SCHEMBL4936620

SCHEMBL4936620

CC(C)OS(=O)(=O)Cc1ccccc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.55
HPGD P15428 1/20 0.49
CA1 P00915 2/20 0.47
CA2 P00918 2/20 0.47
PRSS1 P07477 2/20 0.47
PRSS2 P07478 2/20 0.47
PRSS3 P35030 2/20 0.47
FAAH O00519 1/20 0.47
ELANE P08246 1/20 0.47
PRTN3 P24158 1/20 0.47
CA5A P35218 1/20 0.47
CA9 Q16790 1/20 0.47
HTT P42858 2/20 0.44
TSHR P16473 2/20 0.43
MEN1 O00255 2/20 0.42
ALDH1A1 P00352 2/20 0.42
MMP1 P03956 1/20 0.42
MMP2 P08253 1/20 0.42
MMP9 P14780 1/20 0.42
MMP8 P22894 1/20 0.42

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
SCHEMBL28357823 0.98 KMT2A (0.53) KMT2AHPGDCA1CA2PRSS1
SCHEMBL28041171 0.85 KMT2A (0.52) KMT2AHPGDCA1CA2PRSS1
SCHEMBL9040129 0.85 KMT2A (0.52) KMT2AHPGDCA1CA2PRSS1
SCHEMBL6916227 0.83 KMT2A (0.50) KMT2AHPGDCA1CA2PRSS1
SCHEMBL10950994 0.83 KMT2A (0.50) KMT2AHPGDCA1CA2PRSS1
SCHEMBL7068759 0.83 HPGD (0.48) KMT2AHPGDCA1CA2PRSS1
SCHEMBL10434708 0.82 KMT2A (0.49) KMT2AHPGDCA1CA2PRSS1
SCHEMBL7630233 0.82 KMT2A (0.49) KMT2AHPGDCA1CA2PRSS1
SCHEMBL28588753 0.81 TXNRD1 (0.39) KMT2AHPGDCA1CA2CA9
SCHEMBL6913132 0.80 KMT2A (0.47) KMT2AHPGDCA1CA2PRSS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0110252-B1 HEAT-SENSITIVE REGISTRATION MATERIAL BASF Aktiengesellschaft (DE) 1985-11-13 EP claimed
US-4523208-A SULFONIC ACID ESTER AS ACTIVATOR BASF AKTIENGESELLSCHAFT (DE) 1985-06-11 US claimed
US-4383126-A Preparation of monoalkyl ethers of hydroxyphenols BAYER AKTIENGESELLSCHAFT (DE) 1983-05-10 US claimed
CN-118688346-A Application of polymer modified silica gel adsorption material in analysis of sulfonate genotoxic impurities 山东大学 2024-09-24 CN disclosed
CN-109071960-B Silicon-containing heterocyclic matting agents, compounds and polymers 富士胶片和光纯药株式会社 2021-01-12 CN disclosed
CN-111218126-A Matting agent, compound and polymer 富士胶片和光纯药株式会社 2020-06-02 CN disclosed
CN-107001807-B Compound and polymer 富士胶片和光纯药株式会社 2020-04-03 CN disclosed
CN-108840793-A A kind of method that application simulation mobile bed chromatic prepares gamma-thujaplicin 辽宁科技大学 2018-11-20 CN disclosed
EP-2474536-B1 PROCESS FOR PREPARATION OF PYRIMIDINYLACETONITRILE DERIVATIVES AND INTERMEDIATES FOR SYNTHESIS THEREOF IHARA CHEMICAL IND CO (JP) 2014-06-25 EP disclosed
CN-102093257-B Method for preparing 2,2-diisopropylpropionitrile WENZHOU ZHONGTAI CHEMICAL CO LTD 2013-09-11 CN disclosed
US-20120178931-A1 PROCESS FOR PREPARATION OF PYRIMIDINYLACETONITRILE DERIVATIVES AND INTERMEDIATES FOR SYNTHESIS THEREOF IHARA CHEMICAL INDUSTRY CO., LTD (JP) 2012-07-12 US disclosed
EP-0387360-B1 CYANINE COMPOUNDS ASAHI CHEMICAL CO (JP) 1994-01-12 EP disclosed
US-5087704-A Infrared light absorbing dye for use in optical recording media or semiconductor laser recording ASAHI CHEMICAL CO., LTD. (JP) 1992-02-11 US disclosed
US-5055589-A Chemical intermediate for cyanine dyes ASAHI CHEMICAL CO., LTD. (JP) 1991-10-08 US disclosed
US-5023366-A Reacted with a benzyl halide, alcohol or ether; for pressure sensitive elements MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1991-06-11 US disclosed
US-5008401-A Cyanine compounds ASAHI CHEMICAL CO., LTD. (JP) 1991-04-16 US disclosed
EP-0387357-A1 INDOLENINE DERIVATIVES ASAHI CHEMICAL CO., LTD. (JP) 1990-09-19 EP disclosed
EP-0387360-A1 CYANINE COMPOUNDS ASAHI CHEMICAL CO., LTD. (JP) 1990-09-19 EP disclosed
US-4406905-A COMPLEXING, ANTIBIOTICS CIBA-GEIGY CORPORATION (US) 1983-09-27 US disclosed
US-4383126-A Preparation of monoalkyl ethers of hydroxyphenols BAYER AKTIENGESELLSCHAFT (DE) 1983-05-10 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-20120178931-A1 PROCESS FOR PREPARATION OF PYRIMIDINYLACETONITRILE DERIVATIVES AND INTERMEDIATES FOR SYNTHESIS THEREOF DPYD, UMPS, PNP KMT2A 1075/4885HPGD 405/4885CA1 4826/4885

“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.