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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H22ClF3N6O3
Molecular Weight 546.929
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TELOTRISTAT

SMILES

CC1=NN(C=C1)C2=C(C=CC(Cl)=C2)[C@@H](OC3=NC(N)=NC(=C3)C4=CC=C(C[C@H](N)C(O)=O)C=C4)C(F)(F)F

InChI

InChIKey=NCLGDOBQAWBXRA-PGRDOPGGSA-N
InChI=1S/C25H22ClF3N6O3/c1-13-8-9-35(34-13)20-11-16(26)6-7-17(20)22(25(27,28)29)38-21-12-19(32-24(31)33-21)15-4-2-14(3-5-15)10-18(30)23(36)37/h2-9,11-12,18,22H,10,30H2,1H3,(H,36,37)(H2,31,32,33)/t18-,22+/m0/s1

HIDE SMILES / InChI

Molecular Formula C25H22ClF3N6O3
Molecular Weight 546.929
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

Telotristat (telotristat etiprate) is an ethyl ester prodrug which is hydrolyzed to its active moiety LP-778902 both in vivo and in vitro. Telotristat etiprate is an orally bioavailable, small-molecule, tryptophan hydroxylase (TPH) inhibitor. It is the first investigational drug in clinical studies to target TPH, an enzyme that triggers the excess serotonin production within metastatic neuroendocrine tumor (mNET) cells leading to carcinoid syndrome. Unlike existing treatments of carcinoid syndrome which reduce the release of serotonin outside tumor cells, telotristat etiprate reduces serotonin production within the tumor cells. By specifically inhibiting serotonin production telotristat may provide patients with more control over their disease. Telotristat etiprate has received Fast Track and Orphan Drug designation from the U.S. Food and Drug Administration and has been granted priority review by the FDA with a Prescription Drug User Fee Act (PDUFA) target action date of February 28, 2017.

CNS Activity

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
1210.0 nM [IC50]
800.0 nM [IC50]
32.0 nM [IC50]
28.0 nM [IC50]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
XERMELO

Cmax

ValueDoseCo-administeredAnalytePopulation
610 ng/mL
500 mg single, oral
TELOTRISTAT plasma
Homo sapiens

AUC

ValueDoseCo-administeredAnalytePopulation
2320 ng × h/mL
500 mg single, oral
TELOTRISTAT plasma
Homo sapiens

T1/2

ValueDoseCo-administeredAnalytePopulation
5 h
500 mg single, oral
TELOTRISTAT plasma
Homo sapiens

Funbound

ValueDoseCo-administeredAnalytePopulation
1%
500 mg single, oral
TELOTRISTAT plasma
Homo sapiens

Doses

AEs

Drug as perpetrator​

Drug as victim

Tox targets

PubMed

Sample Use Guides

In Vivo Use Guide
Two 250 mg telotristat etiprate tablets three times daily over 12 weeks
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Record UNII
381V4FCV2Z
Record Status Validated (UNII)
Record Version