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Details

Stereochemistry ACHIRAL
Molecular Formula C28H30F2N6
Molecular Weight 488.5748
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Crozbaciclib

SMILES

CN1CCC(CC1)C2=CC=C(NC3=NC=C(F)C(=N3)C4=CC5=C(N=C(C)C56CCCC6)C(F)=C4)N=C2

InChI

InChIKey=AEFFENQISAXIKE-UHFFFAOYSA-N
InChI=1S/C28H30F2N6/c1-17-28(9-3-4-10-28)21-13-20(14-22(29)26(21)33-17)25-23(30)16-32-27(35-25)34-24-6-5-19(15-31-24)18-7-11-36(2)12-8-18/h5-6,13-16,18H,3-4,7-12H2,1-2H3,(H,31,32,34,35)

HIDE SMILES / InChI

Molecular Formula C28H30F2N6
Molecular Weight 488.5748
Charge 0
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 Wed Apr 02 05:03:34 GMT 2025
Edited
by admin
on Wed Apr 02 05:03:34 GMT 2025
Record UNII
5Y2Z8AH65E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Crozbaciclib [INN]
Preferred Name English
Crozbaciclib
INN  
Official Name English
2-PYRIMIDINAMINE, 5-FLUORO-4-(7'-FLUORO-2'-METHYLSPIRO(CYCLOPENTANE-1,3'-(3H)INDOL)-5'-YL)-N-(5-(1-METHYL-4-PIPERIDINYL)-2-PYRIDINYL)-
Systematic Name English
5-fluoro-4-(7'-fluoro-2'-methylspiro[cyclopentane-1,3'- indol]-5'-yl)-N-[5-(1-methylpiperidin-4-yl)pyridin-2- yl]pyrimidin-2-amine
Systematic Name English
Code System Code Type Description
SMS_ID
300000027204
Created by admin on Wed Apr 02 05:03:34 GMT 2025 , Edited by admin on Wed Apr 02 05:03:34 GMT 2025
PRIMARY
NCI_THESAURUS
C203108
Created by admin on Wed Apr 02 05:03:34 GMT 2025 , Edited by admin on Wed Apr 02 05:03:34 GMT 2025
PRIMARY
CAS
2099128-41-1
Created by admin on Wed Apr 02 05:03:34 GMT 2025 , Edited by admin on Wed Apr 02 05:03:34 GMT 2025
PRIMARY
FDA UNII
5Y2Z8AH65E
Created by admin on Wed Apr 02 05:03:34 GMT 2025 , Edited by admin on Wed Apr 02 05:03:34 GMT 2025
PRIMARY
INN
12293
Created by admin on Wed Apr 02 05:03:34 GMT 2025 , Edited by admin on Wed Apr 02 05:03:34 GMT 2025
PRIMARY
PUBCHEM
129202507
Created by admin on Wed Apr 02 05:03:34 GMT 2025 , Edited by admin on Wed Apr 02 05:03:34 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY