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Pyrrospirone G ID: ALA4743394
PubChem CID: 139590338
Max Phase: Preclinical
Molecular Formula: C32H39NO5
Molecular Weight: 517.67
Molecule Type: Unknown
Associated Items:
Names and Identifiers Canonical SMILES: CC1=C[C@]2(C)C(=O)C[C@]34C[C@](O)(Cc5ccc(cc5)O[C@H]5[C@@H]([C@@H]1[C@]1(C)C[C@H](C)C[C@H](C)[C@@H]51)[C@H]2C3=O)NC4=O
Standard InChI: InChI=1S/C32H39NO5/c1-16-10-17(2)24-26-22-23(30(24,5)11-16)18(3)12-29(4)21(34)14-31(27(35)25(22)29)15-32(37,33-28(31)36)13-19-6-8-20(38-26)9-7-19/h6-9,12,16-17,22-26,37H,10-11,13-15H2,1-5H3,(H,33,36)/t16-,17+,22+,23-,24+,25+,26+,29-,30+,31+,32-/m1/s1
Standard InChI Key: DJXHULBSNKVOCR-DDIFOEQUSA-N
Molfile:
RDKit 2D
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10.2332 -14.9814 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.2087 -14.1591 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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10.7626 -12.0558 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.5480 -12.8441 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.2314 -13.2919 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.8684 -12.7803 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
11.5786 -12.0164 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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9.8148 -10.7289 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.1972 -12.2302 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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7.4046 -12.8091 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
11.1026 -11.3048 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.9617 -9.8853 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
8.0295 -9.4793 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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8.8831 -12.3572 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
6.6977 -12.3923 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.5204 -10.1542 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.6703 -11.5613 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.6242 -10.6386 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.7731 -10.1812 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
9.3341 -10.0642 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.4797 -12.2914 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0
5.9831 -11.9843 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6982 -13.2215 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.1896 -10.3522 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
10.2256 -10.0057 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2646 -10.7449 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
12.0264 -11.3329 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
11.0445 -14.7136 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
11.9359 -13.6983 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
1 2 2 0
2 3 1 0
3 4 2 0
4 5 1 0
5 6 2 0
6 1 1 0
7 8 1 0
8 9 1 0
9 10 1 0
10 11 1 0
7 11 1 1
29 25 1 0
15 39 1 1
15 26 1 0
18 30 1 0
16 22 1 1
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28 36 1 1
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35 28 1 0
30 27 1 6
20 32 1 1
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18 12 1 6
31 24 2 0
14 34 1 1
19 26 1 0
13 21 2 0
30 14 1 0
15 35 1 0
7 23 1 0
17 31 1 0
23 31 1 0
17 38 1 1
17 33 1 0
17 14 1 0
20 30 1 0
28 16 1 0
14 13 1 0
13 7 1 0
20 29 1 0
20 19 1 0
11 40 2 0
41 9 1 0
9 42 1 6
1 12 1 0
4 41 1 0
M END Associated Targets(Human) Molecule Features Natural Product: YesOral: 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: 517.67Molecular Weight (Monoisotopic): 517.2828AlogP: 4.24#Rotatable Bonds: ┄Polar Surface Area: 92.70Molecular Species: NEUTRALHBA: 5HBD: 2#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 1CX Acidic pKa: 10.62CX Basic pKa: ┄CX LogP: 4.48CX LogD: 4.48Aromatic Rings: 1Heavy Atoms: 38QED Weighted: 0.40Np Likeness Score: 2.01
References 1. Ge H,Shi M,Ma M,Lian XY,Zhang Z. (2021) Evaluation of the antiproliferative activity of 106 marine microbial metabolites against human lung cancer cells and potential antiproliferative mechanism of purpuride G., 39 [PMID:33691166 ] [10.1016/j.bmcl.2021.127915 ]