SCHEMBL4882745

SCHEMBL4882745

O=Cc1ccc(S(=O)(=O)O)cc1S(=O)(=O)O.[NaH].[NaH]

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.40
HSD17B10 Q99714 4/20 0.40
SENP3 Q9H4L4 2/20 0.40
SENP2 Q9HC62 2/20 0.40
SENP1 Q9P0U3 2/20 0.40
SUMO2 P61956 1/20 0.40
SUMO1 P63165 1/20 0.40
SENP7 Q9BQF6 1/20 0.40
CYP2C19 P33261 2/20 0.40
CYP2C9 P11712 1/20 0.40
CASP6 P55212 1/20 0.40
RAD1 O60671 1/20 0.39
P2RY6 Q15077 1/20 0.39
LMNA P02545 1/20 0.39
TDP1 Q9NUW8 3/20 0.38
TIMP3 P35625 1/20 0.38
TSHR P16473 3/20 0.38
NT5E P21589 1/20 0.38
KDM4E B2RXH2 2/20 0.37
HPGD P15428 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
SCHEMBL2996002 1.00 ALDH1A1 (0.40) ALDH1A1HSD17B10SENP3SENP2SENP1
SCHEMBL225048 0.98 ALDH1A1 (0.41) ALDH1A1HSD17B10SENP3SENP2SENP1
SCHEMBL29396279 0.98 ALDH1A1 (0.41) ALDH1A1HSD17B10SENP3SENP2SENP1
Water SCHEMBL4381911 0.96 ALDH1A1 (0.41) ALDH1A1HSD17B10SENP3SENP2SENP1
SCHEMBL19718140 0.85 ALDH1A1 (0.40) ALDH1A1HSD17B10SENP3SENP2SENP1
SCHEMBL867590 0.85 ALDH1A1 (0.40) ALDH1A1HSD17B10SENP3SENP2SENP1
SCHEMBL28565819 0.84 ALDH1A1 (0.42) ALDH1A1HSD17B10CYP2C19CYP2C9CASP6
SCHEMBL11327900 0.84 LMNA (0.39) ALDH1A1SENP3SENP2SENP1SUMO2
SCHEMBL3789574 0.83 TDP1 (0.50) ALDH1A1HSD17B10SENP3SENP2SENP1
SCHEMBL867464 0.82 ALDH1A1 (0.41) ALDH1A1HSD17B10SENP3SENP2SENP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114539451-B Hydroxyl-rich single-ion conductor polymer SPVA-Li and preparation method and application thereof 中国地质大学(武汉) 2022-11-08 CN claimed
CN-114539451-A Hydroxyl-rich single-ion conductor polymer SPVA-Li and preparation method and application thereof 中国地质大学(武汉) 2022-05-27 CN claimed
WO-2016130687-A1 SYSTEMS AND METHODS FOR IMPROVING PERFORMANCE OF OSMOTICALLY DRIVEN MEMBRANE SYSTEMS OASYS WATER, INC. (US) 2016-08-18 WO claimed
US-20160158705-A1 SYSTEMS AND METHODS FOR IMPROVING PERFORMANCE OF OSMOTICALLY DRIVEN MEMBRANE SYSTEMS CHINA CAMC ENGINEERING HONGKONG CO., LIMITED (HK) 2016-06-09 US claimed
US-20240343845-A1 DISPERSION STABILIZER AND METHOD FOR PRODUCING VINYL-BASED POLYMER JAPAN VAM & POVAL CO., LTD. (JP) 2024-10-17 US disclosed
WO-2024203772-A1 METHOD FOR PRODUCING ALPHA-CYANOACRYLATE 東亞合成株式会社 2024-10-03 WO disclosed
WO-2024202448-A1 BIOLOGICAL COMPONENT CONCENTRATION MEASUREMENT REAGENT, MEASUREMENT METHOD, AND SENSOR テルモ株式会社 2024-10-03 WO disclosed
EP-4428532-A1 BIOLOGICAL COMPONENT CONCENTRATION MEASUREMENT REAGENT, MEASUREMENT METHOD, AND SENSOR Terumo Kabushiki Kaisha (JP) 2024-09-11 EP disclosed
WO-2024150650-A1 POLYVINYL ALCOHOL POLYMER AND METHOD FOR PRODUCING THE SAME 日本酢ビ・ポバール株式会社 2024-07-18 WO disclosed
WO-2024143249-A1 POLYVINYL ALCOHOL POLYMER, DISPERSION STABILIZER, AND METHOD FOR PRODUCING VINYL POLYMER 日本酢ビ・ポバール株式会社 2024-07-04 WO disclosed
WO-2024143250-A1 POLYVINYL ALCOHOL POLYMER, DISPERSION STABILIZER AND METHOD FOR PRODUCING VINYL POLYMER 日本酢ビ・ポバール株式会社 2024-07-04 WO disclosed
US-20240167922-A1 TRANSPARENTIZING REAGENT AND TRANSPARENTIZING METHOD KYOTO UNIVERSITY (JP) 2024-05-23 US disclosed
US-6339147-B1 OLIGONUCLEOTIDES JOINED TO SOLID SUPPORTS EPOCH BIOSCIENCES, INC. 2002-01-15 US disclosed
WO-2001089507-A1 NOVEL FORMULATIONS OF α-2,4-DISULFOPHENYL-N-TERT-BUTYLNITRONE ASTRAZENECA AB (SE) 2001-11-29 WO disclosed
WO-2001051461-A1 NOVEL PROCESS FOR THE PREPARATION OF α-(2-4-DISULFOPHENYL)-N-TERT-BUTYLNITRONE AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF ASTRAZENECA AB (SE) 2001-07-19 WO disclosed
WO-2001051460-A1 NOVEL PROCESS FOR THE PREPARATION OF α-(2-4-DISULFOPHENYL)-N-TERT-BUTYLNITRONE AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF ASTRAZENECA AB (SE) 2001-07-19 WO disclosed
WO-1992007975-A1 PROCESS FOR THE GALVANIC PRODUCTION OF A SMOOTH, NON-POROUS COATING IN THE MICROMETRE RANGE OF A PALLADIUM ALLOY OF DEFINED COMPOSITION ALLMENDINGER THOMAS (CH) 1992-05-14 WO disclosed
US-5035985-A Containing hydrophilic colloid layer with a specified dye FUJI PHOTO FILM CO., LTD. (JP) 1991-07-30 US disclosed
US-4833246-A PHOTOGRAPHY, FILTERS, OXONAL DYES FUJI PHOTO FILM CO., LTD. (JP) 1989-05-23 US disclosed
US-4715995-A Process for the preparation of alkali metal and alkaline earth salts of benzaldehyde-2,4-disulfonic acid HOECHST AKTIENGESELLSCHAFT (DE) 1987-12-29 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-20240167922-A1 TRANSPARENTIZING REAGENT AND TRANSPARENTIZING METHOD TST, TTR, ALB ALDH1A1 3942/4885HSD17B10 2184/4885SENP3 2376/4885

“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.