Alosetron

Alosetron

SCHEMBL13345838

[2H]C([2H])([2H])n1c2c(c3ccccc31)C(=O)N(Cc1nc[nH]c1C)CC2

nearest known ligand 0.86

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HTR3A

The experimentally established mechanism targets of Alosetron. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
HTR3A known ✓ P46098 2/20 0.86
KCNH2 Q12809 2/20 0.86
CYP1A2 P05177 1/20 0.86
CYP3A4 P08684 1/20 0.86
ADRA2C P18825 1/20 0.86
HTR2A P28223 1/20 0.86
HTR2C P28335 1/20 0.86
ADRA1A P35348 1/20 0.86
HTR2B P41595 1/20 0.86
CASP6 P55212 1/20 0.85
CD44 P16070 1/20 0.41
WDR5 P61964 1/20 0.38
KMT2A Q03164 1/20 0.38
HTR3E A5X5Y0 1/20 0.37
HTR3B O95264 1/20 0.37
HTR3D Q70Z44 1/20 0.37
HTR3C Q8WXA8 1/20 0.37

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
Alosetron SCHEMBL631 0.93 KCNH2 (1.00) KCNH2HTR3ACYP1A2CYP3A4ADRA2C
Alosetron SCHEMBL29377019 0.93 KCNH2 (1.00) KCNH2HTR3ACYP1A2CYP3A4ADRA2C
Alosetron SCHEMBL806 0.92 CASP6 (1.00) KCNH2HTR3ACYP1A2CYP3A4ADRA2C
Alosetron SCHEMBL29387635 0.92 CASP6 (1.00) KCNH2HTR3ACYP1A2CYP3A4ADRA2C
Alosetron SCHEMBL13345850 0.91 KCNH2 (0.72) KCNH2HTR3ACYP1A2CYP3A4ADRA2C
Alosetron SCHEMBL635233 0.91 KCNH2 (0.96) KCNH2HTR3ACYP1A2CYP3A4ADRA2C
Alosetron SCHEMBL850 0.88 KCNH2 (0.90) KCNH2HTR3ACYP1A2CYP3A4ADRA2C
Alosetron SCHEMBL13345849 0.88 HTR3A (0.67) KCNH2HTR3ACYP1A2CYP3A4ADRA2C
SCHEMBL837 0.87 KCNH2 (0.88) KCNH2HTR3ACYP1A2CYP3A4ADRA2C
Alosetron SCHEMBL13345832 0.86 KCNH2 (0.65) KCNH2HTR3ACYP1A2CYP3A4ADRA2C

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 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100113478-A1 INDOLONE MODULATORS OF 5-HT3 RECEPTOR AUSPEX PHARMACEUTICALS, INC. (US) 2010-05-06 US 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-20100113478-A1 INDOLONE MODULATORS OF 5-HT3 RECEPTOR HTR3A, HTR3B, HTR3E HTR3A 1/4885KCNH2 1673/4885CYP1A2 1126/4885

“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.