NSC16116 - PubChem Compound - NCBI

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an image of a chemical structure CID 5351669

NSC16116; NSC-16116; CHEMBL1983854

MW:: 403.300
MF:: C₁₅H₂₂IN₃S

IUPAC name:: trimethyl-[2-[pyridin-2-yl(thiophen-2-ylmethyl)amino]ethyl]a...

Create Date:: 2006-02-02

CID:: 5351669

Summary Similar Compounds Same Parent, Connectivity Mixture/Component Compounds

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Same, Stereochemistry
Related PubChem Identical Compounds (Same, Stereochem.)
Same, Isotopes
Related PubChem Identical Compounds (Same, Isotopic)
Same, Connectivity
Related PubChem Identical Compounds (Same, Connectivity)
Same, Any Tautomer
Related PubChem Identical Compounds (Same, Any Tautomer)
Mixture/Component Compounds
Related PubChem Mixture/Component Compound
Parent Compound
Parent Compound
Same Parent
Same Parent
Same Parent, Stereochemistry
Same Parent, Stereochemistry
Same Parent, Isotopes
Same Parent, Isotopes
Same Parent, Connectivity
Same Parent, Connectivity
Same Parent, Any Tautomer
Same Parent, Any Tautomer
Similar Compounds
Related PubChem Similar Compound
PubChem Same Substances
Related PubChem Substance
BioAssays
Related BioAssays
BioAssays, Active
Related Active BioAssays
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Related Inactive BioAssays

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Mixture/Component Compounds for PubChem Compound (Select 408821) (1)
PubChem Compound
PREDICTED: Homo sapiens serpin family B member 12 (SERPINB12), transcript varian...
PREDICTED: Homo sapiens serpin family B member 12 (SERPINB12), transcript variant X3, mRNA
gi|2462561898|ref|XM_054319324.1|

Nucleotide
Gaucher disease due to saposin C deficiency
Gaucher disease due to saposin C deficiency

MedGen
Homo sapiens chromosome 5, GRCh38.p14 Primary Assembly
Homo sapiens chromosome 5, GRCh38.p14 Primary Assembly
gi|568815593|gnl|ASM:GCF_000001305| |NC_000005.10||gpp|GPC_000001297.1||gnl|NCBI_GENOMES|5

Nucleotide
RHOQ ras homolog family member Q [Homo sapiens]
RHOQ ras homolog family member Q [Homo sapiens]
Gene ID:23433

Gene

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