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Details

Stereochemistry ACHIRAL
Molecular Formula C18H12F6N6O.ClH
Molecular Weight 478.779
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of VERDINEXOR HYDROCHLORIDE

SMILES

Cl.FC(F)(F)C1=CC(=CC(=C1)C2=NN(C=N2)\C=C/C(=O)NNC3=NC=CC=C3)C(F)(F)F

InChI

InChIKey=NPOWEDMICNPYHB-YHSAGPEESA-N
InChI=1S/C18H12F6N6O.ClH/c19-17(20,21)12-7-11(8-13(9-12)18(22,23)24)16-26-10-30(29-16)6-4-15(31)28-27-14-3-1-2-5-25-14;/h1-10H,(H,25,27)(H,28,31);1H/b6-4-;

HIDE SMILES / InChI

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

Molecular Formula C18H12F6N6O
Molecular Weight 442.3179
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Verdinexor (KPT-335) is a small-molecule selective inhibitor of nuclear export (SINE). Karyopharm Therapeutics has recently developed first-in-class, novel SINE compounds using molecular modeling to screen a small virtual library of compounds against the NES groove of human exportin-1 (XPO1). These compounds inhibit nuclear-cytoplasmic export by reversibly binding to the cargo recognition site of XPO1 and are orally bioavailable. Verdinexor was shown to potently and selectively inhibit vRNP export and effectively inhibited the replication of various influenza virus A and B strains in vitro, including pandemic H1N1 virus, highly pathogenic H5N1 avian influenza virus, and the recently emerged H7N9 strain. Verdinexor is in development for the treatment of viral indications. Verdinexor is being evaluated for the treatment of lymphomas in pet dogs with newly-diagnosed or first relapse after chemotherapy lymphomas.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

Sample Use Guides

A Phase 1, randomized, double-blind, placebo-controlled, sequential, dose-escalating (5-100 mg) trial was conducted to evaluate the safety and tolerability of oral Verdinexor (KPT-335) in healthy adult subjects
Route of Administration: Oral
Verdinexor was found to have good efficacy against the influenza A and B virus strains tested in the nanomolar range (SI of 99), except against the emerging A/Anhui/1/2013 (H7N9) strain, against which it showed some but limited efficacy (SI of 64).
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:08:19 UTC 2023
Edited
by admin
on Sat Dec 16 10:08:19 UTC 2023
Record UNII
3R2O141875
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VERDINEXOR HYDROCHLORIDE
Common Name English
2-PROPENOIC ACID, 3-(3-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)-1H-1,2,4-TRIAZOL-1-YL)-, 2-(2-PYRIDINYL)HYDRAZIDE, HYDROCHLORIDE (1:1), (2Z)-
Systematic Name English
Code System Code Type Description
SMS_ID
300000017202
Created by admin on Sat Dec 16 10:08:19 UTC 2023 , Edited by admin on Sat Dec 16 10:08:19 UTC 2023
PRIMARY
FDA UNII
3R2O141875
Created by admin on Sat Dec 16 10:08:19 UTC 2023 , Edited by admin on Sat Dec 16 10:08:19 UTC 2023
PRIMARY
CAS
1421923-73-0
Created by admin on Sat Dec 16 10:08:19 UTC 2023 , Edited by admin on Sat Dec 16 10:08:19 UTC 2023
PRIMARY
DRUG BANK
DBSALT002155
Created by admin on Sat Dec 16 10:08:19 UTC 2023 , Edited by admin on Sat Dec 16 10:08:19 UTC 2023
PRIMARY
PUBCHEM
73425535
Created by admin on Sat Dec 16 10:08:19 UTC 2023 , Edited by admin on Sat Dec 16 10:08:19 UTC 2023
PRIMARY
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