Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C61H88N18O21S2.H2O4S |
| Molecular Weight | 1571.668 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 20 / 20 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OS(O)(=O)=O.C[C@@H](O)[C@H](NC(=O)[C@@H](C)[C@H](O)[C@@H](C)NC(=O)[C@@H](NC(=O)C1=NC(=NC(N)=C1C)[C@H](CC(N)=O)NC[C@H](N)C(N)=O)[C@@H](O[C@@H]2O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]2O[C@H]3O[C@H](CO)[C@@H](O)[C@H](OC(N)=O)[C@@H]3O)C4=CN=CN4)C(=O)NCCC5=NC(=CS5)C6=NC(=CS6)C(=O)NCCCN[C@@H](C)C7=CC=CC=C7
InChI
InChIKey=ZHHIHQFAUZZMTG-BSVJBJGJSA-N
InChI=1S/C61H88N18O21S2.H2O4S/c1-24-39(76-52(79-50(24)64)31(16-37(63)83)71-17-30(62)51(65)89)56(93)78-41(47(32-18-67-23-72-32)98-60-49(45(87)43(85)35(19-80)97-60)99-59-46(88)48(100-61(66)95)44(86)36(20-81)96-59)57(94)73-27(4)42(84)25(2)53(90)77-40(28(5)82)55(92)70-15-12-38-74-34(22-101-38)58-75-33(21-102-58)54(91)69-14-9-13-68-26(3)29-10-7-6-8-11-29;1-5(2,3)4/h6-8,10-11,18,21-23,25-28,30-31,35-36,40-49,59-60,68,71,80-82,84-88H,9,12-17,19-20,62H2,1-5H3,(H2,63,83)(H2,65,89)(H2,66,95)(H,67,72)(H,69,91)(H,70,92)(H,73,94)(H,77,90)(H,78,93)(H2,64,76,79);(H2,1,2,3,4)/t25-,26-,27+,28+,30-,31-,35-,36+,40-,41-,42-,43+,44+,45-,46-,47-,48-,49-,59+,60-;/m0./s1
| Molecular Formula | H2O4S |
| Molecular Weight | 98.078 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C61H88N18O21S2 |
| Molecular Weight | 1473.589 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 20 / 20 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionCurator's Comment: description was created based on several sources, including:
https://www.ncbi.nlm.nih.gov/pubmed/83987 | http://www.rad-ar.or.jp/siori/kekka.cgi?n=39236
Curator's Comment: description was created based on several sources, including:
https://www.ncbi.nlm.nih.gov/pubmed/83987 | http://www.rad-ar.or.jp/siori/kekka.cgi?n=39236
Peplomycin has been developed as novel analog of bleomycin, which has less pulmonary toxicity than bleomycin. Peplomycin has been the subject of extensive studies in Japan and Europe. It is indicated for the treatment of malignant lymphoma, head and neck cancer, lung cancer, prostate cancer and skin cancer. General side effects are: digestive symptoms such as stomatitis, anorexia, nausea/vomiting, general malaise, depilation, fever, chills etc.
Originator
Sources: http://iss.ndl.go.jp/books/R000000004-I1917102-00
Curator's Comment: https://www.google.ch/patents/US4238391
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: WP1925 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Pepleo Approved UseIt is used for the treatment of skin cancer, head and neck malignancy, lung cancer, prostate cancer, malignant lymphoma |
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| Primary | Pepleo Approved UseIt is used for the treatment of skin cancer, head and neck malignancy, lung cancer, prostate cancer, malignant lymphoma |
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| Primary | Pepleo Approved UseIt is used for the treatment of skin cancer, head and neck malignancy, lung cancer, prostate cancer, malignant lymphoma |
|||
| Primary | Pepleo Approved UseIt is used for the treatment of skin cancer, head and neck malignancy, lung cancer, prostate cancer, malignant lymphoma |
|||
| Primary | Pepleo Approved UseIt is used for the treatment of skin cancer, head and neck malignancy, lung cancer, prostate cancer, malignant lymphoma |
Sample Use Guides
3.2 mg/m2 once a day, 2-3 times per week (22.4 mg/m2 per week)
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/83987
Peplomycin showed the following antimicrobial potency against Mycobacterium smegmatis ATCC 607 – 873 ug potency/mg and gave the following very correlative result on the growth inhibition of cultured HeLa S3 cells – ID50 = 0.84 ug/ml.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:55:32 GMT 2025
by
admin
on
Mon Mar 31 17:55:32 GMT 2025
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| Record UNII |
6A668951HW
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C2311
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SUB21700
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100000085037
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C1400
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m8527
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274-588-4
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ACTIVE MOIETY |