SCHEMBL260867

SCHEMBL260867

O=S(=O)(c1ccccc1)n1ccc2c(Br)cccc21

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR6 P50406 17/20 0.68
HTR1A P08908 3/20 0.59
HTR1D P28221 2/20 0.59
HTR1B P28222 2/20 0.59
HTR1F P30939 2/20 0.59
HTR7 P34969 2/20 0.59
DRD3 P35462 2/20 0.59
MEN1 O00255 2/20 0.58
HTT P42858 2/20 0.58
KMT2A Q03164 2/20 0.58
ALDH1A1 P00352 1/20 0.58
LMNA P02545 1/20 0.58
HPGD P15428 1/20 0.58
TSHR P16473 1/20 0.58
DRD2 P14416 3/20 0.56
HTR2A P28223 2/20 0.56
HDAC3 O15379 1/20 0.55
HDAC4 P56524 1/20 0.55
HDAC1 Q13547 1/20 0.55
HDAC7 Q8WUI4 1/20 0.55

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
SCHEMBL30644286 1.00 HTR6 (0.68) HTR6HTR1AHTR1DHTR1BHTR1F
SCHEMBL30096985 0.86 HTR6 (0.56) HTR6HTR1AHTR1DHTR1BHTR1F
SCHEMBL505125 0.86 HTR6 (0.56) HTR6HTR1AHTR1DHTR1BHTR1F
SCHEMBL3610149 0.83 HTR6 (0.51) HTR6HTR1AHTR1DHTR1BHTR1F
SCHEMBL5746143 0.81 HTR6 (0.68) HTR6HTR1AHTR1DHTR1BHTR1F
SCHEMBL4019658 0.81 HTR6 (0.68) HTR6HTR1AHTR1DHTR1BHTR1F
SCHEMBL30229336 0.81 HTR6 (0.68) HTR6HTR1AHTR1DHTR1BHTR1F
SCHEMBL29686864 0.81 HTR6 (0.68) HTR6HTR1AHTR1DHTR1BHTR1F
SCHEMBL20843619 0.81 HTR6 (0.68) HTR6HTR1AHTR1DHTR1BHTR1F
SCHEMBL5758119 0.81 HTR6 (1.00) HTR6HTR1AHTR1DHTR1BHTR1F

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025031471-A1 NOVEL HETEROCYCLIC COMPOUND FOR REGULATING P53 FUNCTION 德睿智药(苏州)新药研发有限公司 2025-02-13 WO disclosed
CN-117003770-A Fused pyrimidine compound or pharmaceutically acceptable salt thereof, and preparation method and application thereof 南京师范大学 2023-11-07 CN disclosed
US-20200207741-A1 INHIBITORS OF BRUTON'S TYROSINE KINASE HOFFMANN-LA ROCHE INC. 2020-07-02 US disclosed
US-10640491-B2 Inhibitors of bruton's tyrosine kinase HOFFMANN-LA ROCHE INC. (US) 2020-05-05 US disclosed
US-20180305340-A1 INHIBITORS OF BRUTON'S TYROSINE KINASE HOFFMANN-LA ROCHE INC. 2018-10-25 US disclosed
US-10093657-B2 Inhibitors of bruton's tyrosine kinase HOFFMANN-LA ROCHE INC. (US) 2018-10-09 US disclosed
US-10010554-B2 Fused pyrimidines as inhibitors of P97 complex CLEAVE BIOSCIENCES, INC. (US) 2018-07-03 US disclosed
US-10010554-B2 Fused pyrimidines as inhibitors of P97 complex CLEAVE BIOSCIENCES, INC. (US) 2018-07-03 US disclosed
EP-3080097-B1 INHIBITORS OF BRUTON'S TYROSINE KINASE HOFFMANN LA ROCHE (CH) 2018-04-18 EP disclosed
EP-3080097-B1 INHIBITORS OF BRUTON'S TYROSINE KINASE HOFFMANN LA ROCHE (CH) 2018-04-18 EP disclosed
WO-2007061694-A2 SPIROHYDANTOIN TRICYCLIC CGRP RECEPTOR ANTAGONISTS MERCK & CO., INC. (US) 2007-05-31 WO disclosed
US-7087750-B2 Compounds, their use and preparation BIOVITRUM AB (SE) 2006-08-08 US disclosed
WO-2006031491-A2 TRICYCLIC ANILIDE SPIROLACTAM CGRP RECEPTOR ANTAGONISTS MERCK & CO., INC. (US) 2006-03-23 WO disclosed
CN-1714077-A 2-, 3-, 4-or 5-substituted N1- (phenylsulfonyl) indoles and their therapeutic use BIOVITRUM AB (SE) 2005-12-28 CN disclosed
US-20050256106-A1 Novel compounds, their use and preparation BIOVITRUM AB, A STOCKHOLM, SWEDEN CORPORATION 2005-11-17 US disclosed
EP-1373240-B1 RETINOID X RECEPTOR MODULATORS LILLY CO ELI (US) 2005-06-15 EP disclosed
US-20040167160-A1 Retinoid x receptor modulators LIGAND PHARMACEUTICALS INCORPORATED 2004-08-26 US disclosed
EP-1326830-A1 2-, 3-, 4-, OR 5-SUBSTITUTED-N1-(BENZENSULFONYL)INDOLES AND THEIR USE IN THERAPY BIOVITRUM AB (SE) 2003-07-16 EP disclosed
US-20020165251-A1 Novel compounds, their use and preparation PROXIMAGEN NEUROSCIENCE PLC (GB) 2002-11-07 US disclosed
WO-2002032863-A1 2-, 3-, 4-, OR 5-SUBSTITUTED-N1-(BENZENSULFONYL)INDOLES AND THEIR USE IN THERAPY BIOVITRUM AB (SE) 2002-04-25 WO 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 (8 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-20040167160-A1 Retinoid x receptor modulators RXRA, RXRG, RXRB HTR6 1111/4885HTR1A 899/4885HTR1D 1095/4885
US-20180305340-A1 INHIBITORS OF BRUTON'S TYROSINE KINASE BTK, SYK, LYN HTR6 4290/4885HTR1A 4341/4885HTR1D 4159/4885
US-10093657-B2 Inhibitors of bruton's tyrosine kinase BTK, SYK, LYN HTR6 4290/4885HTR1A 4341/4885HTR1D 4159/4885
US-20020165251-A1 Novel compounds, their use and preparation HTR6, HTR1A, HTR5A HTR6 1/4885HTR1A 2/4885HTR1D 16/4885
US-20200207741-A1 INHIBITORS OF BRUTON'S TYROSINE KINASE BTK, SYK, LYN HTR6 3902/4885HTR1A 4018/4885HTR1D 3918/4885
US-10640491-B2 Inhibitors of bruton's tyrosine kinase BTK, SYK, LYN HTR6 4290/4885HTR1A 4341/4885HTR1D 4159/4885
US-10010554-B2 Fused pyrimidines as inhibitors of P97 complex PSMG3, PSME1, PSMB1 HTR6 4171/4885HTR1A 4083/4885HTR1D 4338/4885
US-20050256106-A1 Novel compounds, their use and preparation HTR6, HTR3C, HTR1A HTR6 1/4885HTR1A 3/4885HTR1D 19/4885

“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.