SCHEMBL8020201

SCHEMBL8020201

COC(=O)[C@H]1C(=O)CC[C@@H]1C(=O)OC

nearest known ligand 0.43

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.43
HIF1A Q16665 1/20 0.43
CHRM2 P08172 1/20 0.40
CHRM4 P08173 1/20 0.40
CHRM3 P20309 1/20 0.40
ALDH1A1 P00352 1/20 0.39
TSHR P16473 1/20 0.38
HTT P42858 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
BRD4 O60885 1/20 0.34
KMT2A Q03164 1/20 0.34
KDM4E B2RXH2 1/20 0.34
HSD17B10 Q99714 1/20 0.34
SLC6A2 P23975 1/20 0.33

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
SCHEMBL7718731 1.00 CYP1A2 (0.43) CYP1A2HIF1ACHRM2CHRM4CHRM3
SCHEMBL8020205 1.00 CYP1A2 (0.43) CYP1A2HIF1ACHRM2CHRM4CHRM3
SCHEMBL7199227 0.90 CYP1A2 (0.42) CYP1A2HIF1ACHRM2CHRM4CHRM3
SCHEMBL3974808 0.89 CYP1A2 (0.41) CYP1A2HIF1ACHRM2CHRM4CHRM3
SCHEMBL8999992 0.89 CYP1A2 (0.45) CYP1A2HIF1ACHRM2CHRM4CHRM3
SCHEMBL8999987 0.89 CYP1A2 (0.45) CYP1A2HIF1ACHRM2CHRM4CHRM3
SCHEMBL9000000 0.89 CYP1A2 (0.45) CYP1A2HIF1ACHRM2CHRM4CHRM3
SCHEMBL10951734 0.81 ALDH1A1 (0.35) CYP1A2HIF1ACHRM2CHRM4CHRM3
SCHEMBL3301366 0.81 CYP1A2 (0.46) CYP1A2HIF1AALDH1A1BRD4KMT2A
SCHEMBL5215776 0.80 CHRM2 (0.40) CYP1A2HIF1ACHRM2CHRM4CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4125556-A Synthesis of 11-deoxyprostaglandins THE DOW CHEMICAL COMPANY (US) 1978-11-14 US claimed
US-6114364-A 2-((SUBSTITUTED)ALKYL(THIO, SULFONYL, OR SULFOXY)METHYL), 3-(CARBOXYL OR ALIPHATIC HYDROCARBONYL)CYCLOPENTAN-1-ONE DERIVATIVES, EXCEPT CYSTACYCLIN; USE AS NEURON DIFFERENTIATION ACCELERATOR NIPPON KAYAKU CO., LTD. (JP) 2000-09-05 US disclosed
EP-0976709-A1 2,3-DISUBSTITUTED CYCLOPENTANONE DERIVATIVES, PROCESS FOR PRODUCING THE SAME, AND MEDICINAL USE THEREOF NIPPON KAYAKU CO., LTD. (JP) 2000-02-02 EP disclosed
US-4532081-A 2-(6'-cyano-2'-hexynyl)-2-(b,b,b -trichlorocarboethoxy)-3-carbomethoxy cyclopentanone THE DOW CHEMICAL COMPANY (US) 1985-07-30 US disclosed
US-4532081-A 2-(6'-cyano-2'-hexynyl)-2-(b,b,b -trichlorocarboethoxy)-3-carbomethoxy cyclopentanone THE DOW CHEMICAL COMPANY (US) 1985-07-30 US disclosed
US-4447636-A TRANS-2-B,B,B-TRICHLOROCARBOETHOXY-3 -CARBOMETHOXYCYCLOPENTANONE INTERMEDIATE THE DOW CHEMICAL COMPANY (US) 1984-05-08 US disclosed
US-4447636-A TRANS-2-B,B,B-TRICHLOROCARBOETHOXY-3 -CARBOMETHOXYCYCLOPENTANONE INTERMEDIATE THE DOW CHEMICAL COMPANY (US) 1984-05-08 US disclosed
US-4146553-A Intermediates for synthesizing 11-deoxyprostaglandins THE DOW CHEMICAL COMPANY (US) 1979-03-27 US disclosed
US-4146553-A Intermediates for synthesizing 11-deoxyprostaglandins THE DOW CHEMICAL COMPANY (US) 1979-03-27 US disclosed
US-4125556-A Synthesis of 11-deoxyprostaglandins THE DOW CHEMICAL COMPANY (US) 1978-11-14 US disclosed
US-4125556-A Synthesis of 11-deoxyprostaglandins THE DOW CHEMICAL COMPANY (US) 1978-11-14 US disclosed