SCHEMBL9969986

SCHEMBL9969986

CC(C)Cn1nc2ccccc2n1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.44
SMN1; SMN2 Q16637 4/20 0.44
CNR1 P21554 1/20 0.44
CNR2 P34972 1/20 0.44
TRPV1 Q8NER1 1/20 0.44
TOP2A P11388 1/20 0.43
LMNA P02545 5/20 0.42
KDM4E B2RXH2 4/20 0.42
HTT P42858 3/20 0.42
L3MBTL1 Q9Y468 2/20 0.42
GAA P10253 2/20 0.42
NPC1 O15118 1/20 0.42
GLA P06280 1/20 0.42
RAB9A P51151 1/20 0.42
HPGD P15428 3/20 0.41
TSHR P16473 3/20 0.40
HSD17B10 Q99714 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
TLR7 Q9NYK1 2/20 0.39
PRKACA P17612 1/20 0.39

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
SCHEMBL7570582 0.83 LMNA (0.38) ALDH1A1SMN1; SMN2LMNAKDM4EHTT
SCHEMBL14944890 0.83 KDM4E (0.40) ALDH1A1SMN1; SMN2LMNAKDM4EHTT
SCHEMBL23046922 0.78 TSHR (0.51) ALDH1A1SMN1; SMN2LMNAKDM4EHTT
SCHEMBL818131 0.77 KDM4E (0.38) ALDH1A1SMN1; SMN2LMNAKDM4EHTT
SCHEMBL20872965 0.75 CSNK2A1 (0.53) ALDH1A1SMN1; SMN2LMNAKDM4EHTT
SCHEMBL16522427 0.74 TSHR (0.44) ALDH1A1SMN1; SMN2LMNAKDM4EHTT
SCHEMBL18040334 0.74 TRPV1 (0.45) ALDH1A1SMN1; SMN2CNR1CNR2TRPV1
SCHEMBL6229399 0.73 HTT (0.45) ALDH1A1SMN1; SMN2TOP2ALMNAKDM4E
SCHEMBL8745426 0.73 KDM4E (0.42) ALDH1A1LMNAKDM4EHTTL3MBTL1
SCHEMBL175462 0.72 CSNK2A1 (0.39) ALDH1A1SMN1; SMN2LMNAKDM4EHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119161374-A Light conversion agent, preparation method thereof, light conversion adhesive film and photovoltaic module 常州百佳年代薄膜科技股份有限公司 2024-12-20 CN claimed
WO-2025102541-A1 LIGHT CONVERSION AGENT HAVING ASYMMETRIC STRUCTURE, LIGHT CONVERSION ADHESIVE FILM AND PREPARATION METHOD THEREFOR 常州百佳年代薄膜科技股份有限公司 2025-05-22 WO disclosed
CN-119161374-A Light conversion agent, preparation method thereof, light conversion adhesive film and photovoltaic module 常州百佳年代薄膜科技股份有限公司 2024-12-20 CN disclosed
CN-118755401-A Metal corrosion inhibition packaging adhesive film, preparation method, application method and photovoltaic module packaging assembly 广州市黑本新材料科技有限公司 2024-10-11 CN disclosed
CN-117247362-B Light conversion agent with asymmetric structure, light conversion adhesive film and preparation method thereof 常州百佳年代薄膜科技股份有限公司 2024-02-13 CN disclosed
CN-117247362-A Light conversion agent with asymmetric structure, light conversion adhesive film and preparation method thereof 常州百佳年代薄膜科技股份有限公司 2023-12-19 CN disclosed
US-10840397-B2 Highly-fluorescent and photo-stable chromophores for wavelength conversion NITTO DENKO CORPORATION (JP) 2020-11-17 US disclosed
US-10840397-B2 Highly-fluorescent and photo-stable chromophores for wavelength conversion NITTO DENKO CORPORATION (JP) 2020-11-17 US disclosed
CN-105209936-B Optical element for correcting color blindness 日东电工株式会社 2020-01-14 CN disclosed
US-10461201-B2 Highly-fluorescent and photo-stable chromophores for wavelength conversion NITTO DENKO CORPORATION (JP) 2019-10-29 US disclosed
US-8431597-B2 Benzimidazole derivatives PFIZER INC. (US) 2013-04-30 US disclosed
WO-2013049062-A2 HIGHLY-FLUORESCENT AND PHOTO-STABLE CHROMOPHORES FOR ENHANCED SOLAR HARVESTING EFFICIENCY NITTO DENKO CORPORATION (JP) 2013-04-04 WO disclosed
WO-2013049062-A2 HIGHLY-FLUORESCENT AND PHOTO-STABLE CHROMOPHORES FOR ENHANCED SOLAR HARVESTING EFFICIENCY NITTO DENKO CORPORATION (JP) 2013-04-04 WO disclosed
US-20130074927-A1 HIGHLY-FLUORESCENT AND PHOTO-STABLE CHROMOPHORES FOR ENHANCED SOLAR HARVESTING EFFICIENCY NITTO DENKO CORPORATION (JP) 2013-03-28 US disclosed
US-20130074927-A1 HIGHLY-FLUORESCENT AND PHOTO-STABLE CHROMOPHORES FOR ENHANCED SOLAR HARVESTING EFFICIENCY NITTO DENKO CORPORATION (JP) 2013-03-28 US disclosed
US-20130074927-A1 HIGHLY-FLUORESCENT AND PHOTO-STABLE CHROMOPHORES FOR ENHANCED SOLAR HARVESTING EFFICIENCY NITTO DENKO CORPORATION (JP) 2013-03-28 US disclosed
US-20120157495-A1 BENZIMIDAZOLE DERIVATIVES PFIZER INC. 2012-06-21 US disclosed
US-8148401-B2 Benzimidazole derivatives PFIZER INC. (US) 2012-04-03 US disclosed
US-20110028461-A1 HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS MERCK SHARP & DOHME LLC 2011-02-03 US disclosed
US-20090005416-A1 BENZIMIDAZOLE DERIVATIVES PFIZER INC. 2009-01-01 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 (4 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-20090005416-A1 BENZIMIDAZOLE DERIVATIVES BOD1L1, H1-3, BRIX1 ALDH1A1 1240/4885SMN1; SMN2 1764/4885CNR1 2942/4885
US-20120157495-A1 BENZIMIDAZOLE DERIVATIVES BOD1L1, H1-3, BRIX1 ALDH1A1 1240/4885SMN1; SMN2 1764/4885CNR1 2942/4885
US-20130074927-A1 HIGHLY-FLUORESCENT AND PHOTO-STABLE CHROMOPHORES FOR ENHANCED SOLAR HARVESTING EFFICIENCY SUN2, NES, CRY1 ALDH1A1 1484/4885SMN1; SMN2 2766/4885CNR1 911/4885
US-20110028461-A1 HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS ADRB3, ADRB1, ADRB2 ALDH1A1 352/4885SMN1; SMN2 3396/4885CNR1 62/4885

“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.