SCHEMBL975190

SCHEMBL975190

O=S(=O)(O)c1cccc(-c2cccc(S(=O)(=O)O)c2)c1

nearest known ligand 0.61

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.61
ALDH1A1 P00352 3/20 0.61
HSD17B10 Q99714 2/20 0.61
TDP1 Q9NUW8 1/20 0.61
SMN1; SMN2 Q16637 1/20 0.56
CA2 P00918 3/20 0.45
CA12 O43570 2/20 0.45
CA9 Q16790 2/20 0.45
NAPRT Q6XQN6 1/20 0.45
HSD17B1 P14061 3/20 0.44
HSD17B2 P37059 3/20 0.44
CA1 P00915 2/20 0.42
LMNA P02545 1/20 0.42
HDAC6 Q9UBN7 1/20 0.42
PFKFB3 Q16875 1/20 0.41
SYK P43405 1/20 0.41
NT5E P21589 1/20 0.41
SNCA P37840 1/20 0.40
PTPN1 P18031 1/20 0.40

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
SCHEMBL27903792 0.98 TSHR (0.59) TSHRALDH1A1HSD17B10TDP1SMN1; SMN2
SCHEMBL5081851 0.98 TSHR (0.59) TSHRALDH1A1HSD17B10TDP1SMN1; SMN2
SCHEMBL1416443 0.98 TSHR (0.59) TSHRALDH1A1HSD17B10TDP1SMN1; SMN2
SCHEMBL15509798 0.98 TSHR (0.59) TSHRALDH1A1HSD17B10TDP1SMN1; SMN2
SCHEMBL27834040 0.93 ALDH1A1 (0.55) TSHRALDH1A1HSD17B10TDP1SMN1; SMN2
SCHEMBL307044 0.93 TSHR (0.62) TSHRALDH1A1HSD17B10TDP1SMN1; SMN2
Water SCHEMBL15608810 0.91 TSHR (0.60) TSHRALDH1A1HSD17B10TDP1SMN1; SMN2
SCHEMBL10655412 0.91 TSHR (0.54) TSHRALDH1A1HSD17B10TDP1SMN1; SMN2
Hydrochloric Acid SCHEMBL27905022 0.91 TSHR (0.60) TSHRALDH1A1HSD17B10TDP1SMN1; SMN2
SCHEMBL28143195 0.91 TSHR (0.60) TSHRALDH1A1HSD17B10TDP1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106356561-A Overcharge-preventing electrolyte and lithium ion battery 宁德时代新能源科技股份有限公司 2017-01-25 CN claimed
US-4467123-A Process for the preparation of alkali metal diphenylates and free hydroxydiphenyls BAYER AKTIENGESELLSCHAFT (DE) 1984-08-21 US claimed
WO-2024019064-A1 SILICON-CONTAINING RESIST UNDERLAYER FILM-FORMING COMPOSITION CONTAINING POLYFUNCTIONAL SULFONIC ACID 日産化学株式会社 2024-01-25 WO disclosed
US-10562837-B2 Preparation of phenyl compounds NEDERLANDSE ORGANISATIE VOOR TOEGEPAST-NATUURWETENSCHAPPELIJK ONDERZOEK TNO (NL) 2020-02-18 US disclosed
CN-106356561-B Overcharge-preventing electrolyte and lithium ion battery 宁德时代新能源科技股份有限公司 2019-07-30 CN disclosed
WO-2017111598-A1 PREPARATION OF PHENYL COMPOUNDS NEDERLANDSE ORGANISATIE VOOR TOEGEPAST-NATUURWETENSCHAPPELIJK ONDERZOEK TNO (NL) 2017-06-29 WO disclosed
EP-3184507-A1 PREPARATION OF PHENYL COMPOUNDS Nederlandse Organisatie voor toegepast- natuurwetenschappelijk onderzoek TNO (NL) 2017-06-28 EP disclosed
CN-106356561-A Overcharge-preventing electrolyte and lithium ion battery 宁德时代新能源科技股份有限公司 2017-01-25 CN disclosed
CN-103965082-B Contain the preparation method of the Phenylsulfonic acid sulfonate of amino and phenolic group HARBIN INSTITUTE OF TECHNOLOGY (CN) 2015-08-19 CN disclosed
CN-103965082-A Benzene sulfonates containing amino and phenolic group and preparation method thereof HARBIN INST OF TECHNOLOGY 2014-08-06 CN disclosed
US-8563645-B2 Thermoplastic resin composition and resin molded product MITSUBISHI ENGINEERING-PLASTICS CORPORATION (JP) 2013-10-22 US disclosed
EP-0281898-B1 REACTIVE DYES BAYER AG (DE) 1991-07-10 EP disclosed
US-4808193-A Process for dyeing hydroxy-containing fiber material with water-soluble dis-azo reactive dye compound HOECHST AKTIENGESELLSCHAFT (DE) 1989-02-28 US disclosed
US-4788011-A Process for the preparation of chemical compounds obtained as solids from liquid starting substances BAYER AKTIENGESELLSCHAFT (DE) 1988-11-29 US disclosed
US-4762916-A CELLULOSE FABRICS HOECHST AKTIENGESELLSCHAFT (DE) 1988-08-09 US disclosed
EP-0040806-B1 WATER-SOLUBLE, COLOURED COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THEIR USE AS DYESTUFFS HOECHST AKTIENGESELLSCHAFT (DE) 1984-09-19 EP disclosed
US-4467123-A Process for the preparation of alkali metal diphenylates and free hydroxydiphenyls BAYER AKTIENGESELLSCHAFT (DE) 1984-08-21 US disclosed
US-4115354-A METAL SALTS OF AROMATIC SULFONATES GENERAL ELECTRIC COMPANY (US) 1978-09-19 US disclosed
US-4011160-A OR OXAZINE-MODIFIED POLYMERS THE DOW CHEMICAL COMPANY (US) 1977-03-08 US disclosed
US-4001147-A OR OXAZINE MODIFIED POLYMERSPOLYSTYRENE, REMOVAL OF PHENOLIC COMPOUNDS THE DOW CHEMICAL COMPANY (US) 1977-01-04 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-10562837-B2 Preparation of phenyl compounds FDPS, DHPS, DDT TSHR 4645/4885ALDH1A1 860/4885HSD17B10 3508/4885

“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.