SCHEMBL6162025

SCHEMBL6162025

O=S(=O)(Cl)c1ccc2c(c1)Cc1ccccc1-2

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 4/20 0.54
ALDH1A1 P00352 4/20 0.54
LMNA P02545 4/20 0.54
NPSR1 Q6W5P4 2/20 0.54
GAA P10253 2/20 0.54
MAPT P10636 5/20 0.50
SMN1; SMN2 Q16637 4/20 0.50
KMT2A Q03164 4/20 0.50
HPGD P15428 3/20 0.50
MEN1 O00255 3/20 0.50
HSD17B10 Q99714 3/20 0.50
USP2 O75604 2/20 0.50
HTT P42858 2/20 0.50
TDP1 Q9NUW8 2/20 0.50
CASP6 P55212 1/20 0.50
GFER P55789 1/20 0.50
POLB P06746 1/20 0.50
NPC1 O15118 1/20 0.50
RAB9A P51151 1/20 0.50
CA12 O43570 1/20 0.49

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
SCHEMBL2264797 0.91 KMT2A (0.58) KDM4EALDH1A1LMNANPSR1GAA
SCHEMBL13183878 0.82 KDM4E (0.54) KDM4EALDH1A1LMNANPSR1GAA
Potassium Ion SCHEMBL10575064 0.82 KDM4E (0.54) KDM4EALDH1A1LMNANPSR1GAA
SCHEMBL29755360 0.82 KDM4E (0.54) KDM4EALDH1A1LMNANPSR1GAA
SCHEMBL15851432 0.82 KDM4E (0.57) KDM4EALDH1A1LMNANPSR1GAA
Potassium SCHEMBL10575068 0.81 KDM4E (0.56) KDM4EALDH1A1LMNANPSR1GAA
SCHEMBL9780205 0.81 KMT2A (0.49) KDM4EALDH1A1LMNANPSR1GAA
Fluorene SCHEMBL4327570 0.80 MAOA (0.65) KDM4EALDH1A1LMNANPSR1GAA
SCHEMBL18184514 0.79 KDM4E (0.55) KDM4EALDH1A1LMNANPSR1GAA
SCHEMBL20364684 0.78 KDM4E (0.50) KDM4EALDH1A1LMNANPSR1GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110658163-A Method for monitoring reaction in synthesis of DNA coding compound 成都先导药物开发股份有限公司 2020-01-07 CN claimed
CN-110658163-A Method for monitoring reaction in synthesis of DNA coding compound 成都先导药物开发股份有限公司 2020-01-07 CN disclosed
EP-1233017-B1 Tricyclic sulfonamides useful as matrix metalloproteinase inhibitors WARNER LAMBERT CO (US) 2005-12-14 EP disclosed
US-6906092-B2 Method of inhibiting matrix metalloproteinases WARNER-LAMBERT COMPANY (US) 2005-06-14 US disclosed
US-20040029945-A1 Method of inhibiting matrix metalloproteinases O'BRIEN PATRICK MICHAEL (US) 2004-02-12 US disclosed
US-6624177-B1 Treating diseases in which matrix melatoproteinases are involved such as multiple sclerosis, atherosclerotic plaque rupture, restenosis, aortic aneurism, heart failure, periodontal disease, corneal ulceration, burns, decubital WARNER-LAMBERT COMPANY 2003-09-23 US disclosed
US-6620835-B2 Sulfonamide-substituted benzothiophenes (that may be oxidized), carbazoles, fluorenes and fluorenones WARNER-LAMBERT COMPANY 2003-09-16 US disclosed
US-6559142-B2 Tricyclic substituted cyclic sulfonamides compound is useful for treating heart disease, multiple sclerosis, arthritis, atherosclerosis, and osteoporosis WARNER-LAMBERT COMPANY 2003-05-06 US disclosed
US-20030032665-A1 Method of inhibiting matrix metalloproteinases O'BRIEN PATRICK MICHAEL (US) 2003-02-13 US disclosed
US-20020169160-A1 Sulfonamide matrix metalloproteinase inhibitors O'BRIEN PATRICK MICHAEL (US) 2002-11-14 US disclosed
EP-1233017-A1 Tricyclic sulfonamides useful as matrix metalloproteinase inhibitors WARNER-LAMBERT COMPANY (US) 2002-08-21 EP disclosed
US-6294674-B1 FOR THERAPY OF MULTIPLE SCLEROSIS, ATHEROSCLEROTIC PLAQUE RUPTURE, RESTENOSIS, AORTIC ANEURISM, HEART FAILURE, PERIODONTAL DISEASE, CORNEAL ULCERATION, BURNS, DECUBITAL ULCERS, CHRONIC ULCERS OR WOUNDS, CANCER METASTASIS WARNER-LAMBERT COMPANY 2001-09-25 US disclosed
EP-0931045-A1 MATRIX METALLOPROTEINASE INHIBITORS AND THEIR THERAPEUTIC USES WARNER-LAMBERT COMPANY (US) 1999-07-28 EP disclosed
EP-0929542-A1 COMPOUNDS FOR AND A METHOD OF INHIBITING MATRIX METALLOPROTEINASES WARNER-LAMBERT COMPANY (US) 1999-07-21 EP disclosed
WO-1998009957-A1 COMPOUNDS FOR AND A METHOD OF INHIBITING MATRIX METALLOPROTEINASES WARNER-LAMBERT COMPANY (US) 1998-03-12 WO disclosed
WO-1998009934-A1 MATRIX METALLOPROTEINASE INHIBITORS AND THEIR THERAPEUTIC USES WARNER-LAMBERT COMPANY (US) 1998-03-12 WO disclosed
US-4857644-A Aryl sulfonopiperazines as anti-inflammatory agents AMERICAN HOME PRODUCTS CORPORATION (US) 1989-08-15 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 (3 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-20030032665-A1 Method of inhibiting matrix metalloproteinases MMP17, MMP1, MMP12 KDM4E 3386/4885ALDH1A1 387/4885LMNA 4322/4885
US-20040029945-A1 Method of inhibiting matrix metalloproteinases MMP17, MMP1, MMP12 KDM4E 3386/4885ALDH1A1 387/4885LMNA 4322/4885
US-20020169160-A1 Sulfonamide matrix metalloproteinase inhibitors MMP9, MMP10, MMP3 KDM4E 1309/4885ALDH1A1 1386/4885LMNA 2607/4885

“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.