SCHEMBL13826136

SCHEMBL13826136

N#Cc1c(N(c2ccccc2)c2ccccc2)c(F)c(N(c2ccccc2)c2ccccc2)c(F)c1N(c1ccccc1)c1ccccc1

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.38
TSHR P16473 2/20 0.38
LMNA P02545 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
CTSK P43235 1/20 0.36
ALDH1A1 P00352 6/20 0.35
KDM4E B2RXH2 3/20 0.35
TDP1 Q9NUW8 2/20 0.34
CYP1A2 P05177 1/20 0.34
CYP3A4 P08684 1/20 0.34
CYP2D6 P10635 1/20 0.34
CYP2C9 P11712 1/20 0.34
CYP2C19 P33261 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
CRHBP P24387 1/20 0.34
CRHR2 Q13324 1/20 0.34
NPSR1 Q6W5P4 1/20 0.34
ADORA1 P30542 5/20 0.33
ADORA2A P29274 4/20 0.33
MEN1 O00255 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
SCHEMBL27245264 0.96 MAPT (0.38) MAPTTSHRLMNASMN1; SMN2CTSK
SCHEMBL22124615 0.89 ADORA1 (0.40) KDM4ENPSR1ADORA1ADORA2AMEN1
SCHEMBL13826028 0.85 MAPT (0.43) MAPTTSHRLMNASMN1; SMN2CTSK
SCHEMBL13826009 0.85 ALDH1A1 (0.44) MAPTTSHRALDH1A1KDM4ETDP1
SCHEMBL29176116 0.81 MAPT (0.41) MAPTTSHRLMNASMN1; SMN2CTSK
SCHEMBL16215950 0.78 ALDH1A1 (0.42) MAPTTSHRALDH1A1KDM4ETDP1
SCHEMBL16122511 0.77 ADORA1 (0.36) MAPTTSHRLMNASMN1; SMN2ALDH1A1
SCHEMBL31145578 0.76 MAPT (0.38) MAPTTSHRLMNASMN1; SMN2CTSK
SCHEMBL20657775 0.76 ALDH1A1 (0.48) MAPTTSHRLMNASMN1; SMN2CTSK
SCHEMBL2453584 0.76 MAPT (0.34) MAPTTSHRLMNASMN1; SMN2CTSK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122011026-A Asymmetric bidentate phosphine ligand and synthesis method thereof 淮北师范大学 2026-05-12 CN claimed
CN-122010810-A The method comprises the following steps of18F-marked difluoromethyl seleno ether compound, and synthetic method and application thereof 江苏省原子医学研究所 2026-05-12 CN claimed
CN-118994157-A 3-Spiro indoline derivative containing trifluoromethyl and preparation method thereof 西北师范大学 2024-11-22 CN claimed
CN-118812428-A 3-Trifluoromethyl tetrahydroquinoline compound and preparation method thereof 西北师范大学 2024-10-22 CN claimed
CN-117924125-A Method for preparing sulfonamide derivative through visible light catalysis without metal participation 苏州大学 2024-04-26 CN claimed
CN-117800891-A Preparation method of 3- (2-aminophenyl) pyrrole derivative 深圳职业技术学院 2024-04-02 CN claimed
CN-117430542-B Synthesis method of trifluoromethyl indole derivative 上海恩氟佳科技有限公司 2024-03-08 CN claimed
CN-117430542-A Synthesis method of trifluoromethyl indole derivative 上海恩氟佳科技有限公司 2024-01-23 CN claimed
CN-117384178-A Preparation method of 2, 3-dihydrobenzopyran-4-ketorolane derivatives 深圳职业技术大学 2024-01-12 CN claimed
CN-117164533-A Method for synthesizing furylacetic acid compound by using carbon dioxide 中国科学院兰州化学物理研究所 2023-12-05 CN claimed
CN-117142943-A Method for synthesizing 6-hydroxycaproic acid (ester) by using carbon dioxide and furfuryl alcohol compounds 中国科学院兰州化学物理研究所 2023-12-01 CN claimed
CN-122011026-A Asymmetric bidentate phosphine ligand and synthesis method thereof 淮北师范大学 2026-05-12 CN disclosed
CN-122010810-A The method comprises the following steps of18F-marked difluoromethyl seleno ether compound, and synthetic method and application thereof 江苏省原子医学研究所 2026-05-12 CN disclosed
US-20260055128-A1 ORGANONICKEL INTERMEDIATES USEFUL FOR CARBOXYLATION OF SUBSTRATES WITH CARBON DIOXIDE U.S. DEPARTMENT OF ENERGY 2026-02-26 US disclosed
US-12365678-B2 Pharmaceutical process for the preparation of 4-{4-[(3R)-3-methylmorpholin-4-yl]-6-[1-((R)-S-methylsulfonimidoyl) cyclopropyl]pyrimidin-2-yl}-1H-pyrrolo[2,3-b] pyridine and intermediates ASTRAZENECA AB (SE) 2025-07-22 US disclosed
US-20170179399-A1 COMPOUNDS FOR ELECTRONIC DEVICES MERCK PATENT GMBH (DE) 2017-06-22 US disclosed
EP-2699641-B1 COMPOUNDS FOR ELECTRONIC DEVICES MERCK PATENT GMBH (DE) 2017-05-17 EP disclosed
US-20140231715-A1 COMPOUNDS FOR ELECTRONIC DEVICES MERCK PATENT GMBH PATENTS & SCIENTIFIC INFORMATION (DE) 2014-08-21 US disclosed
US-20140231715-A1 COMPOUNDS FOR ELECTRONIC DEVICES MERCK PATENT GMBH PATENTS & SCIENTIFIC INFORMATION (DE) 2014-08-21 US disclosed
WO-2012143079-A1 COMPOUNDS FOR ELECTRONIC DEVICES MERCK PATENT GMBH (DE) 2012-10-26 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-12365678-B2 Pharmaceutical process for the preparation of 4-{4-[(3R)-3-methylmorpholin-4-yl]-6-[1-((R)-S-methylsulfonimidoyl) cyclopropyl]pyrimidin-2-yl}-1H-pyrrolo[2,3-b] pyridine and intermediates TPMT, CYP3A7, HTR7 MAPT 2037/4885TSHR 1434/4885LMNA 4609/4885
US-20170179399-A1 COMPOUNDS FOR ELECTRONIC DEVICES CYP2C19, CYP1B1, CYP2C9 MAPT 2868/4885TSHR 3743/4885LMNA 3443/4885
US-20260055128-A1 ORGANONICKEL INTERMEDIATES USEFUL FOR CARBOXYLATION OF SUBSTRATES WITH CARBON DIOXIDE MT-CO2, SCO2, ACACA MAPT 3729/4885TSHR 4322/4885LMNA 4716/4885

“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.