SCHEMBL2182107

SCHEMBL2182107

CN1CCC[C@H]1Cc1c[nH]c2ccc(Br)cc12

nearest known ligand 0.76

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
HTR1B P28222 8/20 0.76
HTR1D P28221 5/20 0.76
HTR1A P08908 3/20 0.71
HTR6 P50406 10/20 0.69
CHRM2 P08172 1/20 0.58
ADRA2A P08913 1/20 0.58
CHRM1 P11229 1/20 0.58
DRD1 P21728 1/20 0.58
SLC6A2 P23975 1/20 0.58
OPRM1 P35372 1/20 0.58
SLC6A3 Q01959 1/20 0.58
HRH3 Q9Y5N1 1/20 0.58

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
SCHEMBL697582 1.00 HTR1B (0.76) HTR1BHTR1DHTR1AHTR6CHRM2
SCHEMBL772429 1.00 HTR1B (0.76) HTR1BHTR1DHTR1AHTR6CHRM2
SCHEMBL29827195 1.00 HTR1B (0.76) HTR1BHTR1DHTR1AHTR6CHRM2
Oxalic Acid SCHEMBL2727283 0.94 HTR1B (0.68) HTR1BHTR1DHTR1AHTR6CHRM2
Oxalic Acid SCHEMBL2725284 0.94 HTR1B (0.68) HTR1BHTR1DHTR1AHTR6CHRM2
Fumaric Acid SCHEMBL2180504 0.90 HTR1B (0.63) HTR1BHTR1DHTR1AHTR6CHRM2
Fumaric Acid SCHEMBL2182475 0.90 HTR1B (0.63) HTR1BHTR1DHTR1AHTR6CHRM2
SCHEMBL8888890 0.87 HTR1B (0.60) HTR1BHTR1DHTR1AHTR6
SCHEMBL8508432 0.86 HTR1B (1.00) HTR1BHTR1DHTR1AHTR6CHRM2
SCHEMBL8208343 0.86 HTR1B (1.00) HTR1BHTR1DHTR1AHTR6CHRM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2421853-B1 SYNTHESIS OF 3-{[(2R)-1-METHYLPYRROLIDIN-2-YL]METHYL}-5-[2-(PHENYLSULFONYL)ETHYL]-1H-INDOLE ITALIANA SINT SPA (IT) 2013-07-24 EP disclosed
US-8426612-B2 Synthesis of 3-{[(2R)-1-methylpyrrolidin-2-yl]methyl}-5[2-(phenylsulfonyl)ethyl]-1H-indole F.I.S. FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2013-04-23 US disclosed
US-20120071669-A1 PROCESS FOR PREPARATION OF ELETRIPTAN AND SALT THEREOF USV Limited B.S.D. Mar (IN) 2012-03-22 US disclosed
US-20110166364-A1 SYNTHESIS OF 3--5-[2-(PHENYLSULFONYL)ETHYL]-1H-INDOLE F.I.S. FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2011-07-07 US disclosed
CN-1289479-C As 5-HT1D5-ring indole compounds of receptor ligands ALLELIX BIOPHARMA (CA) 2006-12-13 CN disclosed
EP-0944595-B1 5-CYCLO INDOLE COMPOUNDS AS 5-HT1D RECEPTOR LIGANDS NPS ALLELIX CORP (CA) 2003-10-01 EP disclosed
EP-1098896-B1 5-BICYCLOINDOLE COMPOUNDS NPS ALLELIX CORP (CA) 2003-06-25 EP disclosed
CN-1245491-A 5-cyclo indole compounds as 5-HT receptor ligands ALLELIX BIOPHARMA (CA) 2000-02-23 CN disclosed
US-5998438-A SEROTONIN RECEPTOR ANTAGONIST; HEADACHE THERAPY ALLELIX BIOPHARMACEUTICALS, INC. (CA) 1999-12-07 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 (2 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-20120071669-A1 PROCESS FOR PREPARATION OF ELETRIPTAN AND SALT THEREOF HTR3C, SLC6A4, HTR3A HTR1B 21/4885HTR1D 26/4885HTR1A 12/4885
US-20110166364-A1 SYNTHESIS OF 3--5-[2-(PHENYLSULFONYL)ETHYL]-1H-INDOLE TMPRSS15, PEPD, DPP9 HTR1B 254/4885HTR1D 137/4885HTR1A 42/4885

“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.