SCHEMBL164409

SCHEMBL164409

O=S(=O)(c1cc[c]cc1)c1ccccc1

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR6 P50406 7/20 0.70
ALDH1A1 P00352 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
TSHR P16473 2/20 0.44
CA12 O43570 2/20 0.44
CA1 P00915 2/20 0.44
CA2 P00918 2/20 0.44
CA7 P43166 2/20 0.44
CA13 Q8N1Q1 2/20 0.44
HSD17B10 Q99714 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
CA3 P07451 1/20 0.44
CA4 P22748 1/20 0.44
CA6 P23280 1/20 0.44
CA5A P35218 1/20 0.44
PLA2G7 Q13093 1/20 0.44
CA9 Q16790 1/20 0.44
CA14 Q9ULX7 1/20 0.44
CA5B Q9Y2D0 1/20 0.44
KMT2A Q03164 1/20 0.44

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
SCHEMBL818508 0.89 HTR6 (0.50) HTR6ALDH1A1TSHRHSD17B10KMT2A
SCHEMBL27404576 0.87 HTR6 (0.58) HTR6ALDH1A1SMN1; SMN2TSHRCA12
SCHEMBL28198594 0.87 HTR6 (0.52) HTR6ALDH1A1CA12CA1CA2
(Phenylsulfonyl)Benzene SCHEMBL5537560 0.87 HTR6 (0.93) HTR6ALDH1A1SMN1; SMN2TSHRCA12
(Phenylsulfonyl)Benzene SCHEMBL1549229 0.87 HTR6 (0.93) HTR6ALDH1A1SMN1; SMN2TSHRCA12
(Phenylsulfonyl)Benzene SCHEMBL29775288 0.84 HTR6 (1.00) HTR6ALDH1A1SMN1; SMN2TSHRCA12
(Phenylsulfonyl)Benzene SCHEMBL13735236 0.84 HTR6 (1.00) HTR6ALDH1A1SMN1; SMN2TSHRCA12
(Phenylsulfonyl)Benzene SCHEMBL30255 0.84 HTR6 (1.00) HTR6ALDH1A1SMN1; SMN2TSHRCA12
(Phenylsulfonyl)Benzene SCHEMBL29473549 0.84 HTR6 (1.00) HTR6ALDH1A1SMN1; SMN2TSHRCA12
(Phenylsulfonyl)Benzene SCHEMBL29450723 0.84 HTR6 (1.00) HTR6ALDH1A1SMN1; SMN2TSHRCA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3189049-B1 PHTHALAZINE DERIVATIVES OF FORMULA (I) AS PCAF AND GCN5 INHIBITORS FOR USE IN THE TREATMENT OF CANCER GENENTECH INC (US) 2024-03-20 EP claimed
CN-113831340-B Can [ n ] dihydroacridine macrocycle and preparation method thereof 中国科学院化学研究所 2023-04-18 CN claimed
CN-108117548-B Spirofluorene compound, application thereof, thermal activation delayed fluorescence material and organic electroluminescent device using spirofluorene compound 北京鼎材科技有限公司 2022-01-28 CN claimed
CN-113831340-A Calix [ n ] dihydroacridine macrocycle and preparation method thereof 中国科学院化学研究所 2021-12-24 CN claimed
CN-108117495-B Spirofluorene ring compound, use thereof, and organic electroluminescent device using the same 北京鼎材科技有限公司 2021-11-19 CN claimed
CN-107074824-B Phthalazine derivatives of formula (I) as PCAF and GCN5 inhibitors for the treatment of cancer 基因泰克公司 2021-01-08 CN claimed
US-10155764-B2 Therapeutic compounds and uses thereof GENENTECH, INC (US) 2018-12-18 US claimed
CN-108117495-A Spiro fluorene cycle compound, its purposes and use its organic electroluminescence device 北京鼎材科技有限公司 2018-06-05 CN claimed
CN-108117511-A Spiro fluorene cycle compound, its purposes and use its organic electroluminescence device 北京鼎材科技有限公司 2018-06-05 CN claimed
CN-108117548-A Spiro fluorene cycle compound, its application and use its hot activation delayed fluorescence material and organic electroluminescence device 北京鼎材科技有限公司 2018-06-05 CN claimed
EP-0237917-A2 1,1-Disubstituted cyclopropane derivatives, processes for their preparation and their use HOECHST AKTIENGESELLSCHAFT (DE) 1987-09-23 EP claimed
EP-0236700-A1 Alpha,beta-substituted acroleins, process for their production and their use BASF Aktiengesellschaft (DE) 1987-09-16 EP claimed
EP-0236913-A2 Aryl-azolylmethyl-benzocyclo-alkene derivatives, process for their preparation and their use HOECHST AKTIENGESELLSCHAFT (DE) 1987-09-16 EP claimed
CN-85109721-A Preparation has the ectoparasite of the no disease homoiothermic animal of control and the method for endoparasite compositions 1987-07-15 CN claimed
EP-0211004-A1 USE OF ACYL UREA COMPOUNDS FOR CONTROLLING ENDOPARASITES AND ECTOPARASITES OF WARM-BLOODED ANIMALS RHONE-POULENC NEDERLAND B.V. (NL) 1987-02-25 EP claimed
EP-0094038-B1 3-AMINO-6-ARYL-1,2,4-TRIAZOLO(4,3-B)PYRIDAZINES, THEIR PREPARATION AND USE HOECHST AKTIENGESELLSCHAFT (DE) 1987-01-07 EP claimed
WO-1986003941-A1 USE OF ACYL UREA COMPOUNDS FOR CONTROLLING ENDOPARASITES AND ECTOPARASITES OF WARM-BLOODED ANIMALS UNION CARBIDE CORPORATION (US) 1986-07-17 WO claimed
EP-0121490-A1 Substituted 6-aryl-1,2,4-triazolo[4,3-b]pyridazines, their preparation and use HOECHST AKTIENGESELLSCHAFT (DE) 1984-10-10 EP claimed
EP-0094038-A1 3-Amino-6-aryl-1,2,4-triazolo(4,3-b)pyridazines, their preparation and use HOECHST AKTIENGESELLSCHAFT (DE) 1983-11-16 EP claimed
US-4048153-A Azo dyes having an optionally substituted 1-azo-3-nitro-4-arylaminophenyl nucleus SANDOZ LTD. (CH) 1977-09-13 US claimed

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-10155764-B2 Therapeutic compounds and uses thereof HDAC10, HDAC6, HDAC1 HTR6 3724/4885ALDH1A1 2604/4885SMN1; SMN2 520/4885

“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.