4-(2-(2-(4-((4-(6-(6-acetyl-8-cyclopentyl-5-methyl-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-2-ylamino)pyridin-3-yl)piperazin-1-yl)methyl)-1H-1,2,3-triazol-1-yl)ethoxy)ethylamino)-2-(1-ethyl-2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione

ID: ALA4440866

PubChem CID: 155514854

Max Phase: Preclinical

Molecular Formula: C46H53N13O7

Molecular Weight: 900.01

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CCN1C(=O)CCC(N2C(=O)c3cccc(NCCOCCn4cc(CN5CCN(c6ccc(Nc7ncc8c(C)c(C(C)=O)c(=O)n(C9CCCC9)c8n7)nc6)CC5)nn4)c3C2=O)C1=O

Standard InChI:  InChI=1S/C46H53N13O7/c1-4-57-38(61)15-13-36(43(57)63)59-42(62)33-10-7-11-35(40(33)45(59)65)47-16-22-66-23-21-56-27-30(52-53-56)26-54-17-19-55(20-18-54)32-12-14-37(48-24-32)50-46-49-25-34-28(2)39(29(3)60)44(64)58(41(34)51-46)31-8-5-6-9-31/h7,10-12,14,24-25,27,31,36,47H,4-6,8-9,13,15-23,26H2,1-3H3,(H,48,49,50,51)

Standard InChI Key:  SHXGVEVMTPMRSW-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

 66 74  0  0  0  0  0  0  0  0999 V2000
    4.1414  -17.7605    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4898  -17.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9097  -18.4808    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7336  -18.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9014  -17.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7260  -17.0448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1346  -16.3306    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7196  -15.6182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8918  -15.6245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870  -16.3393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9607  -16.3249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4483  -16.9904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2319  -16.7323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2287  -15.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4431  -15.6555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1504  -19.1870    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1280  -14.9014    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4736  -14.9133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8805  -14.1956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6486  -14.9199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6619  -16.3452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9753  -19.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3887  -19.8942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2130  -19.8896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6219  -19.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2008  -18.4578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3779  -18.4659    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4441  -19.1635    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8606  -19.8767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6821  -19.8727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0932  -19.1569    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.6766  -18.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8490  -18.4461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9182  -19.1540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3332  -19.8670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0023  -20.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6173  -21.1679    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.3304  -20.7527    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.1558  -19.9465    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.6127  -21.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3247  -22.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0415  -22.0001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7536  -22.4166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4704  -22.0082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1826  -22.4248    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.8994  -22.0163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6083  -22.4334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3246  -22.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3297  -21.1998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8993  -21.1935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6104  -20.7796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4367  -19.9753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6179  -19.8921    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.2860  -20.6449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2036  -19.1842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6159  -18.4684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2044  -17.7575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3791  -17.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9668  -18.4718    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.3800  -19.1889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9668  -17.0415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9692  -19.9044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4795  -20.8192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.9867  -19.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1418  -18.4718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7292  -17.7574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  6  2  0
  5  2  2  0
  2  3  1  0
  3  4  2  0
  4  1  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10  5  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 11  1  0
  7 11  1  0
  4 16  1  0
  8 17  2  0
  9 18  1  0
 18 19  1  0
 18 20  2  0
 10 21  1  0
 16 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 22  1  0
 28 29  1  0
 28 33  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 25 28  1  0
 31 34  1  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  1  0
 38 39  2  0
 39 35  1  0
 37 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
 46 47  2  0
 47 48  1  0
 48 49  2  0
 49 51  1  0
 50 46  1  0
 50 51  2  0
 51 52  1  0
 52 53  1  0
 53 54  1  0
 54 50  1  0
 55 56  1  0
 55 60  1  0
 56 57  1  0
 57 58  1  0
 58 59  1  0
 59 60  1  0
 53 55  1  0
 58 61  2  0
 60 62  2  0
 54 63  2  0
 52 64  2  0
 59 65  1  0
 65 66  1  0
M  END

Alternative Forms

  1. Parent:

    ALA4440866

    ---

Associated Targets(Human)

CDK6 Tclin Protein cereblon/Cyclin-dependent kinase 6 (113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDK4 Tclin Protein cereblon/Cyclin-dependent kinase 4 (68 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THP-1 (11052 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MM1.S (1111 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RPMI-8226 (44974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
JeKo-1 (376 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Biocomponents

Calculated Properties

Molecular Weight: 900.01Molecular Weight (Monoisotopic): 899.4191AlogP: 3.73#Rotatable Bonds: 16
Polar Surface Area: 222.98Molecular Species: NEUTRALHBA: 18HBD: 2
#RO5 Violations: 2HBA (Lipinski): 20HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.33CX Basic pKa: 5.66CX LogP: 3.51CX LogD: 3.50
Aromatic Rings: 5Heavy Atoms: 66QED Weighted: 0.08Np Likeness Score: -1.41

References

1. Su S, Yang Z, Gao H, Yang H, Zhu S, An Z, Wang J, Li Q, Chandarlapaty S, Deng H, Wu W, Rao Y..  (2019)  Potent and Preferential Degradation of CDK6 via Proteolysis Targeting Chimera Degraders.,  62  (16): [PMID:31330105] [10.1021/acs.jmedchem.9b00871]
2. Fry, David W DW and 10 more authors.  2004-11  Specific inhibition of cyclin-dependent kinase 4/6 by PD 0332991 and associated antitumor activity in human tumor xenografts.  [PMID:15542782]
3. Squires, Matthew S MS and 7 more authors.  2009-02  Biological characterization of AT7519, a small-molecule inhibitor of cyclin-dependent kinases, in human tumor cell lines.  [PMID:19174555]
4. Cirstea, D D and 15 more authors.  2013-12  Small-molecule multi-targeted kinase inhibitor RGB-286638 triggers P53-dependent and -independent anti-multiple myeloma activity through inhibition of transcriptional CDKs.  [PMID:23807770]
5. Gelbert, Lawrence M LM and 16 more authors.  2014-10  Preclinical characterization of the CDK4/6 inhibitor LY2835219: in-vivo cell cycle-dependent/independent anti-tumor activities alone/in combination with gemcitabine.  [PMID:24919854]
6. Paiva, Cody C and 8 more authors.  2015  Cyclin-Dependent Kinase Inhibitor P1446A Induces Apoptosis in a JNK/p38 MAPK-Dependent Manner in Chronic Lymphocytic Leukemia B-Cells.  [PMID:26606677]
7. Bisi, John E JE, Sorrentino, Jessica A JA, Roberts, Patrick J PJ, Tavares, Francis X FX and Strum, Jay C JC.  2016-05  Preclinical Characterization of G1T28: A Novel CDK4/6 Inhibitor for Reduction of Chemotherapy-Induced Myelosuppression.  [PMID:26826116]
8. Wang, Yan Y and 10 more authors.  2018-03-01  Design and synthesis of 4-(2,3-dihydro-1H-benzo[d]pyrrolo[1,2-a]imidazol-7-yl)-N-(5-(piperazin-1-ylmethyl)pyridine-2-yl)pyrimidin-2-amine as a highly potent and selective cyclin-dependent kinases 4 and 6 inhibitors and the discovery of structure-activity relationships.  [PMID:29429832]
9. Zhi, Yanle Y and 9 more authors.  2018-07-15  Discovery of the selective and efficacious inhibitors of FLT3 mutations.  [PMID:29894944]

Source