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1-((R)-1-(2,4-dichlorophenyl)ethyl)-6-((4S,5R)-4-((S)-2-(2-hydroxypropan-2-yl)pyrrolidin-1-yl)-5-methylcyclohex-1-enyl)-1H-pyrazolo[4,3-b]pyrazine-3-carbonitrile ID: ALA4555534
PubChem CID: 155557193
Max Phase: Preclinical
Molecular Formula: C28H32Cl2N6O
Molecular Weight: 539.51
Molecule Type: Unknown
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: C[C@@H]1CC(c2cnc3c(C#N)nn([C@H](C)c4ccc(Cl)cc4Cl)c3n2)=CC[C@@H]1N1CCC[C@H]1C(C)(C)O
Standard InChI: InChI=1S/C28H32Cl2N6O/c1-16-12-18(7-10-24(16)35-11-5-6-25(35)28(3,4)37)23-15-32-26-22(14-31)34-36(27(26)33-23)17(2)20-9-8-19(29)13-21(20)30/h7-9,13,15-17,24-25,37H,5-6,10-12H2,1-4H3/t16-,17-,24+,25+/m1/s1
Standard InChI Key: SMHHJJVPINEKAG-NXIIPSDBSA-N
Molfile:
RDKit 2D
37 41 0 0 0 0 0 0 0 0999 V2000
5.0235 -6.1266 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.7334 -6.5439 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4506 -6.1360 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4560 -5.3066 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.7382 -4.8868 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.0190 -5.3005 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.1727 -4.8957 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8894 -5.3177 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.6096 -4.9056 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
7.1757 -4.0699 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
7.8930 -3.6596 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.6124 -4.0733 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.2282 -3.5170 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.8895 -2.7593 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
8.0643 -2.8474 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
7.5113 -2.2353 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7649 -1.4503 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.7046 -2.4082 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.1538 -1.7926 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.3478 -1.9650 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.0935 -2.7507 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6513 -3.3642 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4552 -3.1887 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.2871 -2.9246 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0
6.4094 -1.0084 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0
4.3099 -6.5384 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
5.7277 -7.3689 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.5587 -6.2054 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.0072 -6.8174 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.4191 -7.5310 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.2249 -7.3598 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3866 -5.3986 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.0324 -3.6865 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.8396 -3.8568 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
3.9992 -4.8461 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6018 -5.1442 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.1664 -4.5954 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0
1 6 1 0
2 3 1 0
3 4 1 0
4 5 2 0
5 6 1 0
7 8 2 0
8 9 1 0
9 12 2 0
11 10 2 0
10 7 1 0
4 7 1 0
11 12 1 0
12 13 1 0
13 14 2 0
14 15 1 0
15 11 1 0
15 16 1 0
16 17 1 1
16 18 1 0
18 19 2 0
19 20 1 0
20 21 2 0
21 22 1 0
22 23 2 0
23 18 1 0
21 24 1 0
19 25 1 0
1 26 1 1
2 27 1 1
26 28 1 0
28 29 1 0
29 30 1 0
30 31 1 0
31 26 1 0
28 32 1 1
33 34 3 0
13 33 1 0
32 35 1 0
32 36 1 0
32 37 1 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 539.51Molecular Weight (Monoisotopic): 538.2015AlogP: 6.03#Rotatable Bonds: 5Polar Surface Area: 90.86Molecular Species: BASEHBA: 7HBD: 1#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 2CX Acidic pKa: ┄CX Basic pKa: 10.79CX LogP: 5.72CX LogD: 2.58Aromatic Rings: 3Heavy Atoms: 37QED Weighted: 0.43Np Likeness Score: -0.49
References 1. Jackson JJ, Ketcham JM, Younai A, Abraham B, Biannic B, Beck HP, Bui MHT, Chian D, Cutler G, Diokno R, Hu DX, Jacobson S, Karbarz E, Kassner PD, Marshall L, McKinnell J, Meleza C, Okal A, Pookot D, Reilly MK, Robles O, Shunatona HP, Talay O, Walker JR, Wadsworth A, Wustrow DJ, Zibinsky M.. (2019) Discovery of a Potent and Selective CCR4 Antagonist That Inhibits Treg Trafficking into the Tumor Microenvironment., 62 (13): [PMID:31259550 ] [10.1021/acs.jmedchem.9b00506 ]