Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C37H72N4O5S.3ClH |
| Molecular Weight | 794.439 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 11 / 11 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.Cl.CC(C)[C@@H](CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@H]4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12C)NCCCNCCCCNCCCN)OS(O)(=O)=O
InChI
InChIKey=DJYRGAKPWPDNTA-YPRMBGODSA-N
InChI=1S/C37H72N4O5S.3ClH/c1-26(2)34(46-47(43,44)45)13-10-27(3)30-11-12-31-35-32(15-17-37(30,31)5)36(4)16-14-29(24-28(36)25-33(35)42)41-23-9-22-40-20-7-6-19-39-21-8-18-38;;;/h26-35,39-42H,6-25,38H2,1-5H3,(H,43,44,45);3*1H/t27-,28-,29+,30-,31+,32+,33-,34-,35+,36+,37-;;;/m1.../s1
| Molecular Formula | C37H72N4O5S |
| Molecular Weight | 685.056 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 11 / 11 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Trodusquemine (MSI-1436) is a "first-in-class" highly selective non-competitive, allosteric inhibitor of PTP1B that can cross the blood-brain barrier to suppress feeding and promote insulin sensitivity and glycemic control. Trodusquemine is a naturally occurring cholestane that can be purified from the liver of the dogfish shark, Squalus acanthias, but it can also be manufactured synthetically by a fairly laborious process that requires several weeks. Trodusquemine has potential hypoglycemic, anti-diabetic, anti-obesity, and antineoplastic activities. Upon administration, trodusquemine selectively targets and inhibits PTP1B, thereby preventing PTP1B-mediated signaling. This prevents the dephosphorylation of the insulin receptor, which improves insulin signaling and insulin sensitivity, and decreases blood glucose levels. In susceptible cancer cells, inhibition of PTP1B causes a reduction of tumor cell proliferation.
CNS Activity
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT00806338
Diabetes Mellitus; Obesity:
Trodusquemine 3 - 10 mg/m2.
A single dose of Trodusquemine will be administered every 72 hours on Days 0, 3, 6, 9, 12, 15, 18 and 21. Doses are 3mg/m2 in cohort 1, 6mg/m2 in cohort 2 and 10mg/m2 in cohort 3.
Route of Administration:
Intravenous
Trodusquemine (MSI-1436) inhibits protein-tyrosine phosphatase 1B (PTB1B) with an IC50 of appr 1 uM, 200-fold preference over TCPTP (IC50, 224 uM). MSI-1436 (10 uM) restores ERK phosphorylation in response to mGluR1/5 agonist DHPG in F11 neuronal cells. MSI-1436 (10 uM) rescues DHPG-induced holding currents and restores DSI in LMO4KO BLA neurons.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:50:16 GMT 2025
by
admin
on
Mon Mar 31 22:50:16 GMT 2025
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| Record UNII |
7VON0S1S42
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| Record Status |
Validated (UNII)
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| Record Version |
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Common Name | English | ||
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Preferred Name | English |
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FDA ORPHAN DRUG |
800120
Created by
admin on Mon Mar 31 22:50:16 GMT 2025 , Edited by admin on Mon Mar 31 22:50:16 GMT 2025
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DBSALT002006
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7VON0S1S42
Created by
admin on Mon Mar 31 22:50:16 GMT 2025 , Edited by admin on Mon Mar 31 22:50:16 GMT 2025
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76957349
Created by
admin on Mon Mar 31 22:50:16 GMT 2025 , Edited by admin on Mon Mar 31 22:50:16 GMT 2025
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PRIMARY |
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |