Details
Stereochemistry | ACHIRAL |
Molecular Formula | C27H36N6O3S |
Molecular Weight | 524.678 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CN=C(NC2=CC=C(OCCN3CCCC3)C=C2)N=C1NC4=CC=CC(=C4)S(=O)(=O)NC(C)(C)C
InChI
InChIKey=JOOXLOJCABQBSG-UHFFFAOYSA-N
InChI=1S/C27H36N6O3S/c1-20-19-28-26(30-21-10-12-23(13-11-21)36-17-16-33-14-5-6-15-33)31-25(20)29-22-8-7-9-24(18-22)37(34,35)32-27(2,3)4/h7-13,18-19,32H,5-6,14-17H2,1-4H3,(H2,28,29,30,31)
Approval Year
Name | Type | Language | ||
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Official Name | English | ||
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Code | English | ||
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Code | English | ||
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Code | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C129825
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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NCI_THESAURUS |
C125450
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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Code System | Code | Type | Description | ||
---|---|---|---|---|---|
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6L1XP550I6
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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TG101348
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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6L1XP550I6
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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m12160
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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AB-104
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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CHEMBL1287853
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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5347
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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DB12500
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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9707
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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DTXSID90239483
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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C88293
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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936091-26-8
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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SUB126288
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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Fedratinib
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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16722836
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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2197490
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY | |||
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100000151872
Created by
admin on Sat Dec 16 01:55:21 UTC 2023 , Edited by admin on Sat Dec 16 01:55:21 UTC 2023
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PRIMARY |
ACTIVE MOIETY
METABOLITE (PARENT)
METABOLITE LESS ACTIVE (PARENT)
SALT/SOLVATE (PARENT)
SALT/SOLVATE (PARENT)