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(4R)-2-((S)-4-((Z)-2-(2-aminothiazol-4-yl)-2-(2-carboxypropan-2-yloxyimino)acetamido)-3-oxoisoxazolidin-2-yl)-4-(benzyloxycarbonylamino)-5-oxotetrahydrofuran-2-carboxylic acid ID: ALA3265222
PubChem CID: 90656114
Max Phase: Preclinical
Molecular Formula: C25H26N6O12S
Molecular Weight: 634.58
Molecule Type: Small molecule
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: CC(C)(O/N=C(\C(=O)N[C@H]1CON(C2(C(=O)O)C[C@@H](NC(=O)OCc3ccccc3)C(=O)O2)C1=O)c1csc(N)n1)C(=O)O
Standard InChI: InChI=1S/C25H26N6O12S/c1-24(2,20(35)36)43-30-16(15-11-44-22(26)28-15)17(32)27-14-10-41-31(18(14)33)25(21(37)38)8-13(19(34)42-25)29-23(39)40-9-12-6-4-3-5-7-12/h3-7,11,13-14H,8-10H2,1-2H3,(H2,26,28)(H,27,32)(H,29,39)(H,35,36)(H,37,38)/b30-16-/t13-,14+,25?/m1/s1
Standard InChI Key: MPMHBBHMNIUZMW-JRNNHGNASA-N
Molfile:
RDKit 2D
44 47 0 0 0 0 0 0 0 0999 V2000
30.4755 -1.1309 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.1853 -1.5395 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.1843 -0.7204 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.2178 -4.4203 0.0000 S 0 0 0 0 0 0 0 0 0 0 0 0
29.0350 -4.4203 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
29.2894 -3.6436 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
28.6264 -3.1615 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
27.9677 -3.6436 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
27.1904 -3.3914 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
30.0669 -3.3921 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
30.6735 -3.9398 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.4510 -3.6883 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
30.5025 -4.7389 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
30.2379 -2.5930 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
31.0155 -2.3416 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
32.0007 -1.4825 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.4608 -2.1599 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
32.3621 -0.7477 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
32.0575 -4.2360 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.9682 -5.0467 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.7143 -5.3802 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
33.2620 -4.7736 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
32.8543 -4.0654 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
31.2592 -5.4531 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
32.8852 -6.1794 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.3376 -6.7860 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
32.7452 -7.4942 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
33.5449 -7.3254 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
33.6313 -6.5128 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
32.4118 -8.2403 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
33.6732 -5.9738 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
34.2469 -6.5508 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
33.8891 -5.1854 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
34.1514 -7.8730 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
34.9290 -7.6215 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
35.5355 -8.1691 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
35.0999 -6.8224 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
35.3646 -8.9682 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
35.9712 -9.5158 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
35.7955 -10.3124 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
36.4013 -10.8598 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
37.1798 -10.6084 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
37.3491 -9.8046 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
36.7419 -9.2607 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2 1 1 0
3 2 1 0
4 5 1 0
5 6 2 0
6 7 1 0
7 8 2 0
8 4 1 0
8 9 1 0
6 10 1 0
10 11 1 0
11 12 1 0
11 13 2 0
10 14 2 0
14 15 1 0
15 2 1 0
2 16 1 0
16 17 1 0
16 18 2 0
19 12 1 1
19 20 1 0
20 21 1 0
21 22 1 0
22 23 1 0
23 19 1 0
20 24 2 0
25 26 1 0
26 27 1 0
27 28 1 0
28 29 1 0
29 25 1 0
21 25 1 0
27 30 2 0
25 31 1 0
31 32 1 0
31 33 2 0
28 34 1 1
34 35 1 0
35 36 1 0
35 37 2 0
36 38 1 0
38 39 1 0
39 40 2 0
40 41 1 0
41 42 2 0
42 43 1 0
43 44 2 0
44 39 1 0
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: 634.58Molecular Weight (Monoisotopic): 634.1329AlogP: -0.41#Rotatable Bonds: 11Polar Surface Area: 258.37Molecular Species: ACIDHBA: 14HBD: 5#RO5 Violations: 2HBA (Lipinski): 18HBD (Lipinski): 6#RO5 Violations (Lipinski): 3CX Acidic pKa: 2.24CX Basic pKa: 3.92CX LogP: 0.24CX LogD: -5.26Aromatic Rings: 2Heavy Atoms: 44QED Weighted: 0.12Np Likeness Score: 0.01
References 1. Starr J, Brown MF, Aschenbrenner L, Caspers N, Che Y, Gerstenberger BS, Huband M, Knafels JD, Lemmon MM, Li C, McCurdy SP, McElroy E, Rauckhorst MR, Tomaras AP, Young JA, Zaniewski RP, Shanmugasundaram V, Han S.. (2014) Siderophore receptor-mediated uptake of lactivicin analogues in gram-negative bacteria., 57 (9): [PMID:24694215 ] [10.1021/jm500219c ]