General
Preferred name
TALTOBULIN
Synonyms
HTI 286 ()
Taltobulin (hydrochloride) ()
HTI-286 ()
SPA-110 ()
HTI-286 hydrochloride ()
SPA-110 hydrochloride ()
Taltobulin trifluoroacetate ()
Taltobulin (trifluoroacetate) ()
Taltobulina ()
Taltobuline ()
P&D ID
PD016647
CAS
228266-40-8
228266-41-9
Tags
available
drug candidate
nuisance
Drug indication
Solid tumour/cancer
Drug Status
investigational
Max Phase
2.0
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION
Taltobulin (HTI-286), a synthetic analogue of the tripeptide hemiasterlin, is a potent antimicrotubule agent that circumvents P-glycoprotein-mediated resistance in vitro and in vivo. Taltobulin inhibits the polymerization of purified tubulin, disrupts microtubule organization in cells, and induces mitotic arrest, as well as apoptosis[1].
DESCRIPTION
Taltobulin hydrochloride (HTI-286 hydrochloride), a synthetic analogue of the tripeptide hemiasterlin, is a potent antimicrotubule agent that circumvents P-glycoprotein-mediated resistance in vitro and in vivo. Taltobulin hydrochloride inhibits the polymerization of purified tubulin, disrupts microtubule organization in cells, and induces mitotic arrest, as well as apoptosis[1].
DESCRIPTION
Taltobulin, also known as HTI-286 and SPA-110, is a fully synthetic analog of the natural tripeptide hemiasterlin, inhibits tubulin polymerization and circumvents transport-based resistance to taxanes. HTI-286 was a potent inhibitor of proliferation (mean IC50 = 2.5 ± 2.1 nm in 18 human tumor cell lines) and had substantially less interaction with multidrug resistance protein (P-glycoprotein) than currently used antimicrotubule agents, including paclitaxel, docetaxel, vinorelbine, or vinblastine.
(BOC Sciences Bioactive Compounds)
DESCRIPTION
Taltobulin trifluoroacetate is a potent antimicrotubule agent that circumvents P-glycoprotein-mediated resistance in vitro and in vivo. Taltobulin trifluoroacetate inhibits the polymerization of purified tubulin, disrupts microtubule organization in cells, and induces mitotic arrest, as well as apoptosis.
(BOC Sciences Bioactive Compounds)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Cell lines
7
Organisms
0
Compound Sets
11
Axon Medchem Screening Library
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
ChEMBL Drugs
CZ-OPENSCREEN Bioactive Library
Drug Repurposing Hub
DrugMAP
EU-OPENSCREEN Bioactive Compound Library
Nuisance compounds in cellular assays
ReFrame library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
34
Molecular Weight
473.33
Hydrogen Bond Acceptors
4
Hydrogen Bond Donors
3
Rotatable Bonds
10
Ring Count
1
Aromatic Ring Count
1
cLogP
3.6
TPSA
98.74
Fraction CSP3
0.59
Chiral centers
3.0
Largest ring
6.0
QED
0.45
Structural alerts
1
Tubulin modulation
Nuisance compounds
Custom attributes
(extracted from source data)
MOA
tubulin polymerization inhibitor
Target
Tubulin inhibitor
ADC Payload
Apoptosis
Microtubule/Tubulin
ADC Cytotoxin
Pathway
Antibody-drug Conjugate/ADC Related
Cell Cycle/DNA Damage
cytoskeleton
Solubility
Soluble in DMSO, not in water
Source data

