Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C38H20B20N6O6.Cu |
| Molecular Weight | 936.368 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Cu++].[O-][N+](=O)C1=C2[N-]C(C=C2)=C(C3=NC(C=C3)=C(C4=CC=C([N-]4)C(=C5C=CC1=N5)C6=CC(OC[C]789%10[B]%11%12%13[B]%14%15%16[B]%17%18%19[B]%11%14%20[B]%17%21%22[B]%18%23%24[B]%15%19%25[B]7%12%16[B]8%23%25[C]9%21%24[B]%10%13%20%22)=CC=C6)[N+]([O-])=O)C%26=CC=CC(OC[C]%27%28%29%30[B]%31%32%33[B]%34%35%36[B]%37%38%39[B]%31%34%40[B]%37%41%42[B]%38%43%44[B]%35%39%45[B]%27%32%36[B]%28%43%45[C]%29%41%44[B]%30%33%40%42)=C%26
InChI
InChIKey=GJNAQHWCHVFMKD-XSUIMNIJSA-N
InChI=1S/C38H20B20N6O6.Cu/c65-63(66)33-27-11-7-23(59-27)31(19-3-1-5-21(15-19)69-17-37-35-39(37)43(35)44(35)40(35,37)48(37)47(37,39)51(39,43)55(43,44)52(40,44,48)57(47,48,51)55)24-8-12-28(60-24)34(64(67)68)30-14-10-26(62-30)32(25-9-13-29(33)61-25)20-4-2-6-22(16-20)70-18-38-36-41(38)45(36)46(36)42(36,38)50(38)49(38,41)53(41,45)56(45,46)54(42,46,50)58(49,50,53)56;/h1-16H,17-18H2;/q-2;+2/b31-23-,31-24-,32-25-,32-26-,33-27+,33-29+,34-28+,34-30+;
| Molecular Formula | C38H20B20N6O6 |
| Molecular Weight | 872.822 |
| Charge | -2 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | Cu |
| Molecular Weight | 63.546 |
| Charge | 2 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 10:43:06 GMT 2025
by
admin
on
Wed Apr 02 10:43:06 GMT 2025
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| Record UNII |
6LEC6S4MTY
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| Record Status |
Validated (UNII)
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| Record Version |
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6LEC6S4MTY
Created by
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1030303-53-7
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100000183875
Created by
admin on Wed Apr 02 10:43:06 GMT 2025 , Edited by admin on Wed Apr 02 10:43:06 GMT 2025
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
Drugs: MTL 005(Primary), Cisplatin; Indication: For Head and neck cancer; Focus: Adverse reactions, First in man; Sponsor: MorEx Development Partners; Most Recent Events: 27 Mar 2015 New trial record, 11 Mar 2015 Part 1 of this trial has been completed and preliminary data have been reported at the 30th Conference on Clinical and Experimental Research in Radiation Oncology (CERRO), according to a MorEx media release.
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ACTIVE MOIETY |
Originator: Morvus Technology; Developer: MorEx Development Partners; Class: Metalloporphyrin, Radiation-sensitising agent, Radiosensitiser; Mechanism of Action: Reactive oxygen species stimulant; Orphan Drug Status: Yes for Head and neck cancer; On Fast track: No; New Molecular Entity: Yes; Available For Licensing: Yes; Highest Development Phases: Phase I for Head and neck cancer, Preclinical for Breast cancer; Most Recent Events: 26 Mar 2015 MTL 005 is available for licensing as of 26 Mar 2015. http://www.morexdevelopments.com/partnering.html
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ACTIVE MOIETY |
MTL-005 is a boronated metalloporphyrin in development as a radio-enhancer: a drug given to patients prior to conventional radiotherapy and designed to amplify the effect of radiotherapy within the tumour, without affecting surrounding cells. It does not appear to be pharmacologically active and, as such, it is expected to have a good safety profile.
Structure of MTL-005: (copper meso-5, 15-Bis(3-(( 1,2-Dicarba-closododecaboranyl)methoxy)phenyl)-meso-10,20-dinitroporphyrin)
MTL-005 preferentially accumulates in tumour cells and interacts with the X-rays to generate reactive oxygen species that selectively kill the tumour cells. Evidence suggests that MTL-005 can enhance the effects of radiation regardless of the oxygen status of the target tumour.
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