SB-T-1212

ID: ALA339531

PubChem CID: 9940743

Max Phase: Preclinical

Molecular Formula: C43H57NO15

Molecular Weight: 827.92

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Synonyms: SB-T-1212 | SB-T-1212|CHEMBL339531|SCHEMBL12168467

Canonical SMILES:  CC(=O)O[C@H]1C(=O)[C@@]2(C)[C@H]([C@H](OC(=O)c3ccccc3)[C@]3(O)C[C@H](OC(=O)[C@H](O)[C@H](C=C(C)C)NC(=O)OC(C)(C)C)C(C)=C1C3(C)C)[C@]1(OC(C)=O)CO[C@@H]1C[C@@H]2O

Standard InChI:  InChI=1S/C43H57NO15/c1-21(2)17-26(44-38(52)59-39(6,7)8)31(48)37(51)56-27-19-43(53)35(57-36(50)25-15-13-12-14-16-25)33-41(11,28(47)18-29-42(33,20-54-29)58-24(5)46)34(49)32(55-23(4)45)30(22(27)3)40(43,9)10/h12-17,26-29,31-33,35,47-48,53H,18-20H2,1-11H3,(H,44,52)/t26-,27-,28-,29+,31+,32+,33-,35-,41+,42-,43+/m0/s1

Standard InChI Key:  NRISGROGJFACOP-LYEXFJIESA-N

Molfile:  

     RDKit          2D

 61 65  0  0  1  0  0  0  0  0999 V2000
    9.0000   -2.4917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0125   -3.5042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0125   -4.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2125   -3.2917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1542   -3.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9167   -3.4042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3625   -2.1542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8042   -4.0042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5625   -2.3667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5000   -3.5792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3542   -4.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6000   -4.3917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5792   -1.9042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2167   -4.7542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5917   -2.9167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0167   -4.8042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6292   -5.3292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8292   -5.1167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8292   -4.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6000   -5.5167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0125   -4.9792    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8042   -3.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3792   -2.1167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2250   -4.2917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3875   -3.1292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6250   -4.3167    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2417   -5.6917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1500   -1.6542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0167   -4.5042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3250   -1.6542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4500   -1.3292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2417   -4.6792    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0042   -3.9542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6167   -3.2917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8875   -5.9292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4500   -6.4917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9542   -5.0542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0042   -6.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2292   -5.3042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9125   -2.3667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4417   -4.4542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9917   -1.6667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7875   -1.1042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8292   -6.1292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5792   -2.9167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4125   -4.0542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7417   -3.2542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9042   -0.9417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6042   -3.9292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8625   -7.0667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2417   -6.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8292   -6.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5917   -6.9417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4375   -3.6292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8542   -5.0417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6417   -4.2417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0000   -7.6542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2417   -6.9417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8250   -7.6667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4250   -4.0917    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1751   -2.3333    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  4  1  0
  3  8  1  0
  4  1  1  0
  5  9  1  0
  6  5  1  0
  7  1  1  0
  8  4  1  0
  9  7  1  0
 10  5  2  0
 11  3  1  0
 12 10  1  0
 13  1  1  0
 14 21  1  0
 15 23  1  0
  8 16  1  6
 17 14  1  0
 18 17  1  0
 19 26  1  0
 20 16  1  0
 12 21  1  6
  2 22  1  0
 23 13  1  0
  2 24  1  6
 15 25  1  0
 18 26  1  6
 27 18  1  0
  9 28  1  1
 29 24  1  0
 30 28  1  0
 31  7  2  0
 32 19  1  0
 33 14  2  0
 34 19  2  0
 35 20  2  0
 36 27  2  0
  3 37  1  1
 38 20  1  0
 39 29  2  0
 40 30  2  0
 41 32  1  0
  1 42  1  1
 13 43  1  1
 17 44  1  6
  6 45  1  0
  6 46  1  0
 47 10  1  0
 48 30  1  0
 49 29  1  0
 50 36  1  0
 51 36  1  0
 52 38  1  0
 53 38  2  0
 54 41  1  0
 55 41  1  0
 56 41  1  0
 57 53  1  0
 58 52  2  0
 59 57  2  0
  4 60  1  6
  2 15  1  0
 22 25  1  0
  3  6  1  0
 11 12  1  0
 58 59  1  0
 15 61  1  6
M  END

Associated Targets(Human)

A121 (119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A2780 (11979 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7R (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 827.92Molecular Weight (Monoisotopic): 827.3728AlogP: 3.42#Rotatable Bonds: 9
Polar Surface Area: 230.52Molecular Species: NEUTRALHBA: 15HBD: 4
#RO5 Violations: 2HBA (Lipinski): 16HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.95CX Basic pKa: CX LogP: 2.99CX LogD: 2.99
Aromatic Rings: 1Heavy Atoms: 59QED Weighted: 0.16Np Likeness Score: 2.13

References

1. Ojima I, Duclos O, Kuduk SD, Sun C, Slater JC, Lavelle F, Veith JM, Bernacki RJ.  (1994)  Synthesis and biological activity of 3-alkyl- and 3-alkenyl-3-dephenyldocetaxels,  (21): [10.1016/S0960-894X(01)80298-5]
2. Ojima I, Kuduk SD, Pera P, Veith JM, Bernacki RJ..  (1997)  Synthesis and structure-activity relationships of nonaromatic taxoids: effects of alkyl and alkenyl ester groups on cytotoxicity.,  40  (3): [PMID:9022794] [10.1021/jm9606711]
3. Ojima I, Slater JC, Michaud E, Kuduk SD, Bounaud PY, Vrignaud P, Bissery MC, Veith JM, Pera P, Bernacki RJ..  (1996)  Syntheses and structure-activity relationships of the second-generation antitumor taxoids: exceptional activity against drug-resistant cancer cells.,  39  (20): [PMID:8831755] [10.1021/jm9604080]

Source