Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5281097
Max Phase: Preclinical
Molecular Formula: C70H87ClFN7O21
Molecular Weight: 1416.94
Associated Items:
ID: ALA5281097
Max Phase: Preclinical
Molecular Formula: C70H87ClFN7O21
Molecular Weight: 1416.94
Associated Items:
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](OC(=O)CCC(=O)NCCCC[C@H](NC(=O)CC[C@@H](NC(=O)[C@H](C)NC(=O)/C=C/c4ccc(F)cc4Cl)C(N)=O)C(N)=O)[C@@H](NC(=O)OC(C)(C)C)c4ccccc4)C[C@@](O)([C@@H](OC(=O)c4ccccc4)[C@H]21)C3(C)C
Standard InChI: InChI=1S/C70H87ClFN7O21/c1-36-46(34-70(94)59(98-63(91)41-20-14-11-15-21-41)57-68(9,58(87)55(86)53(36)67(70,7)8)47(81)33-48-69(57,35-95-48)99-38(3)80)96-64(92)56(54(40-18-12-10-13-19-40)79-65(93)100-66(4,5)6)97-52(85)30-29-49(82)75-31-17-16-22-44(60(73)88)77-51(84)28-26-45(61(74)89)78-62(90)37(2)76-50(83)27-24-39-23-25-42(72)32-43(39)71/h10-15,18-21,23-25,27,32,37,44-48,54-57,59,81,86,94H,16-17,22,26,28-31,33-35H2,1-9H3,(H2,73,88)(H2,74,89)(H,75,82)(H,76,83)(H,77,84)(H,78,90)(H,79,93)/b27-24+/t37-,44-,45+,46-,47-,48+,54-,55+,56+,57-,59-,68+,69-,70+/m0/s1
Standard InChI Key: BSNLJQZNHGRNQV-VALSQYGOSA-N
Molfile:
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0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.0136 -15.8717 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.0011 -16.6888 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.7275 -15.4740 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.7025 -17.1082 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.6900 -17.9253 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.3913 -18.3447 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 8.9761 -18.3230 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.3788 -19.1618 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.0802 -19.5811 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.0677 -20.3982 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.7691 -20.8176 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.7566 -21.6347 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.4579 -22.0541 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.4454 -22.8712 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 13.1718 -21.6564 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 11.0427 -22.0324 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 10.3413 -21.6131 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.6274 -22.0108 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.3538 -20.7960 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.9261 -21.5914 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.2122 -21.9891 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.5108 -21.5697 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 8.1997 -22.8062 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.4858 -23.2039 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.9011 -23.2256 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 6.7969 -21.9674 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.0956 -21.5481 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.7844 -22.7845 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.1081 -20.7310 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.3817 -21.9458 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 4.6803 -21.5264 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9664 -21.9241 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6928 -20.7093 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.2651 -21.5047 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5512 -21.9025 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8535 -21.4814 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1401 -21.8785 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1271 -22.6964 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8335 -23.1157 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.5440 -22.7163 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.2475 -23.1320 0.0000 Cl 0 0 0 0 0 0 0 0 0 0 0 0 0.4138 -23.0951 0.0000 F 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 22 1 0 14 1 1 0 15 13 1 0 16 24 1 0 19 17 1 6 8 18 1 6 19 15 1 0 20 17 1 0 21 18 1 0 12 22 1 6 23 2 1 0 24 14 1 0 2 25 1 6 26 16 1 0 9 27 1 1 28 25 1 0 29 7 2 0 30 13 2 0 31 20 2 0 32 21 2 0 3 33 1 1 34 20 1 0 35 21 1 0 36 19 1 0 37 28 2 0 1 38 1 1 15 39 1 6 14 40 1 1 41 6 1 0 42 6 1 0 43 10 1 0 44 28 1 0 45 35 1 0 46 35 2 0 47 36 2 0 48 36 1 0 49 48 2 0 50 45 2 0 51 46 1 0 52 47 1 0 53 49 1 0 54 51 2 0 4 55 1 6 16 56 1 6 16 2 1 0 23 26 1 0 3 6 1 0 11 12 1 0 54 50 1 0 52 53 2 0 34 57 1 0 57 58 1 0 57 59 1 0 57 60 1 0 39 61 1 0 61 62 1 0 61 63 2 0 62 64 1 0 64 65 1 0 65 66 1 0 65 67 2 0 66 68 1 0 68 69 1 0 69 70 1 0 70 71 1 0 72 71 1 1 72 73 1 0 73 74 1 0 73 75 2 0 72 76 1 0 76 77 1 0 77 78 1 0 77 79 2 0 78 80 1 0 80 81 1 0 81 82 1 0 81 83 1 6 83 84 2 0 83 85 1 0 82 86 1 0 86 87 1 0 86 88 2 0 87 89 1 1 87 90 1 0 90 91 1 0 91 92 1 0 91 93 2 0 92 94 2 0 94 95 1 0 95 96 2 0 96 97 1 0 97 98 2 0 98 99 1 0 99100 2 0 100 95 1 0 100101 1 0 98102 1 0 M END
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: | Topical: No | First In Class: No | Black Box: No |
Chirality: No | Availability: No | Prodrug: No |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 1416.94 | Molecular Weight (Monoisotopic): 1415.5628 | AlogP: ┄ | #Rotatable Bonds: ┄ |
Polar Surface Area: ┄ | Molecular Species: ┄ | HBA: ┄ | HBD: ┄ |
#RO5 Violations: ┄ | HBA (Lipinski): ┄ | HBD (Lipinski): ┄ | #RO5 Violations (Lipinski): ┄ |
CX Acidic pKa: ┄ | CX Basic pKa: ┄ | CX LogP: ┄ | CX LogD: ┄ |
Aromatic Rings: ┄ | Heavy Atoms: ┄ | QED Weighted: ┄ | Np Likeness Score: ┄ |
1. Wen X, Zheng P, Ma Y, Ou Y, Huang W, Li S, Liu S, Zhang X, Wang Z, Zhang Q, Cheng W, Lin R, Li H, Cai Y, Hu C, Wu N, Wan L, Pan T, Rao J, Bei X, Wu W, Jin J, Yan J, Liu G.. (2018) Salutaxel, a Conjugate of Docetaxel and a Muramyl Dipeptide (MDP) Analogue, Acts as Multifunctional Prodrug That Inhibits Tumor Growth and Metastasis., 61 (4): [PMID:29357251] [10.1021/acs.jmedchem.7b01407] |
Source(1):