SCHEMBL670176

SCHEMBL670176

Cc1ccc(S(=O)(=O)c2cc3ccccc3[nH]2)cc1

nearest known ligand 0.72

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 2/20 0.56
CNR1 P21554 2/20 0.54
KDM4E B2RXH2 5/20 0.50
AKR1B1 P15121 1/20 0.50
HSD17B10 Q99714 1/20 0.50
BRD4 O60885 1/20 0.49
EGFR P00533 1/20 0.48
SRC P12931 1/20 0.48
GAA P10253 2/20 0.47
ALDH1A1 P00352 3/20 0.44
NPSR1 Q6W5P4 2/20 0.44
RXFP1 Q9HBX9 1/20 0.44
MAPT P10636 1/20 0.44
PDGFRB P09619 1/20 0.44
PDGFRA P16234 1/20 0.44
CA12 O43570 1/20 0.44
CA1 P00915 1/20 0.44
CA9 Q16790 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
MEN1 O00255 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
SCHEMBL30684143 1.00 CA2 (0.56) CA2CNR1KDM4EAKR1B1HSD17B10
SCHEMBL31561597 0.86 CA2 (0.62) CA2CNR1KDM4EAKR1B1HSD17B10
SCHEMBL3237494 0.86 CA2 (0.62) CA2CNR1KDM4EAKR1B1HSD17B10
SCHEMBL4862702 0.84 CA2 (0.56) CA2CNR1AKR1B1MAPTCA12
SCHEMBL8960439 0.84 CA2 (0.56) CA2CNR1KDM4EAKR1B1HSD17B10
SCHEMBL13542579 0.83 CA2 (0.51) CA2CNR1KDM4EAKR1B1HSD17B10
SCHEMBL8120975 0.83 KDM4E (0.49) CA2CNR1KDM4ERXFP1PDGFRB
SCHEMBL28568569 0.82 CA2 (0.71) CA2CNR1KDM4EAKR1B1HSD17B10
SCHEMBL29520525 0.82 CA2 (0.57) CA2CNR1AKR1B1CA12CA1
SCHEMBL14502491 0.81 CA2 (0.53) CA2CNR1KDM4EAKR1B1BRD4

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120081778-A Central chiral sulfonyl indole and synthesis method thereof 南京理工大学 2025-06-03 CN disclosed
CN-112409236-B Method for synthesizing 3-thioether indole with high selectivity 上海应用技术大学 2022-10-14 CN disclosed
CN-108129440-B Method for synthesizing chiral chromene derivative 中国科学院大连化学物理研究所 2021-05-28 CN disclosed
CN-112409236-A Method for synthesizing 3-thioether indole with high selectivity 上海应用技术大学 2021-02-26 CN disclosed
CN-109438317-A A kind of preparation method of nitrogen-alkyl (deuteroalkyl) heteroaromatic and alkyl (deuteroalkyl) aryl ethers compounds 武汉大学 2019-03-08 CN disclosed
CN-106366032-A Applications of chiral organic alkali in preparation of chiral sulfur-containing indole compound in water-oil two-phase system 中国科学院大连化学物理研究所 2017-02-01 CN disclosed
US-9034895-B2 Composition and methods for treating glioblastoma UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR COMMERCIALIZATION (US) 2015-05-19 US disclosed
US-9034895-B2 Composition and methods for treating glioblastoma UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR COMMERCIALIZATION (US) 2015-05-19 US disclosed
US-9034895-B2 Composition and methods for treating glioblastoma UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR COMMERCIALIZATION (US) 2015-05-19 US disclosed
EP-2606032-B1 COMPOSITION AND METHODS FOR TREATING GLIOBLASTOMAS UNIV WASHINGTON CT COMMERCIALI (US) 2015-01-07 EP disclosed
EP-2606032-B1 COMPOSITION AND METHODS FOR TREATING GLIOBLASTOMAS UNIV WASHINGTON CT COMMERCIALI (US) 2015-01-07 EP disclosed
US-20130197026-A1 COMPOSITION AND METHODS FOR TREATING GLIOBLASTOMA Unversity of Washington Through its Center for Commercialization (US) 2013-08-01 US disclosed
US-20130197026-A1 COMPOSITION AND METHODS FOR TREATING GLIOBLASTOMA Unversity of Washington Through its Center for Commercialization (US) 2013-08-01 US disclosed
US-20130197026-A1 COMPOSITION AND METHODS FOR TREATING GLIOBLASTOMA Unversity of Washington Through its Center for Commercialization (US) 2013-08-01 US disclosed
EP-2606032-A2 COMPOSITION AND METHODS FOR TREATING GLIOBLASTOMA University Of Washington Through Its Center For Commercialization (US) 2013-06-26 EP disclosed
WO-2012024670-A2 COMPOSITION AND METHODS FOR TREATING GLIOBLASTOMA UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR COMMERCIALIZATION (US) 2012-02-23 WO disclosed
WO-2012024670-A2 COMPOSITION AND METHODS FOR TREATING GLIOBLASTOMA UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR COMMERCIALIZATION (US) 2012-02-23 WO disclosed
CN-1706802-A Prepn process of 2-ary lactate, naprosyn and ibuprofen SHANHAI INST OF ORGANIC CHEMIS (CN) 2005-12-14 CN 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-20130197026-A1 COMPOSITION AND METHODS FOR TREATING GLIOBLASTOMA MGMT, NEFM, TP53 CA2 1599/4885CNR1 2351/4885KDM4E 2429/4885

“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.