General Information of the Compound
Compound ID
CP0040464
Compound Name
2-{4-[(2-Amino-4-hydroxy-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid
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Synonyms
Dideazafolate
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Structure
Formula
C21H21N5O6
Molecular Weight
439.428
Canonical SMILES
Nc1nc2ccc(CNc3ccc(cc3)C(=O)NC(CCC(O)=O)C(O)=O)cc2c(=O)[nH]1
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InChI
InChI=1S/C21H21N5O6/c22-21-25-15-6-1-11(9-14(15)19(30)26-21)10-23-13-4-2-12(3-5-13)18(29)24-16(20(31)32)7-8-17(27)28/h1-6,9,16,23H,7-8,10H2,(H,24,29)(H,27,28)(H,31,32)(H3,22,25,26,30)
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InChIKey
UQFCLENKCDVITL-UHFFFAOYSA-N
Physicochemical Property
logP
1.1652
Rotatable Bonds
9
Heavy Atom Count
32
Polar Areas
187.5
Hydrogen Bond Donor Count
6
Hydrogen Bond Acceptor Count
7
Complexity
32

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 135517463
SID: 15007761
ChEMBL ID
CHEMBL23977
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT01651, Dihydrofolate reductase
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000341 WIL2 Homo sapiens (Human)  1
1
IC50 = 34 nM
   TI
   LI
   LO
   TS
Protein ID: PT01883, Thymidylate synthase
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000266 L1210 Mus musculus (Mouse)  1
1
IC50 = 3400 nM
   TI
   LI
   LO
   TS
Protein ID: PT01120, Trifunctional purine biosynthetic protein adenosine-3
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000346 L-5178-Y Mus musculus (Mouse)  1
1
Ki = 2000 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( Dideazafolate )
Drug Name Dideazafolate
Target(s)
Glycinamide ribonucleotide formyltransferase (GART)
Inhibitor