Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C47H64N4O12 |
Molecular Weight | 877.0307 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 9 / 9 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CO[C@H]1\C=C\O[C@@]2(C)OC3=C(C2=O)C4=C(O)C(\C=N\N5CCN(CC5)C6CCCC6)=C(NC(=O)C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)C(O)=C4C(O)=C3C
InChI
InChIKey=WDZCUPBHRAEYDL-GZAUEHORSA-N
InChI=1S/C47H64N4O12/c1-24-13-12-14-25(2)46(59)49-37-32(23-48-51-20-18-50(19-21-51)31-15-10-11-16-31)41(56)34-35(42(37)57)40(55)29(6)44-36(34)45(58)47(8,63-44)61-22-17-33(60-9)26(3)43(62-30(7)52)28(5)39(54)27(4)38(24)53/h12-14,17,22-24,26-28,31,33,38-39,43,53-57H,10-11,15-16,18-21H2,1-9H3,(H,49,59)/b13-12+,22-17+,25-14-,48-23+/t24-,26+,27+,28+,33-,38-,39+,43+,47-/m0/s1
Molecular Formula | C47H64N4O12 |
Molecular Weight | 877.0307 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 9 / 9 |
E/Z Centers | 1 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:32:18 UTC 2023
by
admin
on
Sat Dec 16 17:32:18 UTC 2023
|
Record UNII |
XJM390A33U
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Brand Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C280
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
NDF-RT |
N0000007911
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
FDA ORPHAN DRUG |
89495
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
NDF-RT |
N0000007911
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
NDF-RT |
N0000007911
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
WHO-VATC |
QJ04AB05
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
NDF-RT |
N0000175501
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
FDA ORPHAN DRUG |
89695
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
LIVERTOX |
NBK548547
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
EU-Orphan Drug |
EU/3/10/750
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
FDA ORPHAN DRUG |
89595
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
WHO-ATC |
J04AB05
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
||
|
NDF-RT |
N0000007911
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
SUB10311MIG
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
100000080562
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
m9614
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | Merck Index | ||
|
C66516
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
Rifapentine
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
XJM390A33U
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
DB01201
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
XJM390A33U
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
4765
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
Rifapentine
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
45304
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
DTXSID8041115
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
35617
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | RxNorm | ||
|
X-15
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
61379-65-5
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
262-743-9
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
2378
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
135403821
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY | |||
|
CHEMBL1660
Created by
admin on Sat Dec 16 17:32:19 UTC 2023 , Edited by admin on Sat Dec 16 17:32:19 UTC 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
BINDER->LIGAND |
The bound concentration increased slightly (,2%) as the concentration of 14C-rifapentine increased from 0.5 to 10 mg/ml. At concentrations above 10 mg/ml, protein binding did not appear to vary with increasing concentration.
BINDING
|
||
|
METABOLIC ENZYME -> INDUCER | |||
|
EXCRETED UNCHANGED |
FECAL
|
||
|
SALT/SOLVATE -> PARENT | |||
|
METABOLIC ENZYME -> INDUCER | |||
|
EXCRETED UNCHANGED |
URINE
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
METABOLITE -> PARENT |
URINE
|
||
|
METABOLITE -> PARENT |
FECAL
|
||
|
METABOLITE -> PARENT |
FECAL
|
||
|
METABOLITE -> PARENT |
FECAL
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |
Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
---|---|---|---|---|---|---|
Biological Half-life | PHARMACOKINETIC |
|
ORAL ADMINISTRATION |
|
||
Tmax | PHARMACOKINETIC |
|
ORAL ADMINISTRATION |
|
||