Fabesetron

Fabesetron

SCHEMBL1021975

Cc1[nH]cnc1CC1CCc2c(C)c3ccccc3n2C1=O

nearest known ligand 0.47

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR3A P46098 3/20 0.47
CYP3A4 P08684 3/20 0.47
KCNH2 Q12809 3/20 0.47
CYP1A2 P05177 2/20 0.47
HTR2B P41595 2/20 0.47
HTR2A P28223 2/20 0.47
HTR2C P28335 2/20 0.47
ADRA2C P18825 1/20 0.47
ADRA1A P35348 1/20 0.47
CASP6 P55212 1/20 0.46
HTR3E A5X5Y0 2/20 0.39
HTR3B O95264 2/20 0.39
HTR3D Q70Z44 2/20 0.39
HTR3C Q8WXA8 2/20 0.39
CYP2D6 P10635 1/20 0.38
SLC22A2 O15244 1/20 0.38
SLC22A1 O15245 1/20 0.38
SLC22A3 O75751 1/20 0.38
CHRNB2 P17787 1/20 0.38
CHRNB4 P30926 1/20 0.38

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Fabesetron SCHEMBL1350066 1.00 HTR3A (0.47) HTR3ACYP3A4KCNH2CYP1A2HTR2B
Fabesetron SCHEMBL30949355 1.00 HTR3A (0.47) HTR3ACYP3A4KCNH2CYP1A2HTR2B
Fabesetron SCHEMBL2232218 0.99 CASP6 (0.48) HTR3ACYP3A4KCNH2CYP1A2HTR2B
Fabesetron SCHEMBL1026223 0.99 CASP6 (0.48) HTR3ACYP3A4KCNH2CYP1A2HTR2B
Fabesetron SCHEMBL8038329 0.98 HTR3A (0.46) HTR3ACYP3A4KCNH2CYP1A2HTR2B
Fabesetron SCHEMBL9292924 0.92 HTR3A (0.42) HTR3ACYP3A4KCNH2CYP1A2HTR2B
Fabesetron SCHEMBL9292920 0.92 HTR3A (0.42) HTR3ACYP3A4KCNH2CYP1A2HTR2B
SCHEMBL7276284 0.89 HTR3A (0.45) HTR3ACYP3A4KCNH2CYP1A2HTR2B
Hydrochloric Acid SCHEMBL7337938 0.88 CASP6 (0.46) HTR3ACYP3A4KCNH2CYP1A2HTR2B
SCHEMBL7267456 0.88 HTR3A (0.37) HTR3ACYP3A4KCNH2CYP1A2HTR2B

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 67 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0993829-B1 TRANSDERMAL PREPARATION CONTAINING SEROTONIN RECEPTOR ANTAGONIST HISAMITSU PHARMACEUTICAL CO (JP) 2011-01-12 EP claimed
EP-1503764-B1 5-HT4 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF HEART FAILURE SERODUS AS (NO) 2010-01-06 EP claimed
EP-1503764-A1 5-HT4 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF HEART FAILURE MEDINNOVA AS (NO) 2005-02-09 EP claimed
WO-2003097065-A1 5-HT4 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF HEART FAILURE MEDINNOVA AS (NO) 2003-11-27 WO claimed
EP-0451538-B1 Use of pyridoindole derivatives in the treatment of ischemic disorders FUJISAWA PHARMACEUTICAL CO (JP) 1996-05-22 EP claimed
EP-0361317-B1 Pyridoindole derivatives and processes for preparation thereof FUJISAWA PHARMACEUTICAL CO (JP) 1995-04-05 EP claimed
US-5290785-A Therapeutic agent for ischemic diseases FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1994-03-01 US claimed
US-5173493-A For treatment or prevention of nausea or vomiting FUJISAWA PHARMACEUTICAL COMPANY, LTD. (JP) 1992-12-22 US claimed
US-5141945-A 5-Hydroxytryptamine antagonists, treatment or prevention of nausea and vomiting FUJISAWA PHARMACEUTICAL COMPANY, LTD. (JP) 1992-08-25 US claimed
EP-0451538-A2 Use of pyridoindole derivatives in the treatment of ischemic disorders FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1991-10-16 EP claimed
EP-0361317-A2 Pyridoindole derivatives and processes for preparation thereof FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1990-04-04 EP claimed
JP-2117675-A None JP disclosed
JP-4270280-A None JP disclosed
US-20090203792-A1 METHODS OF TREATING NON-PAINFUL BLADDER DISORDERS USING ALPHA2DELTA SUBUNIT CALCIUM CHANNEL MODULATORS DYNOGEN PHARMACEUTICALS, INC. (US) 2009-08-13 US disclosed
EP-1152761-B1 USE OF 5-HT3 RECEPTOR ANTAGONISTS FOR TREATING MUSCULOESKELETAL DISEASES NOVASEARCH AG (CH) 2009-06-24 EP disclosed
JP-H04270280-A THERAPEUTIC AGENT FOR ISCHEMIC DISEASE FUJISAWA PHARMACEUT CO LTD 1992-09-25 JP disclosed
US-5141945-A 5-Hydroxytryptamine antagonists, treatment or prevention of nausea and vomiting FUJISAWA PHARMACEUTICAL COMPANY, LTD. (JP) 1992-08-25 US disclosed
EP-0451538-A2 Use of pyridoindole derivatives in the treatment of ischemic disorders FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1991-10-16 EP disclosed
JP-H02117675-A PYRIDOINDOL DERIVATIVE AND PRODUCTION THEREOF FUJISAWA PHARMACEUT CO LTD 1990-05-02 JP disclosed
EP-0361317-A2 Pyridoindole derivatives and processes for preparation thereof FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1990-04-04 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20090203792-A1 METHODS OF TREATING NON-PAINFUL BLADDER DISORDERS USING ALPHA2DELTA SUBUNIT CALCIUM CHANNEL MODULATORS GABRB2, CACNA1D, CACNA1B HTR3A 468/4885CYP3A4 1997/4885KCNH2 333/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.