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Details

Stereochemistry ACHIRAL
Molecular Formula C30H34N4O2.ClH
Molecular Weight 519.078
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Alectinib Hydrochloride

SMILES

Cl.CCC1=C(C=C2C(=C1)C(=O)C3=C(NC4=C3C=CC(=C4)C#N)C2(C)C)N5CCC(CC5)N6CCOCC6

InChI

InChIKey=GYABBVHSRIHYJR-UHFFFAOYSA-N
InChI=1S/C30H34N4O2.ClH/c1-4-20-16-23-24(17-26(20)34-9-7-21(8-10-34)33-11-13-36-14-12-33)30(2,3)29-27(28(23)35)22-6-5-19(18-31)15-25(22)32-29;/h5-6,15-17,21,32H,4,7-14H2,1-3H3;1H

HIDE SMILES / InChI

Molecular Formula C30H34N4O2
Molecular Weight 482.6166
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
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 Sat Dec 16 05:32:12 UTC 2023
Edited
by admin
on Sat Dec 16 05:32:12 UTC 2023
Record UNII
P9YY73LO6J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Alectinib Hydrochloride
WHO-DD  
JAN  
Official Name English
Alectinib hydrochloride [WHO-DD]
Common Name English
ALECTINIB HYDROCHLORIDE [ORANGE BOOK]
Common Name English
CH-5424802 HYDROCHLORIDE
Code English
ALECTINIB HYDROCHLORIDE [JAN]
Common Name English
ALECENSA
Brand Name English
5H-BENZO(B)CARBAZOLE-3-CARBONITRILE, 9-ETHYL-6,11-DIHYDRO-6,6-DIMETHYL-8-(4-(4-MORPHOLINYL)-1-PIPERIDINYL)-11-OXO-, HYDROCHLORIDE (1:1)
Systematic Name English
ALECTINIB HYDROCHLORIDE [MI]
Common Name English
AF-802 HYDROCHLORIDE
Code English
Code System Code Type Description
ChEMBL
CHEMBL1738797
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
JAPANESE REVIEW
ALECENSA
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY APPROVE JULY 2014
DAILYMED
P9YY73LO6J
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
CAS
1256589-74-8
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
FDA UNII
P9YY73LO6J
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
EVMPD
SUB177048
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
SMS_ID
100000162855
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
RXCUI
1727454
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY RxNorm
CHEBI
62268
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
EPA CompTox
DTXSID10154841
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
DRUG BANK
DBSALT001607
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
PUBCHEM
53239799
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
CAS
1256590-18-7
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
NON-SPECIFIC STOICHIOMETRY
MERCK INDEX
m11898
Created by admin on Sat Dec 16 05:32:12 UTC 2023 , Edited by admin on Sat Dec 16 05:32:12 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY