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Helioscopid E ID: ALA5194754
PubChem CID: 168284697
Max Phase: Preclinical
Molecular Formula: C31H40O9
Molecular Weight: 556.65
Associated Items:
Names and Identifiers Canonical SMILES: CC(=O)O[C@@H]1C[C@@H](O)/C(C)=C/[C@H]2[C@@H](OC(=O)c3ccccc3)[C@@H](C)C[C@]2(OC(C)=O)C(=O)/C(C)=C/[C@H](O)C1(C)C
Standard InChI: InChI=1S/C31H40O9/c1-17-13-23-27(39-29(37)22-11-9-8-10-12-22)19(3)16-31(23,40-21(5)33)28(36)18(2)14-25(35)30(6,7)26(15-24(17)34)38-20(4)32/h8-14,19,23-27,34-35H,15-16H2,1-7H3/b17-13+,18-14+/t19-,23-,24+,25-,26+,27-,31+/m0/s1
Standard InChI Key: TXHMUROLBIZPHN-WQRPIHSESA-N
Molfile:
RDKit 2D
41 43 0 0 0 0 0 0 0 0999 V2000
-1.0016 2.8513 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.7106 2.0793 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.1111 2.0066 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.5332 2.7153 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.5665 1.3187 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3385 1.6096 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4113 2.4314 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
2.0473 1.1875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1591 0.3701 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9442 0.1163 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.1168 -0.6904 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5045 -1.2431 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
3.9018 -0.9442 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.5899 -0.2269 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.7682 -0.1540 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.3459 -0.8629 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
0.3127 0.5336 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2736 1.3508 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.4592 0.2427 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.1680 0.6649 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.2799 1.4823 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.0919 1.6284 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.4817 0.9014 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.9108 0.3059 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.0569 -0.5060 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.8333 -0.7854 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.9794 -1.5973 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.3493 -2.1298 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.4955 -2.9418 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.2717 -3.2212 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.9018 -2.6886 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.7556 -1.8767 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.4633 -0.2528 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.2992 0.7895 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.5359 2.2665 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.3431 2.4369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.5992 3.2212 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.8943 1.8231 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.2038 -0.1592 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
2.8740 1.1875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.4615 1.9021 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2 1 2 0
3 2 1 0
3 4 1 0
3 5 2 0
5 6 1 0
6 7 1 6
6 8 1 0
8 9 1 0
9 10 1 6
10 11 1 0
11 12 2 0
11 13 1 0
14 9 1 0
15 14 1 0
15 16 1 1
17 15 1 0
17 18 1 0
19 17 2 0
20 19 1 0
21 2 1 0
20 21 1 0
21 22 1 0
22 23 1 0
24 23 1 0
20 24 1 0
24 25 1 1
25 26 1 0
26 27 1 0
28 27 2 0
29 28 1 0
30 29 2 0
31 30 1 0
27 32 1 0
32 31 2 0
26 33 2 0
23 34 1 1
21 35 1 1
35 36 1 0
36 37 2 0
36 38 1 0
20 39 1 6
8 40 1 0
8 41 1 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Topical: 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: 556.65Molecular Weight (Monoisotopic): 556.2672AlogP: 3.72#Rotatable Bonds: 4Polar Surface Area: 136.43Molecular Species: NEUTRALHBA: 9HBD: 2#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: ┄CX LogP: 3.79CX LogD: 3.79Aromatic Rings: 1Heavy Atoms: 40QED Weighted: 0.32Np Likeness Score: 2.38
References 1. Zhou CG, Xiang ZN, Zhao N, Sun X, Hu ZF, Wu JL, Xia RF, Chen C, Su JC, Chen JC, Wan LS.. (2022) Jatrophane Diterpenoids with Kv1.3 Ion Channel Inhibitory Effects from Euphorbia helioscopia ., 85 (4.0): [PMID:35245067 ] [10.1021/acs.jnatprod.1c00879 ]