ID: ALA4170662

Max Phase: Preclinical

Molecular Formula: C74H104N20O18S2

Molecular Weight: 1625.90

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](CO)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@@H]2CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(=O)O)C(=O)NCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N2

Standard InChI:  InChI=1S/C74H104N20O18S2/c1-4-39(2)58-68(108)89-51-37-113-114-38-52(88-61(101)45(19-10-26-79-73(75)76)82-56(97)35-81-60(100)47(34-57(98)99)84-66(106)53-21-12-28-92(53)70(110)48(86-64(51)104)32-41-15-6-5-7-16-41)65(105)91-59(40(3)96)69(109)83-46(20-11-27-80-74(77)78)62(102)87-50(36-95)63(103)85-49(33-42-24-25-43-17-8-9-18-44(43)31-42)71(111)94-30-14-23-55(94)72(112)93-29-13-22-54(93)67(107)90-58/h5-9,15-18,24-25,31,39-40,45-55,58-59,95-96H,4,10-14,19-23,26-30,32-38H2,1-3H3,(H,81,100)(H,82,97)(H,83,109)(H,84,106)(H,85,103)(H,86,104)(H,87,102)(H,88,101)(H,89,108)(H,90,107)(H,91,105)(H,98,99)(H4,75,76,79)(H4,77,78,80)/t39-,40+,45-,46-,47-,48-,49-,50-,51-,52-,53-,54-,55-,58-,59-/m0/s1

Standard InChI Key:  DRMCRYSYJGXXTH-LEBNSUCRSA-N

Associated Targets(Human)

Trypsin III 45 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypsin I 2306 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Trypsin I 1205 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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

Properties

Molecular Weight: 1625.90Molecular Weight (Monoisotopic): 1624.7279AlogP: #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. de Veer SJ, Li CY, Swedberg JE, Schroeder CI, Craik DJ..  (2018)  Engineering potent mesotrypsin inhibitors based on the plant-derived cyclic peptide, sunflower trypsin inhibitor-1.,  155  [PMID:29936356] [10.1016/j.ejmech.2018.06.029]

Source