SCHEMBL238785

SCHEMBL238785

Nc1cc(-c2ccncc2)n[nH]1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MKNK2 Q9HBH9 2/20 0.47
MKNK1 Q9BUB5 1/20 0.47
PDPK1 O15530 2/20 0.44
JAK2 O60674 1/20 0.44
IDO1 P14902 1/20 0.44
PDE3B Q13370 3/20 0.42
PDE3A Q14432 3/20 0.42
LMNA P02545 2/20 0.42
MAPT P10636 2/20 0.42
ALDH1A1 P00352 2/20 0.42
CYP1A2 P05177 2/20 0.42
CYP3A4 P08684 2/20 0.42
AURKB Q96GD4 2/20 0.42
INCENP Q9NQS7 2/20 0.42
KDM4E B2RXH2 1/20 0.42
MEN1 O00255 1/20 0.42
AURKA O14965 1/20 0.42
GLA P06280 1/20 0.42
CYP2D6 P10635 1/20 0.42
THRB P10828 1/20 0.42

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
SCHEMBL11242864 0.81 PDE3B (0.61) MKNK2MKNK1PDPK1JAK2IDO1
SCHEMBL168659 0.81 POLB (0.61) MKNK2MKNK1LMNACYP1A2AURKB
SCHEMBL28466328 0.81 ALPL (0.58) PDE3BPDE3ALMNAMAPTALDH1A1
Hydrochloric Acid SCHEMBL9124767 0.79 ALPL (0.56) PDE3BPDE3ALMNAMAPTALDH1A1
Hydrochloric Acid SCHEMBL11246455 0.78 PDE3B (0.58) MKNK2MKNK1PDPK1JAK2PDE3B
SCHEMBL1143959 0.78 ALPL (0.54) LMNAMAPTCYP1A2CYP3A4MEN1
SCHEMBL1143098 0.78 SMN1; SMN2 (0.61) JAK2LMNAMAPTALDH1A1CYP1A2
SCHEMBL244618 0.78 ALPL (0.54) MKNK2MKNK1MAPTALDH1A1KDM4E
SCHEMBL18966078 0.78 METAP2 (0.46) PDE3BPDE3AMAPTSMN1; SMN2PDE2A
SCHEMBL474802 0.78 ALPL (0.54) MKNK2MKNK1LMNAMAPTMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12404265-B2 Substituted pyridine derivatives as SARM1 inhibitors NURA BIO, INC. (US) 2025-09-02 US disclosed
CN-115209952-B Substituted pyrazolopyrimidines and use thereof 维基分析有限公司 2025-05-30 CN disclosed
US-12275739-B2 Inhibitors of menin-MLL interaction BIOMEA FUSION, INC. (US) 2025-04-15 US disclosed
US-20240140953-A1 INHIBITORS OF MENIN-MLL INTERACTION BIOMEA FUSION, INC. 2024-05-02 US disclosed
US-11970481-B1 Substituted pyridine derivatives as SARM1 inhibitors NURA BIO, INC. (US) 2024-04-30 US disclosed
US-20240116901-A1 SUBSTITUTED PYRIDINE DERIVATIVES AS SARM1 INHIBITORS NURA BIO, INC. 2024-04-11 US disclosed
US-20240018151-A1 NOVEL INHIBITORS OF PIKFYVE AND METHODS USING SAME TME THERAPEUTICS LLC 2024-01-18 US disclosed
US-20240018151-A1 NOVEL INHIBITORS OF PIKFYVE AND METHODS USING SAME TME THERAPEUTICS LLC 2024-01-18 US disclosed
US-11845753-B2 Inhibitors of menin-mll interaction BIOMEA FUSION, INC. (US) 2023-12-19 US disclosed
US-20230339913-A1 SUBSTITUTED PYRIDINE DERIVATIVES AS SARM1 INHIBITORS NURA BIO, INC. 2023-10-26 US disclosed
US-20050272709-A1 Immugenic compositions and diagnostic and therapeutic uses thereof DERMIRA (CANADA), INC. 2005-12-08 US disclosed
WO-2005105780-A2 COMPOSITIONS USEFUL AS INHIBITORS OF ROCK AND OTHER PROTEIN KINASES VERTEX PHARMACEUTICALS INCORPORATED (US) 2005-11-10 WO disclosed
US-20050113283-A1 Methods of treating conditions associated with an EDG-4 receptor MANIV ENERGY CAPITAL 2005-05-26 US disclosed
EP-1513522-A2 METHODS OF TREATING CONDITIONS ASSOCIATED WITH AN EDG RECEPTOR SRI INTERNATIONAL (US) 2005-03-16 EP disclosed
EP-1450791-A1 HYDRAZONOPYRAZOLE DERIVATIVES AND THEIR USE AS THERAPEUTICS Kinetek Pharmaceuticals, Inc. (CA) 2004-09-01 EP disclosed
US-6649759-B2 Pyrazolo(1,5-a)pyrimidine derivatives; treating feeding, cardiovascular and psychological disorders PFIZER INC. 2003-11-18 US disclosed
WO-2003062392-A2 METHODS OF TREATING CONDITIONS ASSOCIATED WITH AN EDG RECEPTOR CERETEK LLC (US) 2003-07-31 WO disclosed
WO-2003045379-A1 HYDRAZONOPYRAZOLE DERIVATIVES AND THEIR USE AS THERAPEUTICS KINETEK PHARMACEUTICALS, INC. (CA) 2003-06-05 WO disclosed
US-20030100546-A1 Neuropeptide Y antagonists ELLIOTT RICHARD L (US) 2003-05-29 US disclosed
US-20020061897-A1 Neuropeptide Y antagonists ELLIOTT RICHARD L (US) 2002-05-23 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 (12 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-12404265-B2 Substituted pyridine derivatives as SARM1 inhibitors SARM1, SARNP, ADRM1 MKNK2 389/4885MKNK1 395/4885PDPK1 545/4885
US-12275739-B2 Inhibitors of menin-MLL interaction MLLT1, MEN1, MLLT3 MKNK2 22/4885MKNK1 26/4885PDPK1 1267/4885
US-20030100546-A1 Neuropeptide Y antagonists NPY1R, NPY2R, GIPR MKNK2 2098/4885MKNK1 1839/4885PDPK1 1844/4885
US-20050272709-A1 Immugenic compositions and diagnostic and therapeutic uses thereof MKI67, CDK4, CCNC MKNK2 513/4885MKNK1 387/4885PDPK1 121/4885
US-11970481-B1 Substituted pyridine derivatives as SARM1 inhibitors SARM1, SARNP, ADRM1 MKNK2 389/4885MKNK1 395/4885PDPK1 545/4885
US-20230339913-A1 SUBSTITUTED PYRIDINE DERIVATIVES AS SARM1 INHIBITORS SARM1, SARNP, ADRM1 MKNK2 389/4885MKNK1 395/4885PDPK1 545/4885
US-20020061897-A1 Neuropeptide Y antagonists NPY1R, NPY2R, GIPR MKNK2 2098/4885MKNK1 1839/4885PDPK1 1844/4885
US-20240018151-A1 NOVEL INHIBITORS OF PIKFYVE AND METHODS USING SAME PIKFYVE, PIK3CD, PIK3R5 MKNK2 101/4885MKNK1 83/4885PDPK1 10/4885
US-20240116901-A1 SUBSTITUTED PYRIDINE DERIVATIVES AS SARM1 INHIBITORS SARM1, SARNP, ADRM1 MKNK2 389/4885MKNK1 395/4885PDPK1 545/4885
US-20240140953-A1 INHIBITORS OF MENIN-MLL INTERACTION MLLT1, MEN1, MLLT3 MKNK2 22/4885MKNK1 26/4885PDPK1 1267/4885
US-20050113283-A1 Methods of treating conditions associated with an EDG-4 receptor EDNRA, EDNRB, ESRRG MKNK2 4321/4885MKNK1 4518/4885PDPK1 4310/4885
US-11845753-B2 Inhibitors of menin-mll interaction MLLT1, MEN1, MLLT3 MKNK2 22/4885MKNK1 26/4885PDPK1 1267/4885

“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.