SCHEMBL690215

SCHEMBL690215

CN1C[C@@H](O)C[C@@H]1C(=O)O

nearest known ligand 0.59

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
ATM Q13315 1/20 0.59
PIK3CD O00329 2/20 0.33
GAA P10253 1/20 0.33
ALDH1A1 P00352 1/20 0.33
ACE P12821 2/20 0.33
MME P08473 1/20 0.32
TDP1 Q9NUW8 1/20 0.32

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
SCHEMBL689733 1.00 ATM (0.59) ATMPIK3CDGAAALDH1A1ACE
SCHEMBL3674503 1.00 ATM (0.59) ATMPIK3CDGAAALDH1A1ACE
SCHEMBL19080644 1.00 ATM (0.59) ATMPIK3CDGAAALDH1A1ACE
SCHEMBL689912 1.00 ATM (0.59) ATMPIK3CDGAAALDH1A1ACE
SCHEMBL1303907 1.00 ATM (0.59) ATMPIK3CDGAAALDH1A1ACE
SCHEMBL7882438 1.00 ATM (0.59) ATMPIK3CDGAAALDH1A1ACE
SCHEMBL8989612 1.00 ATM (0.59) ATMPIK3CDGAAALDH1A1ACE
SCHEMBL589712 1.00 ATM (0.59) ATMPIK3CDGAAALDH1A1ACE
Hydrochloric Acid SCHEMBL350474 0.98 ATM (0.57) ATMPIK3CDGAAALDH1A1ACE
Hydrochloric Acid SCHEMBL2147938 0.98 ATM (0.57) ATMPIK3CDGAAALDH1A1ACE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240101553-A1 KRAS G12C INHIBITORS MIRATI THERAPEUTICS INC (US) 2024-03-28 US disclosed
US-20230373999-A1 KRAS G12C INHIBITORS MIRATI THERAPEUTICS INC (US) 2023-11-23 US disclosed
EP-3710439-B1 KRAS G12C INHIBITORS MIRATI THERAPEUTICS INC (US) 2023-02-15 EP disclosed
WO-2023272720-A1 HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS OF PD-L1 INTERACTIONS Ascletis BioScience Co., Ltd (CN) 2023-01-05 WO disclosed
US-20220340893-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2022-10-27 US disclosed
US-11254658-B2 Bisamide sarcomere activating compounds and uses thereof AMGEN INC. (US) 2022-02-22 US disclosed
CN-111989321-A KRAS G12C inhibitors 米拉蒂治疗股份有限公司 2020-11-24 CN disclosed
US-20200262837-A1 KRAS G12C INHIBITORS ARRAY BIOPHARMA INC. 2020-08-20 US disclosed
US-10723720-B2 Bisamide sarcomere activating compounds and uses therof AMGEN INC. (US) 2020-07-28 US disclosed
US-20200223829-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF AMGEN INC. 2020-07-16 US disclosed
WO-2010026096-A1 7-(PIPERAZINE-1-YMETHYL)-1H-INDOLE-2-CARBOXYLIC ACID (PHENYL)-AMIDE DERIVATIVES AND ALLIED COMPOUNDS AS P38 MAP KINASE INHIBITORS FOR THE TREATMENT OF RESPIRATORY DISEASES BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2010-03-11 WO disclosed
WO-2010026096-A1 7-(PIPERAZINE-1-YMETHYL)-1H-INDOLE-2-CARBOXYLIC ACID (PHENYL)-AMIDE DERIVATIVES AND ALLIED COMPOUNDS AS P38 MAP KINASE INHIBITORS FOR THE TREATMENT OF RESPIRATORY DISEASES BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2010-03-11 WO disclosed
US-20080234263-A1 Quinazoline Derivatives ASTRAZENECA (SE) 2008-09-25 US disclosed
CN-1275051-A Method for improving the freezing tolerance of plant UNIV DU QUEBEC A MONTREAL (CA) 2000-11-29 CN disclosed
US-5523413-A Process for optically active 2-alkyl-2,5-diazabicyclo[2.2.1] heptanes PFIZER INC. (US) 1996-06-04 US disclosed
US-5475117-A Process for optically active 2-alkyl-2,5-diazabicyclo[2.2.1]heptanes PFIZER, INC. (US) 1995-12-12 US disclosed
US-5371235-A Process for optically active 2-alkyl-2,5-diazabicyclo[2.2.1]heptanes PFIZER INC. (US) 1994-12-06 US disclosed
US-5157125-A Optically active 2-alkyl-2,5-diazabicyclo[2.2.1]heptanes PFIZER INC. (US) 1992-10-20 US disclosed
US-5095121-A Process for optically active 2-alkyl-2,5-diazabicyclo(2.2.1)heptanes PFIZER INC (US) 1992-03-10 US disclosed
US-5013839-A Process for optically active 2-alkyl-2,5-diazabicyclo(2.2.1) heptanes PFIZER INC. (US) 1991-05-07 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 (7 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-20080234263-A1 Quinazoline Derivatives EGFR, ERBB2, ERBB3 ATM 560/4885PIK3CD 272/4885GAA 2323/4885
US-11254658-B2 Bisamide sarcomere activating compounds and uses thereof TNNI3, TNNT2, TNNC1 ATM 3953/4885PIK3CD 1410/4885GAA 2874/4885
US-20200262837-A1 KRAS G12C INHIBITORS KRAS, NRAS, HRAS ATM 3528/4885PIK3CD 253/4885GAA 1367/4885
US-20200223829-A1 BISAMIDE SARCOMERE ACTIVATING COMPOUNDS AND USES THEREOF TNNI3, TNNT2, TNNC1 ATM 3953/4885PIK3CD 1410/4885GAA 2874/4885
US-20240101553-A1 KRAS G12C INHIBITORS KRAS, NRAS, HRAS ATM 3528/4885PIK3CD 253/4885GAA 1367/4885
US-10723720-B2 Bisamide sarcomere activating compounds and uses therof TNNI3, TNNT2, TNNC1 ATM 3596/4885PIK3CD 2436/4885GAA 2907/4885
US-20230373999-A1 KRAS G12C INHIBITORS KRAS, NRAS, HRAS ATM 3528/4885PIK3CD 253/4885GAA 1367/4885

“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.