SCHEMBL10604135

SCHEMBL10604135

N=C(N)NCCc1ccc(C(=O)O)cc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ST14 Q9Y5Y6 2/20 0.61
CA2 P00918 3/20 0.49
CA9 Q16790 2/20 0.49
LMNA P02545 1/20 0.49
HTT P42858 1/20 0.49
CA12 O43570 2/20 0.47
CA1 P00915 2/20 0.47
F2 P00734 1/20 0.47
ITGB3 P05106 1/20 0.47
ITGA2B P08514 1/20 0.47
KMT2A Q03164 1/20 0.46
HDAC2 Q92769 1/20 0.45
HDAC8 Q9BY41 1/20 0.45
HDAC6 Q9UBN7 1/20 0.45
ALDH1A1 P00352 1/20 0.44
NPC1 O15118 3/20 0.44
RAB9A P51151 3/20 0.44
RARB P10826 1/20 0.44
USP28 Q96RU2 1/20 0.43
USP25 Q9UHP3 1/20 0.43

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
Hydrochloric Acid SCHEMBL7327788 0.98 ST14 (0.59) ST14CA2CA9LMNAHTT
SCHEMBL30503474 0.88 ST14 (0.63) ST14CA2CA9CA12CA1
SCHEMBL28416786 0.86 ST14 (0.56) ST14CA2CA9LMNAHTT
SCHEMBL4104833 0.82 KMT2A (0.62) ST14F2KMT2AALDH1A1
SCHEMBL24892365 0.81 ST14 (0.55) ST14CA2CA9LMNACA12
SCHEMBL20486525 0.81 FOLH1 (0.50) CA2CA1HDAC2HDAC8HDAC6
Hydrochloric Acid SCHEMBL3883713 0.81 KMT2A (0.61) ST14F2KMT2AALDH1A1
SCHEMBL17198821 0.80 NPC1 (0.55) ST14CA2CA9LMNACA12
Hydrochloric Acid SCHEMBL7324472 0.80 USP28 (0.49) CA2CA1HDAC2HDAC8HDAC6
SCHEMBL12401907 0.80 ST14 (0.51) ST14CA2LMNACA1ITGB3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4191779-A P-SUBSTITUTED BENZOIC ACID STANLEY DRUG PRODUCTS, INC. (US) 1980-03-04 US claimed
US-12569566-B2 Compositions containing, methods and uses of antibody-TLR agonist conjugates AMBRX, INC. (US) 2026-03-10 US disclosed
CN-119455003-A Compositions, methods and uses comprising antibody-TLR agonist conjugates AMBRX公司 2025-02-18 CN disclosed
CN-119455004-A Compositions, methods and uses comprising antibody-TLR agonist conjugates AMBRX公司 2025-02-18 CN disclosed
CN-113660957-B Compositions, methods and uses comprising antibody-TLR agonist conjugates AMBRX公司 2024-12-13 CN disclosed
US-20230302150-A1 ANTIBODY-TLR AGONIST CONJUGATES, METHODS AND USES THEREOF AMBRX, INC. (US) 2023-09-28 US disclosed
US-20230302150-A1 ANTIBODY-TLR AGONIST CONJUGATES, METHODS AND USES THEREOF AMBRX, INC. (US) 2023-09-28 US disclosed
US-20230302150-A1 ANTIBODY-TLR AGONIST CONJUGATES, METHODS AND USES THEREOF AMBRX, INC. (US) 2023-09-28 US disclosed
CN-116457023-A antibody-TLR agonist conjugates, methods and uses thereof AMBRX公司 2023-07-18 CN disclosed
EP-4199968-A1 ANTIBODY-TLR AGONIST CONJUGATES, METHODS AND USES THEREOF Ambrx, Inc. (US) 2023-06-28 EP disclosed
CN-113660957-A Compositions, methods, and uses comprising antibody-TLR agonist conjugates AMBRX公司 2021-11-16 CN disclosed
EP-3589631-B1 IMIDAZO[4,5-C]RING COMPOUNDS CONTAINING GUANIDINE SUBSTITUTED BENZAMIDE GROUPS 3M INNOVATIVE PROPERTIES CO (US) 2021-07-21 EP disclosed
US-10766896-B2 Imidazo[4,5-c] ring compounds containing guanidine substituted benzamide groups 3M INNOVATIVE PROPERTIES COMPANY (US) 2020-09-08 US disclosed
WO-2020168017-A1 COMPOSITIONS CONTAINING, METHODS AND USES OF ANTIBODY-TLR AGONIST CONJUGATES AMBRX, INC. (US) 2020-08-20 WO disclosed
WO-2020168017-A1 COMPOSITIONS CONTAINING, METHODS AND USES OF ANTIBODY-TLR AGONIST CONJUGATES AMBRX, INC. (US) 2020-08-20 WO disclosed
US-20200087298-A1 Imidazo[4,5-c] Ring Compounds Containing Guanidine Substituted Benzamide Groups SOLVENTUM INTELLECTUAL PROPERTIES COMPANY 2020-03-19 US disclosed
WO-2018160552-A1 IMIDAZO[4,5-c] RING COMPOUNDS CONTAINING GUANIDINE SUBSTITUTED BENZAMIDE GROUPS 3M INNOVATIVE PROPERTIES COMPANY (US) 2018-09-07 WO disclosed
EP-0218027-B1 NOVEL GUANIDINOMETHYLBENZOIC ACID DERIVATIVES Kabushiki Kaisha Med-Creat (JP) 1989-09-20 EP disclosed
EP-0218027-A1 Novel guanidinomethylbenzoic acid derivatives Kabushiki Kaisha Med-Creat (JP) 1987-04-15 EP disclosed
US-4191779-A P-SUBSTITUTED BENZOIC ACID STANLEY DRUG PRODUCTS, INC. (US) 1980-03-04 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 (4 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-20200087298-A1 Imidazo[4,5-c] Ring Compounds Containing Guanidine Substituted Benzamide Groups IL4, IFNG, IFNAR1 ST14 2613/4885CA2 3140/4885CA9 4125/4885
US-20230302150-A1 ANTIBODY-TLR AGONIST CONJUGATES, METHODS AND USES THEREOF TLR3, TLR1, TLR9 ST14 1010/4885CA2 4583/4885CA9 3807/4885
US-10766896-B2 Imidazo[4,5-c] ring compounds containing guanidine substituted benzamide groups IL4, IFNG, IFNAR1 ST14 2613/4885CA2 3140/4885CA9 4125/4885
US-12569566-B2 Compositions containing, methods and uses of antibody-TLR agonist conjugates TLR3, TLR2, TLR1 ST14 1783/4885CA2 2367/4885CA9 2006/4885

“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.