Doxycycline Anhydrous

Doxycycline Anhydrous

SCHEMBL29947847

C[C@H]1c2cccc(O)c2C(=O)C2=C(O)[C@]3(O)C(=O)C(C(N)=O)=C(O)[C@@H](N(C)C)[C@@H]3[C@@H](O)[C@@H]21.Cl

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Doxycycline Anhydrous. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MMP7 known ✓ P09237 1/20 0.68
MMP8 known ✓ P22894 1/20 0.68
MMP13 known ✓ P45452 1/20 0.68
TDP1 Q9NUW8 10/20 0.70
KDM4E B2RXH2 9/20 0.70
L3MBTL1 Q9Y468 7/20 0.70
USP2 O75604 6/20 0.70
HSD17B10 Q99714 6/20 0.69
HIF1A Q16665 3/20 0.69
TSHR P16473 1/20 0.69
MMP2 P08253 1/20 0.68
MMP3 P08254 1/20 0.68
ADORA1 P30542 1/20 0.68
ADRA1A P35348 1/20 0.68
RECQL P46063 7/20 0.65
PLA2G1B P04054 1/20 0.65
ATG4B Q9Y4P1 1/20 0.65
HPGD P15428 7/20 0.50
MEN1 O00255 6/20 0.50
KMT2A Q03164 6/20 0.50

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
Doxycycline Anhydrous SCHEMBL40834 1.00 TDP1 (0.70) TDP1KDM4EL3MBTL1USP2HSD17B10
Doxycycline Anhydrous SCHEMBL40836 1.00 TDP1 (0.70) TDP1KDM4EL3MBTL1USP2HSD17B10
Doxycycline Anhydrous SCHEMBL1200549 1.00 TDP1 (0.70) TDP1KDM4EL3MBTL1USP2HSD17B10
Doxycycline Anhydrous SCHEMBL8709954 1.00 TDP1 (0.70) TDP1KDM4EL3MBTL1USP2HSD17B10
Doxycycline Anhydrous SCHEMBL29151798 0.99 TDP1 (0.69) TDP1KDM4EL3MBTL1USP2HSD17B10
Doxycycline Anhydrous SCHEMBL497165 0.99 TDP1 (0.69) TDP1KDM4EL3MBTL1USP2HSD17B10
Doxycycline Anhydrous SCHEMBL497163 0.99 TDP1 (0.69) TDP1KDM4EL3MBTL1USP2HSD17B10
Doxycycline Anhydrous SCHEMBL229272 0.99 TDP1 (0.69) TDP1KDM4EL3MBTL1USP2HSD17B10
Doxycycline Anhydrous SCHEMBL8709949 0.99 TDP1 (0.69) TDP1KDM4EL3MBTL1USP2HSD17B10
Doxycycline Anhydrous SCHEMBL17747966 0.99 TDP1 (0.69) TDP1KDM4EL3MBTL1USP2HSD17B10

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119607009-A Application of radix tetrastigme polysaccharide combined anthracycline compound in preparation of triple negative breast cancer treatment drugs 浙江中医药大学 2025-03-14 CN disclosed
CN-116327708-B Method for preparing nano-particles and method for preparing nano-drug-carrying particles 西南交通大学 2024-11-12 CN disclosed
CN-118415987-A Baicalin liposome and preparation method and application thereof 齐鲁工业大学(山东省科学院) 2024-08-02 CN disclosed
CN-115970658-A Preparation method and application of zero-valent iron-based covalent organic framework composite material 西华师范大学 2023-04-18 CN disclosed
EP-4057814-A1 ANTIMICROBIAL AND ANTIVIRAL, BIOLOGICALLY ACTIVE POLYMER COMPOSITES EFFECTIVE AGAINST SARS-COV-2 AND OTHER VIRAL, BACTERIAL AND FUNGAL TARGETS, AND RELATED METHODS, MATERIALS, COATINGS AND DEVICES Iasis Molecular Sciences, Inc. (US) 2022-09-21 EP disclosed