The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.
docetaxel analogue ID: ALA352335
PubChem CID: 44379391
Max Phase: Preclinical
Molecular Formula: C44H55NO15
Molecular Weight: 837.92
Molecule Type: Small molecule
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: CC(=O)O[C@@]12CO[C@@H]1C[C@H](O)[C@@]1(C)C(=O)[C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)c4ccc(CO)cc4)C[C@@](O)([C@@H](OC(=O)c4ccccc4)[C@H]21)C3(C)C
Standard InChI: InChI=1S/C44H55NO15/c1-22-27(57-38(53)33(50)31(45-39(54)60-40(3,4)5)25-16-14-24(20-46)15-17-25)19-44(55)36(58-37(52)26-12-10-9-11-13-26)34-42(8,35(51)32(49)30(22)41(44,6)7)28(48)18-29-43(34,21-56-29)59-23(2)47/h9-17,27-29,31-34,36,46,48-50,55H,18-21H2,1-8H3,(H,45,54)/t27-,28-,29+,31-,32+,33+,34-,36-,42+,43-,44+/m0/s1
Standard InChI Key: SLGPLDVTHVMPBN-BGKJQISDSA-N
Molfile:
RDKit 2D
62 67 0 0 1 0 0 0 0 0999 V2000
9.1982 -4.2212 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.9122 -5.4530 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.3694 -5.7744 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.1982 -5.0479 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.3694 -4.3507 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7828 -5.0647 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.6178 -3.6367 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.5802 -5.8621 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7911 -3.6367 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5510 -4.3465 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5510 -5.7744 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.1419 -5.0605 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.7097 -5.0647 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.9122 -3.7996 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9958 -5.4780 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.6262 -5.0479 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.6095 -7.0813 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.2735 -5.0647 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5470 -3.8246 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0584 -7.6951 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.4279 -5.4780 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
10.3130 -6.1670 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.6262 -4.2212 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.6951 -6.2504 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
11.0270 -5.7619 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.2735 -4.2380 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
10.1001 -6.9644 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.9310 -2.8684 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.5595 -5.4780 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5428 -2.9979 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.7097 -4.2380 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.8413 -4.2505 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
7.2442 -7.5323 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
6.9519 -6.4884 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.3214 -8.4842 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.9268 -6.9644 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1.8205 -2.5971 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.3694 -2.9185 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
9.1982 -3.3945 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5595 -6.3005 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.8455 -5.0647 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.9874 -6.3047 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
9.9080 -2.9728 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.6095 -5.0647 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.1919 -4.3465 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.1377 -3.6242 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1399 -5.4780 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.8455 -6.7056 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1399 -6.2922 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4176 -7.5323 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
9.6867 -7.6784 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4176 -6.7056 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.1231 -8.6429 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7703 -9.0980 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1065 -2.1837 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.8163 -1.7704 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1065 -3.0104 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.3861 -9.4237 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.0291 -9.8829 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.8433 -10.0458 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.1982 -5.8747 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
11.4243 -4.8392 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
2 4 1 0
3 8 1 0
4 1 1 0
5 9 1 0
6 5 1 0
7 1 1 0
8 4 1 0
9 7 1 0
10 5 2 0
11 3 1 0
12 10 1 0
13 21 1 0
14 1 1 0
15 13 1 0
16 23 1 0
8 17 1 6
18 15 1 0
19 26 1 0
20 17 1 0
12 21 1 6
2 22 1 0
23 14 1 0
2 24 1 6
16 25 1 0
18 26 1 6
27 24 1 0
28 7 2 0
29 18 1 0
30 19 1 0
31 13 2 0
32 19 2 0
33 20 2 0
3 34 1 1
35 20 1 0
36 27 2 0
37 30 1 0
9 38 1 1
1 39 1 1
40 29 2 0
41 29 1 0
15 42 1 6
14 43 1 1
6 44 1 0
6 45 1 0
46 10 1 0
47 41 2 0
48 40 1 0
49 47 1 0
50 52 1 0
51 27 1 0
52 49 1 0
53 35 1 0
54 35 2 0
55 37 1 0
56 37 1 0
57 37 1 0
58 53 2 0
59 54 1 0
60 59 2 0
4 61 1 6
2 16 1 0
22 25 1 0
3 6 1 0
12 11 1 0
58 60 1 0
48 49 2 0
16 62 1 6
M END Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: 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: 837.92Molecular Weight (Monoisotopic): 837.3572AlogP: 2.75#Rotatable Bonds: 9Polar Surface Area: 244.68Molecular Species: NEUTRALHBA: 15HBD: 6#RO5 Violations: 3HBA (Lipinski): 16HBD (Lipinski): 6#RO5 Violations (Lipinski): 3CX Acidic pKa: 11.90CX Basic pKa: ┄CX LogP: 2.15CX LogD: 2.15Aromatic Rings: 2Heavy Atoms: 60QED Weighted: 0.12Np Likeness Score: 1.88
References 1. Bourzat J, Lavelle F, Commercon A. (1995) Synthesis and biological activity of Para-substituted 3-phenyl docetaxel analogs, 5 (8): [10.1016/0960-894X(95)00118-D ] 2. Sivakumar PM, Naga Vignesh, Ramesh Kumar G, Doble M. (2012) Computational approaches to enhance activity of taxanes as antimitotic agent, 21 (9): [10.1007/s00044-011-9779-x ]