SCHEMBL7140779

SCHEMBL7140779

Cc1ccc(S(=O)(=O)O)cc1.NCC(=O)COCc1ccccc1

nearest known ligand 0.47

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.47
CYP1A2 P05177 2/20 0.44
MAPT P10636 2/20 0.44
CYP2C9 P11712 1/20 0.44
NPC1 O15118 2/20 0.43
RAB9A P51151 1/20 0.43
CYP2D6 P10635 1/20 0.42
MAPK1 P28482 1/20 0.42
ALDH1A1 P00352 3/20 0.41
GAA P10253 2/20 0.41
PKM P14618 2/20 0.41
AR P10275 1/20 0.41
KMT2A Q03164 1/20 0.40
CA1 P00915 1/20 0.40
CA2 P00918 1/20 0.40
BCHE P06276 1/20 0.40
ACHE P22303 1/20 0.40
CA12 O43570 1/20 0.40
CYP3A4 P08684 1/20 0.40
ATM Q13315 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
Glycine SCHEMBL6374478 0.88 LMNA (0.50) LMNACYP1A2MAPTCYP2C9NPC1
SCHEMBL5136455 0.85 LMNA (0.54) LMNACYP1A2MAPTCYP2D6MAPK1
SCHEMBL4611094 0.83 ALDH1A1 (0.48) LMNACYP1A2MAPTCYP2C9CYP2D6
SCHEMBL57630 0.82 LMNA (0.62) LMNACYP1A2MAPTCYP2C9CYP2D6
SCHEMBL1177430 0.81 LMNA (0.62) LMNACYP1A2MAPTCYP2C9MAPK1
SCHEMBL7133879 0.79 ALDH1A1 (0.44) LMNACYP1A2MAPTCYP2C9NPC1
SCHEMBL20489941 0.79 CA1 (0.51) LMNACYP1A2MAPTCYP2C9CYP2D6
SCHEMBL717926 0.78 LMNA (0.68) LMNACYP1A2MAPTCYP2C9CYP2D6
SCHEMBL18281078 0.78 LMNA (0.68) LMNACYP1A2MAPTCYP2C9CYP2D6
Hydrochloric Acid SCHEMBL28233816 0.78 CA1 (0.50) LMNACYP2D6MAPK1ALDH1A1GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030092634-A1 Novel compounds and compositions as protease inhibitors AXYS PHARMACEUTICALS, INC. 2003-05-15 US disclosed
US-6506733-B1 Which process comprises hydrogenating a compound of Formula 9: presence of a catalytic amount of 20% palladium hydroxide on carbon. AXYS PHARMACEUTICALS, INC. 2003-01-14 US disclosed
EP-1159260-A1 NOVEL COMPOUNDS AND COMPOSITIONS AS PROTEASE INHIBITORS AXYS PHARMACEUTICALS, INC. (US) 2001-12-05 EP disclosed
WO-2000055124-A2 NOVEL COMPOUNDS AND COMPOSITIONS AS PROTEASE INHIBITORS AXYS PHARMACEUTICALS, INC. (US) 2000-09-21 WO 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-20030092634-A1 Novel compounds and compositions as protease inhibitors SERPINB1, HPN, CTRL LMNA 2624/4885CYP1A2 3203/4885MAPT 1848/4885

“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.