Drug Information
Drug General Information | Top | |||
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Drug ID |
D01GAR
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Former ID |
DNC013550
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Drug Name |
1-[(n-hex-1-ylamino)ethyl]-1,1-bisphosphonic acid
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Synonyms |
CHEMBL259192; [2-(Hexylamino)ethane-1,1-Diyl]bis(Phosphonic Acid); 1-[(n-hex-1-ylamino)ethyl]-1,1-bisphosphonic acid; SCHEMBL8674064; BDBM50341917; 2-(hexylamino)ethane-1,1-diyldiphosphonic acid; [2-(hexylamino)-1-phosphono-ethyl]phosphonic acid
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C8H21NO6P2
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Canonical SMILES |
CCCCCCNCC(P(=O)(O)O)P(=O)(O)O
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InChI |
1S/C8H21NO6P2/c1-2-3-4-5-6-9-7-8(16(10,11)12)17(13,14)15/h8-9H,2-7H2,1H3,(H2,10,11,12)(H2,13,14,15)
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InChIKey |
QDLXIUDMSHZYCG-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Geranyltranstransferase (FDPS) | Target Info | Inhibitor | [1] |
BioCyc | Superpathway of geranylgeranyldiphosphate biosynthesis I (via mevalonate) | |||
Superpathway of cholesterol biosynthesis | ||||
Trans, trans-farnesyl diphosphate biosynthesis | ||||
Geranylgeranyldiphosphate biosynthesis | ||||
KEGG Pathway | Terpenoid backbone biosynthesis | |||
Metabolic pathways | ||||
Biosynthesis of antibiotics | ||||
Influenza A | ||||
HTLV-I infection | ||||
NetPath Pathway | TCR Signaling Pathway | |||
Panther Pathway | Cholesterol biosynthesis | |||
Pathwhiz Pathway | Steroid Biosynthesis | |||
Reactome | Cholesterol biosynthesis | |||
Activation of gene expression by SREBF (SREBP) | ||||
WikiPathways | Activation of Gene Expression by SREBP (SREBF) | |||
SREBP signalling | ||||
Cholesterol Biosynthesis |
References | Top | |||
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REF 1 | Synthesis and biological evaluation of 2-alkylaminoethyl-1,1-bisphosphonic acids against Trypanosoma cruzi and Toxoplasma gondii targeting farnesyl... Bioorg Med Chem. 2008 Mar 15;16(6):3283-90. |
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