U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C61H88N18O21S2
Molecular Weight 1473.589
Optical Activity UNSPECIFIED
Defined Stereocenters 20 / 20
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PEPLOMYCIN

SMILES

[H][C@]7(O[C@@H]1[C@H](O[C@H]([C@H](NC(=O)C2=NC(=NC(N)=C2C)[C@H](CC(N)=O)NC[C@H](N)C(N)=O)C(=O)N[C@H](C)[C@@H](O)[C@H](C)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCCC3=NC(=CS3)C4=NC(=CS4)C(=O)NCCCN[C@@H](C)C5=CC=CC=C5)C6=CN=CN6)O[C@@H](CO)[C@@H](O)[C@@H]1O)O[C@H](CO)[C@@H](O)[C@H](OC(N)=O)[C@@H]7O

InChI

InChIKey=QIMGFXOHTOXMQP-GFAGFCTOSA-N
InChI=1S/C61H88N18O21S2/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/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)/t25-,26-,27+,28+,30-,31-,35-,36+,40-,41-,42-,43+,44+,45-,46-,47-,48-,49-,59+,60-/m0/s1

HIDE SMILES / InChI

Description
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

Curator's Comment: https://www.google.ch/patents/US4238391

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Pepleo

Approved Use

It is used for the treatment of skin cancer, head and neck malignancy, lung cancer, prostate cancer, malignant lymphoma
Primary
Pepleo

Approved Use

It is used for the treatment of skin cancer, head and neck malignancy, lung cancer, prostate cancer, malignant lymphoma
Primary
Pepleo

Approved Use

It is used for the treatment of skin cancer, head and neck malignancy, lung cancer, prostate cancer, malignant lymphoma
Primary
Pepleo

Approved Use

It is used for the treatment of skin cancer, head and neck malignancy, lung cancer, prostate cancer, malignant lymphoma
Primary
Pepleo

Approved Use

It is used for the treatment of skin cancer, head and neck malignancy, lung cancer, prostate cancer, malignant lymphoma
PubMed

PubMed

TitleDatePubMed
Effect of pepleomycin in prostatic cancer. A preliminary report.
1980
Patents

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
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.
Name Type Language
PEPLOMYCIN
INN   JAN   MI   WHO-DD  
INN  
Official Name English
N(SUP 1)-(3-(((1S)-1-PHENYLETHYL)AMINO)PROPYL)BLEOMYCINAMIDE
Common Name English
N(SUP 1)-(3-(((S)-.ALPHA.-METHYLBENZYL)AMINO)PROPYL)BLEOMYCINAMIDE
Common Name English
PEPLEOMYCIN
Common Name English
Peplomycin [WHO-DD]
Common Name English
peplomycin [INN]
Common Name English
PEPLOMYCIN [MI]
Common Name English
PEPLOMYCIN [JAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C2311
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2111003
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
PUBCHEM
6852373
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
DRUG CENTRAL
2965
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
CAS
68247-85-8
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
MESH
D017663
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
EVMPD
SUB09708MIG
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
FDA UNII
56H9L80NIZ
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
NCI_THESAURUS
C1399
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
ECHA (EC/EINECS)
269-484-0
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
INN
4833
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
EPA CompTox
DTXSID701024414
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY
MERCK INDEX
m8527
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY Merck Index
SMS_ID
100000082539
Created by admin on Fri Dec 15 18:38:51 GMT 2023 , Edited by admin on Fri Dec 15 18:38:51 GMT 2023
PRIMARY