SCHEMBL1726232

SCHEMBL1726232

CCCCCNC1=NCCO1

nearest known ligand 0.43

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ SMN1; SMN2 Q16637 1/20 0.43
▸ ADRA2A P08913 5/20 0.42
▸ ADRA2B P18089 5/20 0.42
▸ ADRA2C P18825 5/20 0.42
▸ ADRA1A P35348 3/20 0.42
▸ GMNN O75496 1/20 0.37
▸ CYP1A2 P05177 1/20 0.37
▸ CYP3A4 P08684 1/20 0.37
▸ HTR1A P08908 1/20 0.37
▸ CYP2D6 P10635 1/20 0.37
▸ CYP2C9 P11712 1/20 0.37
▸ TSHR P16473 1/20 0.37
▸ OPRK1 P41145 1/20 0.37
▸ HIF1A Q16665 1/20 0.37
▸ NISCH Q9Y2I1 1/20 0.37
▸ DNM2 P50570 3/20 0.34

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
SCHEMBL8707780 0.98 SMN1; SMN2 (0.42) SMN1; SMN2ADRA2AADRA2BADRA2CADRA1A
SCHEMBL11123645 0.98 SMN1; SMN2 (0.42) SMN1; SMN2ADRA2AADRA2BADRA2CADRA1A
SCHEMBL11123146 0.98 SMN1; SMN2 (0.42) SMN1; SMN2ADRA2AADRA2BADRA2CADRA1A
SCHEMBL11125149 0.94 SMN1; SMN2 (0.49) SMN1; SMN2ADRA2AADRA2BADRA2CADRA1A
SCHEMBL11121805 0.89 SMN1; SMN2 (0.41) SMN1; SMN2ADRA2AADRA2BADRA2CADRA1A
SCHEMBL9558829 0.88 ADRA2A (0.46) SMN1; SMN2ADRA2AADRA2BADRA2CADRA1A
SCHEMBL11123565 0.88 SMN1; SMN2 (0.40) SMN1; SMN2ADRA2AADRA2BADRA2CADRA1A
SCHEMBL11127867 0.88 SMN1; SMN2 (0.40) SMN1; SMN2ADRA2AADRA2BADRA2CADRA1A
SCHEMBL11123731 0.88 SMN1; SMN2 (0.40) SMN1; SMN2ADRA2AADRA2BADRA2CADRA1A
SCHEMBL11125378 0.86 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8178567-B2 Insecticidal substituted amino heterocyclic and heteroaryl derivatives FMC CORPORATION (US) 2012-05-15 — — US disclosed
EP-1960369-B1 INDANYL-AND TETRAHYDRONAPHTHYL-AMINO-AZOLINE COMPOUNDS FOR COMBATING ANIMAL PESTS BASF SE (DE) 2012-01-11 — — EP disclosed
US-7981437-B2 Indanyl- and tetrahydronaphthyl-amino-azoline compounds for combating animal pests BASF SE (DE) 2011-07-19 — — US disclosed
US-20100137385-A1 Insecticidal Substituted Amino Heterocyclic and Heteroaryl Derivatives BAYER CROPSCIENCE AG (DE) 2010-06-03 — — US disclosed
CN-101316824-A Indanyl-and tetrahydronaphthyl-amino-azoline compounds for combating animal pests BASF SE (DE) 2008-12-03 — — CN disclosed
US-20080293569-A1 Indanyl- and Tetrahydronaphthyl-Amino-Azoline Compounds for Combating Animal Pests BASF SE (DE) 2008-11-27 — — US disclosed
EP-1986498-A2 INSECTICIDAL SUBSTITUTED AMINO HETEROCYCLIC AND HETEROARYL DERIVATIVES Bayer CropScience AG (DE) 2008-11-05 — — EP disclosed
EP-1960369-A1 INDANYL-AND TETRAHYDRONAPHTHYL-AMINO-AZOLINE COMPOUNDS FOR COMBATING ANIMAL PESTS BASF SE (DE) 2008-08-27 — — EP disclosed
WO-2007093292-A2 INSECTICIDAL SUBSTITUTED AMINO HETEROCYCLIC AND HETEROARYL DERIVATIVES BAYER CROPSCIENCE AG (DE) 2007-08-23 — — WO disclosed
WO-2007060121-A1 INDANYL-AND TETRAHYDRONAPHTHYL-AMINO-AZOLINE COMPOUNDS FOR COMBATING ANIMAL PESTS BASF SE (DE) 2007-05-31 — — WO disclosed
EP-0724439-A1 USE OF 2-(2-ALKYLPHENYLAMINO)-OXAZOLINES, -THIAZOLINES AND -IMIDAZOLINES AS ALPHA 2 ADRENERGIC AGENTS Allergan (US) 1996-08-07 — — EP disclosed
EP-0420606-B1 Use of 2-cycloalkylamino oxazolines for reducing or maintaining intraocular pressure ALLERGAN INC (US) 1996-03-20 — — EP disclosed
WO-1996001813-A1 CONFORMATIONALLY RIGID BICYCLIC AND ADAMANTANE DERIVATIVES USEFUL AS α2-ADRENERGIC BLOCKING AGENTS ALLERGAN (US) 1996-01-25 — — WO disclosed
WO-1995011021-A1 USE OF 2-(2-ALKYLPHENYLAMINO)-OXAZOLINES, -THIAZOLINES AND -IMIDAZOLINES AS ALPHA 2 ADRENERGIC AGENTS ALLERGAN (US) 1995-04-27 — — WO disclosed
US-5252595-A Method for reducing or maintaining intraocular pressure in the mammalian eye by administering pharmaceutical compositions containing 2-(2-alkylphenylamino)-oxazolines, 2-(2-alkylphenylamino)-thiazolines and 2-(2-alkylphenylamino)-imidazolines ALLERGAN, INC. (US) 1993-10-12 — — US disclosed
US-5151440-A Treatment of glaucoma ALLERGAN, INC. (US) 1992-09-29 — — US disclosed
US-5066664-A Control of intraocular bleeding and pressure ALLERGAN, INC. (US) 1991-11-19 — — US disclosed
EP-0030350-B1 METHOD FOR REDUCING THE TERMINAL CARBOXYL GROUP CONTENT OF A SATURATED POLYESTER, A SATURATED POLYESTER HAVING A REDUCED TERMINAL CARBOXYL GROUP CONTENT, AND A MOLDED ARTICLE COMPOSED OF SUCH A SATURATED POLYESTER TEIJIN LIMITED (JP) 1984-10-10 — — EP disclosed
US-4351936-A COMPRISING ENDCAPPING WITH AN OXAZOLINE OR OXAZINE TEIJIN LIMITED (JP) 1982-09-28 — — US disclosed
EP-0030350-A1 Method for reducing the terminal carboxyl group content of a saturated polyester, a saturated polyester having a reduced terminal carboxyl group content, and a molded article composed of such a saturated polyester TEIJIN LIMITED (JP) 1981-06-17 — — EP 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 (2 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-20100137385-A1 Insecticidal Substituted Amino Heterocyclic and Heteroaryl Derivatives DDT, AAAS, DDC SMN1; SMN2 3097/4885ADRA2A 194/4885ADRA2B 118/4885
US-20080293569-A1 Indanyl- and Tetrahydronaphthyl-Amino-Azoline Compounds for Combating Animal Pests INMT, AIPL1, AADAT SMN1; SMN2 4403/4885ADRA2A 1392/4885ADRA2B 875/4885

“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.

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