ID: ALA5281097

Max Phase: Preclinical

Molecular Formula: C70H87ClFN7O21

Molecular Weight: 1416.94

Associated Items:

This compound is not in our inventory system

Names and Identifiers

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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M  END

Alternative Forms

  1. Parent:

    ALA5281097

    ---

Associated Targets(non-human)

4T1 (1737 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 1416.94Molecular Weight (Monoisotopic): 1415.5628AlogP: #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:

References

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