Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Comploside II
ID: ALA5267673
Max Phase: Preclinical
Molecular Formula: C54H88O23
Molecular Weight: 1105.28
Associated Items:
ID: ALA5267673
Max Phase: Preclinical
Molecular Formula: C54H88O23
Molecular Weight: 1105.28
Associated Items:
Canonical SMILES: C[C@@H]1O[C@@H](O[C@H]2[C@H](O[C@H]3[C@H](O[C@H]4CC[C@@]5(C)[C@@H](CC[C@]6(C)[C@@H]5CC=C5[C@@H]7CC(C)(C)C[C@@H](O[C@@H]8O[C@H](CO)[C@@H](O)[C@H](O)[C@H]8O)[C@]7(C)CC[C@]56C)[C@@]4(C)CO)O[C@H](C(=O)O)[C@@H](O)[C@@H]3O)O[C@H](CO)[C@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O
Standard InChI: InChI=1S/C54H88O23/c1-22-31(58)34(61)39(66)45(70-22)76-42-36(63)33(60)26(20-56)72-47(42)77-43-38(65)37(64)41(44(68)69)75-48(43)73-29-12-13-51(5)27(52(29,6)21-57)11-14-54(8)28(51)10-9-23-24-17-49(2,3)18-30(50(24,4)15-16-53(23,54)7)74-46-40(67)35(62)32(59)25(19-55)71-46/h9,22,24-43,45-48,55-67H,10-21H2,1-8H3,(H,68,69)/t22-,24-,25+,26+,27+,28+,29-,30+,31-,32+,33-,34+,35-,36-,37-,38-,39+,40+,41-,42+,43+,45-,46-,47-,48+,50+,51-,52+,53+,54+/m0/s1
Standard InChI Key: VQTMNYUOKHAJED-RULIEQGVSA-N
Molfile:
RDKit 2D 84 92 0 0 0 0 0 0 0 0999 V2000 -3.5890 -5.3077 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.5890 -4.4827 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.8740 -4.0702 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1590 -4.4827 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.8740 -3.2451 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1590 -2.8326 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.5890 -2.8326 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0054 -2.2489 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5890 -2.0076 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.3041 -1.5950 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.3041 -0.7700 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.5892 -1.1827 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -3.5890 -0.3575 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.5890 0.4675 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.8740 0.8800 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.1591 1.2927 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -2.1590 0.4675 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.4440 0.8800 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.7289 0.4675 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3164 -0.2475 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5086 -0.2475 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -1.1414 -0.2475 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0139 0.8800 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.7288 1.2927 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 0.7010 0.4675 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4161 0.8800 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4161 1.7050 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4161 2.5300 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1311 2.1175 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1311 1.2925 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8461 1.7050 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5611 2.1175 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5611 2.9425 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2762 2.5300 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2762 3.3551 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.9915 2.9425 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.9915 2.1170 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7067 1.7045 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7067 0.8791 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.9920 0.4661 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2770 0.8786 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2770 1.7040 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.5620 0.4658 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5620 -0.3595 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.9920 -0.3593 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.4217 0.4663 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.4214 2.1173 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.7064 2.5298 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 4.2762 4.1801 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5611 4.5926 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9736 5.3077 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1486 5.3077 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8461 4.1801 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8461 3.3551 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1312 3.7678 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.1311 2.9425 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4161 3.3551 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7010 2.9425 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7010 2.1175 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7010 1.2920 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 -0.0139 1.7050 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0139 2.5300 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.7289 2.1175 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4440 1.7050 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.8740 1.7050 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.5890 2.1175 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.5890 2.9425 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.3041 3.3551 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -2.8740 3.3551 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.3041 1.7050 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0191 2.1175 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.3041 0.8800 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0191 0.4675 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.0191 -0.3575 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.7341 -0.7700 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.4217 -0.3575 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.4217 0.4675 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.7341 -1.5950 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.4217 -2.0076 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.0191 -2.0076 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0191 -2.8326 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.3041 -3.2451 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.3041 -4.0702 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.0191 -4.4827 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2 1 1 1 2 3 1 0 3 4 1 6 3 5 1 0 5 6 1 6 5 7 1 0 7 8 1 6 7 9 1 0 10 9 1 6 10 11 1 0 11 12 1 6 11 13 1 0 14 13 1 6 14 15 1 0 15 16 1 6 15 17 1 0 18 17 1 1 18 19 1 0 19 20 1 1 20 21 1 0 19 22 1 0 23 19 1 0 23 24 1 6 23 25 1 0 25 26 1 0 26 27 1 0 27 28 1 1 27 29 1 0 29 30 1 6 29 31 1 0 31 32 1 0 32 33 1 0 33 34 1 1 33 35 1 0 35 36 1 1 36 37 1 0 38 37 1 0 39 38 1 0 40 39 1 0 41 40 1 0 42 41 1 0 37 42 1 0 41 43 1 1 43 44 1 0 40 45 1 6 39 46 1 1 38 47 1 6 37 48 1 6 49 35 1 0 50 49 1 0 50 51 1 0 50 52 1 0 53 50 1 0 54 53 1 0 33 54 1 0 54 55 1 1 56 54 1 0 56 29 1 0 57 56 2 0 58 57 1 0 59 58 1 0 27 59 1 0 59 60 1 6 61 59 1 0 61 23 1 0 61 62 1 1 63 61 1 0 64 63 1 0 18 64 1 0 65 15 1 0 66 65 1 0 66 67 1 1 67 68 1 0 67 69 2 0 70 66 1 0 70 71 1 6 72 70 1 0 14 72 1 0 72 73 1 1 74 11 1 0 75 74 1 0 75 76 1 1 76 77 1 0 78 75 1 0 78 79 1 1 80 78 1 0 10 80 1 0 80 81 1 1 7 82 1 0 83 82 1 0 83 2 1 0 83 84 1 6 M END
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Natural Product: Yes | 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 |
---|
Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
---|
Molecular Weight: 1105.28 | Molecular Weight (Monoisotopic): 1104.5716 | 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. Xu GB, Xiao YH, Zhang QY, Zhou M, Liao SG.. (2018) Hepatoprotective natural triterpenoids., 145 [PMID:29353722] [10.1016/j.ejmech.2018.01.011] |
Source(1):