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OAC-2 - 10mM in DMSO, high purity , CAS No.6019-39-2
Oct4 activator; enhances iPSC reprogramming efficiency
Basic Description
Synonyms
OAC2 | N-(1H-indol-5-yl)benzamide | 6019-39-2 | 5-benzoylaminoindole | N-1h-indol-5-yl-benzamide | OAC-2 | 5-Benzamidoindole | Maybridge3_002618 | Oprea1_121826 | MLS000860608 | OAC-2;OAC 2 | SCHEMBL4761937 | CHEMBL1464276 | EX-A906 | JCAFGYWSIWYMOX-UHFFFAOYSA-N | DTXSID301329745 | HMS1
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
OAC2 (Oct4 activating compound 2) is an activator of Octamer-binding transcription factor 4 (Oct4), which is involved in the self-renewal of undifferentiated embryonic stem cells, regulating embryonic stem cell pluripotency.
Storage Temp
Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Indoles and derivatives
Subclass
Indoles
Intermediate Tree Nodes
Not available
Direct Parent
Indoles
Alternative Parents
Benzamides Benzoyl derivatives Pyrroles Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Benzamide - Benzoic acid or derivatives - Indole - Benzoyl - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Pyrrole - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
N-(1H-indol-5-yl)benzamide
INCHI
InChI=1S/C15H12N2O/c18-15(11-4-2-1-3-5-11)17-13-6-7-14-12(10-13)8-9-16-14/h1-10,16H,(H,17,18)
InChIKey
JCAFGYWSIWYMOX-UHFFFAOYSA-N
Smiles
C1=CC=C(C=C1)C(=O)NC2=CC3=C(C=C2)NC=C3
Isomeric SMILES
C1=CC=C(C=C1)C(=O)NC2=CC3=C(C=C2)NC=C3
Molecular Weight
236.27
Reaxy-Rn
194144
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=194144&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Melt Point(°C)
165 - 167°C
Molecular Weight
236.270 g/mol
XLogP3
2.700
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
2
Exact Mass
236.095 Da
Monoisotopic Mass
236.095 Da
Topological Polar Surface Area
44.900 Ų
Heavy Atom Count
18
Formal Charge
0
Complexity
299.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
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