SCHEMBL947879

SCHEMBL947879

C#Cc1ccc(CCCCCC)cc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 2/20 0.61
TSHR P16473 1/20 0.61
ESR1 P03372 2/20 0.57
ADRA2A P08913 2/20 0.57
ADORA3 P0DMS8 2/20 0.57
TACR2 P21452 2/20 0.57
SLC6A2 P23975 2/20 0.57
SLC6A4 P31645 2/20 0.57
SLC6A3 Q01959 2/20 0.57
ALDH1A1 P00352 2/20 0.57
KDM4E B2RXH2 1/20 0.57
LMNA P02545 1/20 0.57
SHBG P04278 1/20 0.57
TP53 P04637 1/20 0.57
CYP3A4 P08684 1/20 0.57
HSPD1 P10809 1/20 0.57
ADRB3 P13945 1/20 0.57
HTR2C P28335 1/20 0.57
HSPE1 P61604 1/20 0.57
HIF1A Q16665 1/20 0.57

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
SCHEMBL4745509 1.00 HSD17B10 (0.61) HSD17B10TSHRESR1ADRA2AADORA3
SCHEMBL28243501 1.00 HSD17B10 (0.61) HSD17B10TSHRESR1ADRA2AADORA3
SCHEMBL28242843 1.00 HSD17B10 (0.61) HSD17B10TSHRESR1ADRA2AADORA3
SCHEMBL7794684 1.00 HSD17B10 (0.61) HSD17B10TSHRESR1ADRA2AADORA3
SCHEMBL177025 1.00 HSD17B10 (0.61) HSD17B10TSHRESR1ADRA2AADORA3
SCHEMBL948801 1.00 HSD17B10 (0.61) HSD17B10TSHRESR1ADRA2AADORA3
SCHEMBL31415597 1.00 HSD17B10 (0.61) HSD17B10TSHRESR1ADRA2AADORA3
SCHEMBL2773891 1.00 HSD17B10 (0.61) HSD17B10TSHRESR1ADRA2AADORA3
SCHEMBL170113 0.98 HSD17B10 (0.58) HSD17B10TSHRESR1ADRA2AADORA3
SCHEMBL10984815 0.94 HSD17B10 (0.70) HSD17B10TSHRESR1ADRA2AADORA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119633864-A Method for preparing thiophene compound by using one-pot method through double-function catalyst and catalyst used by same 浙江大学 2025-03-18 CN claimed
WO-2025049824-A1 FRAGRANCE AND FLAVOR COMPOSITIONS COMPRISING AROMATIC DERIVATIVES OSMO LABS, PBC (US) 2025-03-06 WO claimed
CN-117447295-A 1,3, 6-tris [2- (4-hexylphenyl) ethynyl ] pyrene and preparation method thereof 中国石油大学(华东) 2024-01-26 CN claimed
CN-115322644-B Modified alkynyl polymer coating constructed in situ at interface and preparation method and application thereof 中国科学院宁波材料技术与工程研究所 2023-06-02 CN claimed
CN-115650816-A Method for synthesizing 1, 3-diacetylene compound through heterogeneous catalysis 成都理工大学 2023-01-31 CN claimed
CN-115322644-A Modified alkynyl polymer coating constructed in situ at interface and preparation method and application thereof 中国科学院宁波材料技术与工程研究所 2022-11-11 CN claimed
CN-119661486-B Variable-temperature fluorescent sensing material with V-shaped structure pyrene dimer 中国石油大学(华东) 2026-05-15 CN disclosed
CN-119661486-A Variable-temperature fluorescent sensing material with V-shaped structure pyrene dimer 中国石油大学(华东) 2025-03-21 CN disclosed
CN-119633864-A Method for preparing thiophene compound by using one-pot method through double-function catalyst and catalyst used by same 浙江大学 2025-03-18 CN disclosed
WO-2025049824-A1 FRAGRANCE AND FLAVOR COMPOSITIONS COMPRISING AROMATIC DERIVATIVES OSMO LABS, PBC (US) 2025-03-06 WO disclosed
CN-118240209-A Be used for detecting Hg2+Condensed heterocyclic conjugated polymer and its synthesis method and application 陕西师范大学 2024-06-25 CN disclosed
CN-117447295-A 1,3, 6-tris [2- (4-hexylphenyl) ethynyl ] pyrene and preparation method thereof 中国石油大学(华东) 2024-01-26 CN disclosed
CN-117447295-A 1,3, 6-tris [2- (4-hexylphenyl) ethynyl ] pyrene and preparation method thereof 中国石油大学(华东) 2024-01-26 CN disclosed
EP-1274713-A1 ANTI-VIRAL PYRIMIDINE NUCLEOSIDE ANALOGUES University College Cardiff Consultants Limited (GB) 2003-01-15 EP disclosed
US-6417187-B2 PALLADIUM CATALYZED ARYLATION, ALKYLATION, DEIODINATION OR DEBROMINATION DOW AGROSCIENCES LLC 2002-07-09 US disclosed
WO-2002035580-A2 THREE-TERMINAL FIELD-CONTROLLED MOLECULAR DEVICES MOLECULAR ELECTRONICS CORPORATION (US) 2002-05-02 WO disclosed
US-20020019370-A1 Palladium catalyzed arylation, alkylation, deiodination or debromination DOW AGROSCIENCES LLC 2002-02-14 US disclosed
WO-2001083501-A1 ANTI-VIRAL PYRIMIDINE NUCLEOSIDE ANALOGUES UNIVERSITY COLLEGE CARDIFF CONSULTANTS LIMITED (GB) 2001-11-08 WO disclosed
JP-2000204052-A TRIPHENYLENE DIACETYLENE COMPOUND, AND LIQUID CRYSTAL COMPOSITION CONTAINING THE COMPOUND AND LIQUID CRYSTAL DISPLAY IND TECHNOL RES INST 2000-07-25 JP disclosed
EP-0409634-A2 Liquid crystal compounds and optically active compounds SANYO CHEMICAL INDUSTRIES LTD. (JP) 1991-01-23 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 (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-20020019370-A1 Palladium catalyzed arylation, alkylation, deiodination or debromination DDT, TYR, DDC HSD17B10 1280/4885TSHR 175/4885ESR1 4004/4885

“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.