiology and biotechnology20050101

Title: Nenad Manevski, et al. Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases. Drug Metab Dispos. 2010 Mar;38(3):386-95.

Building Blocks More >
4492-51-7
4492-51-7
(Cyclopentylmethyl)methylamine hydrochloride
AA0037RO | MFCD07437829
3672-39-7
3672-39-7
2-Phenyl-imidazo[1,2-a]pyridine-3-carbaldehyde
AA0037UZ | MFCD00964691
35196-48-6
35196-48-6
Ethyl 2-hydrazinyl-2-oxoacetate
AA0037YB | MFCD05665958
135-48-8
135-48-8
Pentacene
AA00381F | MFCD00003710
1842-70-2
1842-70-2
Octadecanoic acid,9-oxo-, methyl ester
AA00384W | MFCD00192310
118811-34-0
118811-34-0
Carbamic acid,[5-[[(4-methylphenyl)sulfonyl]oxy]pentyl]-, 1,1-dimethylethyl ester (9CI)
AA003889 | MFCD07776967
849217-64-7
849217-64-7
Foretinib
AA0038BC | MFCD16038048
69571-02-4
69571-02-4
4,4'-Diiodo-2,2'-dimethyl-1,1'-biphenyl
AA0038EM | MFCD13185944
62821-88-9
62821-88-9
2-(3,5-Dimethyl-pyrazol-1-yl)-ethylamine
AA0038HW | MFCD04967722
5458-56-0
5458-56-0
2,4-Dichloro-5,6,7,8-tetrahydroquinazoline-6-carboxylic acid
AA0038L3 | MFCD12198785
Submit
© 2017 AA BLOCKS, INC. All rights reserved.