SCHEMBL763400

SCHEMBL763400

COc1cc2cc(c1Cl)N(C)C(=O)CC(OC(=O)C(C)N(C)C(=O)CCC(C)(C)S)C1(C)OC1C(C)C1CC(O)(NC(=O)O1)C(OC)/C=C/C=C(\C)C2

nearest known ligand 0.83

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TUBB4A P04350 4/20 0.83
TUBB P07437 4/20 0.83
TUBA3C P0DPH7 4/20 0.83
TUBA1B P68363 4/20 0.83
TUBA4A P68366 4/20 0.83
TUBB4B P68371 4/20 0.83
TUBB3 Q13509 4/20 0.83
TUBB2A Q13885 4/20 0.83
TUBB8 Q3ZCM7 4/20 0.83
TUBA3E Q6PEY2 4/20 0.83
TUBA1A Q71U36 4/20 0.83
TUBA1C Q9BQE3 4/20 0.83
TUBB6 Q9BUF5 4/20 0.83
TUBB2B Q9BVA1 4/20 0.83
TUBB1 Q9H4B7 4/20 0.83
CYP2D6 P10635 1/20 0.79
TSHR P16473 1/20 0.79
CYP2C19 P33261 1/20 0.79
HIF1A Q16665 1/20 0.79
P4HB P07237 1/20 0.70

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
SCHEMBL19682095 1.00 TUBB4A (0.83) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL22651647 1.00 TUBB4A (0.83) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL14573126 1.00 TUBB4A (0.83) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL22372700 1.00 TUBB4A (0.83) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL22580752 1.00 TUBB4A (0.83) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL21127723 1.00 TUBB4A (0.83) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL19725996 1.00 TUBB4A (0.83) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL12719514 1.00 TUBB4A (0.83) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL21729001 1.00 TUBB4A (0.83) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL20822457 1.00 TUBB4A (0.83) TUBB4ATUBBTUBA3CTUBA1BTUBA4A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11744900-B2 Preparation of maytansinoid antibody conjugates by a one-step process IMMUNOGEN, INC. (US) 2023-09-05 US disclosed
US-11732038-B2 Conjugates comprising cell-binding agents and cytotoxic agents IMMUNOGEN, INC. (US) 2023-08-22 US disclosed
US-20230181755-A1 ANTITUMOR COMBINATIONS CONTAINING ANTI-CEACAM5 ANTIBODY CONJUGATES, TRIFLURIDINE AND TIPIRACIL SANOFI (FR) 2023-06-15 US disclosed
US-20230181755-A1 ANTITUMOR COMBINATIONS CONTAINING ANTI-CEACAM5 ANTIBODY CONJUGATES, TRIFLURIDINE AND TIPIRACIL SANOFI (FR) 2023-06-15 US disclosed
US-20230158168-A1 PROCESS FOR PREPARING PURIFIED DRUG CONJUGATES IMMUNOGEN, INC. 2023-05-25 US disclosed
US-20230151088-A1 ANTITUMOR COMBINATIONS CONTAINING ANTI-CEACAM5 ANTIBODY CONJUGATES AND FOLFOX SANOFI (FR) 2023-05-18 US disclosed
US-20230149557-A1 ANTITUMOR COMBINATIONS CONTAINING ANTI-CEACAM5 ANTIBODY CONJUGATES AND CETUXIMAB SANOFI (FR) 2023-05-18 US disclosed
US-11471536-B2 Process for preparing purified drug conjugates IMMUNOGEN, INC. (US) 2022-10-18 US disclosed
US-20220202946-A1 CEACAM5 ANTIBODY-DRUG CONJUGATE FORMULATION SANOFI (FR) 2022-06-30 US disclosed
US-11332542-B2 Anti-CEACAM5 antibodies and uses thereof SANOFI (FR) 2022-05-17 US disclosed
US-20070270585-A1 Maytansinoid intermediates: N-alkyl- or aryldithioalkanoylalanines and N-alkanoyl- or aroylthioalkanoylalanines, e.g., N-methyl-N-(4-methyl-4-methyldithio-1-oxopentyl)-alanine; optical isomers and racemic mixtures; preparations from isobutylene sulfide and acetonitrile, methyl methanethiosulfonate, etc. IMMUNOGEN, INC. (US) 2007-11-22 US disclosed
US-20070264266-A1 Maytansine derivatives having a sterically hindered thiol or disulfide groups, capable of conjugating to cell-binding agents, to form drugs having improved therapeutic efficacy in animal tumor models; antitumor agents IMMUNOGEN INC. (US) 2007-11-15 US disclosed
US-20070264266-A1 Maytansine derivatives having a sterically hindered thiol or disulfide groups, capable of conjugating to cell-binding agents, to form drugs having improved therapeutic efficacy in animal tumor models; antitumor agents IMMUNOGEN INC. (US) 2007-11-15 US disclosed
US-7276497-B2 For therapy of tumors IMMUNOGEN INC. 2007-10-02 US disclosed
US-7276497-B2 For therapy of tumors IMMUNOGEN INC. 2007-10-02 US disclosed
WO-2007024536-A2 PROCESS FOR PREPARING MAYTANSINOID ANTIBODY CONJUGATES IMMUNOGEN, INC. (US) 2007-03-01 WO disclosed
US-20070048314-A1 preparing a cell-binding agent chemically coupled to a drug; covalently attaching a linker to a cell-binding agent, a purification step, conjugating a drug to the cell-binding agent and a subsequent purification step; high purity and stability IMMUNOGEN, INC. (US) 2007-03-01 US disclosed
US-20070048314-A1 preparing a cell-binding agent chemically coupled to a drug; covalently attaching a linker to a cell-binding agent, a purification step, conjugating a drug to the cell-binding agent and a subsequent purification step; high purity and stability IMMUNOGEN, INC. (US) 2007-03-01 US disclosed
WO-2007019232-A2 IMMUNOCONJUGATE FORMULATIONS IMMUNOGEN, INC. (US) 2007-02-15 WO disclosed
US-20070031402-A1 Immunoconjugate formulations IMMUNOGEN INC. 2007-02-08 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 (13 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-20220202946-A1 CEACAM5 ANTIBODY-DRUG CONJUGATE FORMULATION CD44, EPCAM, CD22 TUBB4A 565/4885TUBB 1029/4885TUBA3C 1467/4885
US-20070048314-A1 preparing a cell-binding agent chemically coupled to a drug; covalently attaching a linker to a cell-binding agent, a purification step, conjugating a drug to the cell-binding agent and a subsequent purification step; high purity and stability EPCAM, VCAM1, CD44 TUBB4A 104/4885TUBB 163/4885TUBA3C 469/4885
US-20070264266-A1 Maytansine derivatives having a sterically hindered thiol or disulfide groups, capable of conjugating to cell-binding agents, to form drugs having improved therapeutic efficacy in animal tumor models; antitumor agents SPR, SDAD1, ARRB1 TUBB4A 548/4885TUBB 703/4885TUBA3C 1070/4885
US-20070270585-A1 Maytansinoid intermediates: N-alkyl- or aryldithioalkanoylalanines and N-alkanoyl- or aroylthioalkanoylalanines, e.g., N-methyl-N-(4-methyl-4-methyldithio-1-oxopentyl)-alanine; optical isomers and racemic mixtures; preparations from isobutylene sulfide and acetonitrile, methyl methanethiosulfonate, etc. AASDHPPT, AADAT, SLC6A15 TUBB4A 2306/4885TUBB 2899/4885TUBA3C 3933/4885
US-20230158168-A1 PROCESS FOR PREPARING PURIFIED DRUG CONJUGATES EPCAM, CD44, NAPA TUBB4A 139/4885TUBB 254/4885TUBA3C 357/4885
US-11332542-B2 Anti-CEACAM5 antibodies and uses thereof EPCAM, SIGLEC9, TMEM205 TUBB4A 650/4885TUBB 662/4885TUBA3C 200/4885
US-11732038-B2 Conjugates comprising cell-binding agents and cytotoxic agents PCNA, EPCAM, MKI67 TUBB4A 323/4885TUBB 358/4885TUBA3C 793/4885
US-20230181755-A1 ANTITUMOR COMBINATIONS CONTAINING ANTI-CEACAM5 ANTIBODY CONJUGATES, TRIFLURIDINE AND TIPIRACIL TAS2R5, TMEM205, CD99 TUBB4A 853/4885TUBB 690/4885TUBA3C 348/4885
US-20230151088-A1 ANTITUMOR COMBINATIONS CONTAINING ANTI-CEACAM5 ANTIBODY CONJUGATES AND FOLFOX FOLR1, FOLR2, ITGA5 TUBB4A 1258/4885TUBB 1089/4885TUBA3C 742/4885
US-20230149557-A1 ANTITUMOR COMBINATIONS CONTAINING ANTI-CEACAM5 ANTIBODY CONJUGATES AND CETUXIMAB EPCAM, CA13, CA14 TUBB4A 1543/4885TUBB 2006/4885TUBA3C 714/4885
US-20070031402-A1 Immunoconjugate formulations CD44, SLC6A5, SI TUBB4A 2623/4885TUBB 1517/4885TUBA3C 1768/4885
US-11744900-B2 Preparation of maytansinoid antibody conjugates by a one-step process CD47, CD22, CLSPN TUBB4A 1345/4885TUBB 2767/4885TUBA3C 2822/4885
US-11471536-B2 Process for preparing purified drug conjugates EPCAM, CD44, NAPA TUBB4A 139/4885TUBB 254/4885TUBA3C 357/4885

“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.