SCHEMBL629963

SCHEMBL629963

Clc1nccc2ccc(Br)cc12

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PLAU P00749 2/20 0.51
PLG P00747 1/20 0.51
PLAT P00750 1/20 0.51
LMNA P02545 2/20 0.47
CYP3A4 P08684 1/20 0.47
MAPT P10636 1/20 0.47
APEX1 P27695 1/20 0.47
MAPK1 P28482 1/20 0.47
PMP22 Q01453 1/20 0.47
PARG Q86W56 1/20 0.42
CYP1A2 P05177 3/20 0.41
HTT P42858 2/20 0.41
CYP2C19 P33261 2/20 0.41
NT5E P21589 1/20 0.39
HIPK2 Q9H2X6 1/20 0.36
CYP2D6 P10635 1/20 0.36
CYP2C9 P11712 1/20 0.36
RXFP1 Q9HBX9 1/20 0.36
PDPK1 O15530 1/20 0.36
CCNB2 O95067 1/20 0.36

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
SCHEMBL29439750 1.00 PLAU (0.51) PLAUPLGPLATLMNACYP3A4
SCHEMBL1536295 0.84 PLAU (0.51) PLAUPLGPLATLMNACYP3A4
SCHEMBL30111349 0.84 PLAU (0.51) PLAUPLGPLATLMNACYP3A4
SCHEMBL1317870 0.79 LMNA (0.50) LMNACYP3A4MAPTAPEX1MAPK1
SCHEMBL29786977 0.79 LMNA (0.50) LMNACYP3A4MAPTAPEX1MAPK1
SCHEMBL25368878 0.76 MAPT (0.47) PLAULMNACYP3A4MAPTAPEX1
SCHEMBL1243375 0.76 CYP3A4 (0.47) LMNACYP3A4MAPTAPEX1MAPK1
SCHEMBL664591 0.76 LMNA (0.47) LMNACYP3A4MAPTAPEX1MAPK1
SCHEMBL30497190 0.76 LMNA (0.47) LMNACYP3A4MAPTAPEX1MAPK1
SCHEMBL13334192 0.76 LMNA (0.47) PLAUPLGPLATLMNACYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260125357-A1 LACTATE ENHANCING COMPOUNDS AND USES THEREOF GLIAPHARM SA (CH) 2026-05-07 US disclosed
US-12617789-B2 Small molecular inhibitors of NF-κb inducing kinase JANSSEN PHARMACEUTICA NV (BE) 2026-05-05 US disclosed
US-20260062443-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS ALEXION PHARMA INC (US) 2026-03-05 US disclosed
US-12534455-B2 Phthalazine derivatives as P2X3 inhibitors CHIESI FARMACEUTICI S.P.A. (IT) 2026-01-27 US disclosed
US-20250188072-A1 COMPOUNDS FOR TREATMENT OF CANCER UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2025-06-12 US disclosed
CN-120035439-A Lactic acid enhancing compounds and uses thereof 格莱制药股份有限公司 2025-05-23 CN disclosed
EP-4548937-A1 ANTIBODY-DRUG COMPLEX Eisai R&D Management Co., Ltd. (JP) 2025-05-07 EP disclosed
EP-4251273-B1 PHTHALAZINE DERIVATIVES AS P2X3 INHIBITORS CHIESI FARM SPA (IT) 2025-03-12 EP disclosed
WO-2025049976-A1 COMPOUNDS AND COMPOSITIONS AS CBP/P300 DEGRADERS AND USES THEREOF ONCOPIA THERAPEUTICS, INC. D/B/A SK LIFE SCIENCE LABS (US) 2025-03-06 WO disclosed
CN-119504706-A Macrocyclic compounds having farnesyl transferase inhibitory activity 库拉肿瘤学公司 2025-02-25 CN disclosed
US-6248738-B1 ANTIULCER AGENTS, ANGIOGENESIS INHIBITORS, ANTIMETASTASIS AGENTS, ANTITUMOR AGENTS PFIZER INC. 2001-06-19 US disclosed
US-6194409-B1 SERINE PROTEASE INHIBITOR; BIOAVAILABILITY WHEN ADMINISTERED BY MOUTH AKZO NOBEL N.V. (NL) 2001-02-27 US disclosed
WO-2001012600-A1 INHIBITORS OF FACTOR Xa COR THERAPEUTICS, INC. (US) 2001-02-22 WO disclosed
CN-1275979-A Isoquinoline compounds useful as urokinase inhibitors PFIZER (US) 2000-12-06 CN disclosed
WO-2000071512-A1 INHIBITORS OF FACTOR Xa COR THERAPEUTICS, INC. (US) 2000-11-30 WO disclosed
WO-2000047554-A2 INHIBITORS OF FACTOR Xa COR THERAPEUTICS INC. (US) 2000-08-17 WO disclosed
EP-1023268-A1 ISOQUINOLINES AS UROKINASE INHIBITORS Pfizer Limited (GB) 2000-08-02 EP disclosed
EP-0975600-A1 HETEROCYCLIC DERIVATIVES AND THEIR USE AS ANTITHROMBOTIC AGENTS Akzo Nobel N.V. (NL) 2000-02-02 EP disclosed
WO-1999020608-A1 ISOQUINOLINES AS UROKINASE INHIBITORS PFIZER LIMITED (GB) 1999-04-29 WO disclosed
WO-1998047876-A1 HETEROCYCLIC DERIVATIVES AND THEIR USE AS ANTITHROMBOTIC AGENTS AKZO NOBEL N.V. (NL) 1998-10-29 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 (5 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-20260062443-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS C9, SSB, C1S PLAU 2528/4885PLG 1785/4885PLAT 2502/4885
US-12534455-B2 Phthalazine derivatives as P2X3 inhibitors P2RX3, P2RX5, P2RX7 PLAU 4124/4885PLG 4628/4885PLAT 4463/4885
US-20260125357-A1 LACTATE ENHANCING COMPOUNDS AND USES THEREOF LDHA, PC, LDHB PLAU 3557/4885PLG 2191/4885PLAT 4103/4885
US-12617789-B2 Small molecular inhibitors of NF-κb inducing kinase IRAK3, IKBKB, IKBKG PLAU 4733/4885PLG 4478/4885PLAT 4831/4885
US-20250188072-A1 COMPOUNDS FOR TREATMENT OF CANCER KLK3, BRDT, ACP3 PLAU 1220/4885PLG 1249/4885PLAT 1610/4885

“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.