SCHEMBL2464667

SCHEMBL2464667

N#Cc1[nH]c2ccccc2c1C#N

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE9A O76083 6/20 0.49
ALDH1A1 P00352 4/20 0.46
GPR3 P46089 1/20 0.46
HSD17B10 Q99714 1/20 0.46
DRD2 P14416 1/20 0.44
DRD4 P21917 1/20 0.44
DRD3 P35462 1/20 0.44
PDE1C Q14123 1/20 0.44
KDM4E B2RXH2 3/20 0.43
KMT2A Q03164 2/20 0.43
GAA P10253 2/20 0.43
MEN1 O00255 1/20 0.43
MAPT P10636 1/20 0.43
CACNA1B Q00975 1/20 0.43
APBA1 Q02410 1/20 0.43
EGFR P00533 2/20 0.43
SRC P12931 1/20 0.43
GABRP O00591 1/20 0.43
GABRD O14764 1/20 0.43
GABRA1 P14867 1/20 0.43

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
SCHEMBL29635217 1.00 PDE9A (0.49) PDE9AALDH1A1GPR3HSD17B10DRD2
SCHEMBL3676401 0.79 AHR (0.57) PDE9AALDH1A1GPR3HSD17B10PDE1C
SCHEMBL16156592 0.78 ALDH1A1 (0.44) PDE9AALDH1A1GPR3HSD17B10DRD2
SCHEMBL8588245 0.78 ALDH1A1 (0.50) ALDH1A1GPR3HSD17B10DRD2DRD4
SCHEMBL20505152 0.78 ALDH1A1 (0.44) PDE9AALDH1A1GPR3HSD17B10DRD2
SCHEMBL9034264 0.78 ALDH1A1 (0.44) PDE9AALDH1A1GPR3HSD17B10DRD2
SCHEMBL2731190 0.78 DRD2 (0.47) PDE9AALDH1A1GPR3HSD17B10DRD2
SCHEMBL3680016 0.78 AHR (0.55) PDE9AALDH1A1GPR3HSD17B10DRD2
SCHEMBL1514832 0.78 PDE9A (0.47) PDE9AALDH1A1GPR3HSD17B10PDE1C
SCHEMBL5858501 0.78 PLA2G1B (0.59) PDE9AALDH1A1GPR3HSD17B10PDE1C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114671880-B Synthesis and application of indole-2, 3-dinitrile antitumor compounds containing fatty amino 大连理工大学 2023-06-06 CN claimed
CN-114671880-A Synthesis and application of indole-2, 3-dinitrile antitumor compound containing aliphatic amino 大连理工大学 2022-06-28 CN claimed
CN-114671880-B Synthesis and application of indole-2, 3-dinitrile antitumor compounds containing fatty amino 大连理工大学 2023-06-06 CN disclosed
CN-114671880-B Synthesis and application of indole-2, 3-dinitrile antitumor compounds containing fatty amino 大连理工大学 2023-06-06 CN disclosed
CN-114671880-B Synthesis and application of indole-2, 3-dinitrile antitumor compounds containing fatty amino 大连理工大学 2023-06-06 CN disclosed
CN-114671880-A Synthesis and application of indole-2, 3-dinitrile antitumor compound containing aliphatic amino 大连理工大学 2022-06-28 CN disclosed
CN-114671880-A Synthesis and application of indole-2, 3-dinitrile antitumor compound containing aliphatic amino 大连理工大学 2022-06-28 CN disclosed
CN-114671880-A Synthesis and application of indole-2, 3-dinitrile antitumor compound containing aliphatic amino 大连理工大学 2022-06-28 CN disclosed
CN-110635167-B Nonaqueous electrolyte solution, battery containing same, and electric vehicle 比亚迪股份有限公司 2021-04-20 CN disclosed
CN-110635167-A Nonaqueous electrolyte solution, battery containing same, and electric vehicle 比亚迪股份有限公司 2019-12-31 CN disclosed
CN-110483555-A D (π-A) of the one kind based on pyrazine indoles end receptor2Type small molecule donor material and preparation method and application UNIV CHANGZHOU 2019-11-22 CN disclosed
US-8673948-B2 Chemical compounds GlaxoSmithKline, LLC (US) 2014-03-18 US disclosed
EP-2079466-B1 SUBSTITUTED INDOLE COMPOUNDS GLAXOSMITHKLINE LLC (US) 2014-01-15 EP disclosed
US-20110301203-A1 CHEMICAL COMPOUNDS GLAXOSMITHKLINE LLC (US) 2011-12-08 US disclosed
US-8026262-B2 Chemical compounds GLAXOSMITHKLINE LLC (US) 2011-09-27 US disclosed
US-20090264482-A1 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2009-10-22 US disclosed
US-7572820-B2 3-(2-methyl-4-(trifluoromethyl)-5-cyano-indol-1-yl-methyl)-5-(3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole or salt thereof; hypogonadism, sarcopenia, osteoporosis, wasting diseases, cancer cachexia, frailty, prostatic hyperplasia, prostate cancer, breast cancer; selective androgen receptor modulators SMITHKLINE BEECHAM CORPORATION (US) 2009-08-11 US disclosed
EP-2079466-A2 SUBSTITUTED INDOLE COMPOUNDS SmithKline Beecham Corporation (US) 2009-07-22 EP disclosed
US-20080139631-A1 3-(2-methyl-4-(trifluoromethyl)-5-cyano-indol-1-yl-methyl)-5-(3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole or salt thereof; hypogonadism, sarcopenia, osteoporosis, wasting diseases, cancer cachexia, frailty, prostatic hyperplasia, prostate cancer, breast cancer; selective androgen receptor modulators SMITHKLINE BEECHAM CORPORATION (US) 2008-06-12 US disclosed
WO-2008042571-A2 SUBSTITUTED INDOLE COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2008-04-10 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 (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-20090264482-A1 CHEMICAL COMPOUNDS AR, NR5A1, ESRRA PDE9A 1725/4885ALDH1A1 671/4885GPR3 173/4885
US-20110301203-A1 CHEMICAL COMPOUNDS AR, NR5A1, ESRRA PDE9A 1725/4885ALDH1A1 671/4885GPR3 173/4885
US-20080139631-A1 3-(2-methyl-4-(trifluoromethyl)-5-cyano-indol-1-yl-methyl)-5-(3-(trifluoromethyl)phenyl)-1,2,4-oxadiazole or salt thereof; hypogonadism, sarcopenia, osteoporosis, wasting diseases, cancer cachexia, frailty, prostatic hyperplasia, prostate cancer, breast cancer; selective androgen receptor modulators AR, NR5A1, NR3C2 PDE9A 2254/4885ALDH1A1 3006/4885GPR3 35/4885

“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.