Clindamycin hydrochloride
Highest phase reached
Approved
Drug type
Small molecule
First approval year
1970
- First approval year
- 1970
- Listing at source
- Listed
- Highest phase reached
- Approved
- Drug type
- Small molecule
- Drug name
- Clindamycin hydrochloride
- Molecular weight
- 461.45
- Structure (SMILES)
- CCC[C@@H]1C[C@@H](C(=O)N[C@@H]([C@H]2O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O)[C@H](C)Cl)N(C)C1.Cl
- cleocin
- Cleocin
- cleocin hydrochloride
- Cleocin hydrochloride
- clindamycin hydrochloride
- Clindamycin hydrochloride
- dalacin c
- Dalacin c
- antirobe
- Antirobe
- Clindamycin (as hydrochloride)
- clindamycin as hydrochloride
- clindamycin hcl
- Clindamycin hcl
- clindamycin hydrochloride
- Clindamycin hydrochloride
- CLINDAMYCIN HYDROCHLORIDE [EP MONOGRAPH]
- CLINDAMYCIN HYDROCHLORIDE [GREEN BOOK]
- CLINDAMYCIN HYDROCHLORIDE [JAN]
- CLINDAMYCIN HYDROCHLORIDE [MART.]
- CLINDAMYCIN HYDROCHLORIDE [MI]
- CLINDAMYCIN HYDROCHLORIDE [ORANGE BOOK]
- CLINDAMYCIN HYDROCHLORIDE [USP MONOGRAPH]
- CLINDAMYCIN HYDROCHLORIDE [USP-RS]
- CLINDAMYCIN HYDROCHLORIDE [VANDF]
- Clindamycin hydrochloride [WHO-DD]
- clindamycin hydrochloride anhydrous
- CLINDAMYCIN HYDROCHLORIDE ANHYDROUS
- clindamycin hydrochloride ep monograph
- clindamycin hydrochloride green book
- clindamycin hydrochloride jan
- clindamycin hydrochloride mart
- clindamycin hydrochloride mi
And 19 more, listed on the interactive page.
- CAS registry numbers
- 21462-39-5
- ChEMBL ID
- CHEMBL1200588
- InChIKey
- AUODDLQVRAJAJM-XJQDNNTCSA-N
- FDA ingredient codes (UNII)
- T20OQ1YN1W
- 16051951
- 118705388
- 21235
- 81982
- Applicant
- PFIZER
- Approval date
- 22 Feb 1970
- Application number
- NDA050162
- Patents
- 0
- Designations
- 1
- First in class
- No
- Fast track
- No
- Breakthrough designation
- No
- Orphan designation
- No
- Priority review
- No
- Orphan exclusivity
- No
- Accelerated approval
- No
- Availability
- Prescription only
- Boxed warning
- Yes
- Drug name stem
- -mycin
Administration routes
- Oral
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P02358
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P02359
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P02413
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7J3
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7J7
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7K2
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7K6
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7L0
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7L3
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7L8
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7M2
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7M6
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7M9
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7N1
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7N4
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7N9
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7P5
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7Q1
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7Q6
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7R5
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7R9
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7S3
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7S9
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Protein identifier
- P0A7T3
And 31 more, listed on the interactive page.
Open Targets mechanisms
- Mechanism
- Bacterial 70S ribosome inhibitor
- Action type
- Inhibitor
- Target
- Bacterial 70S ribosome
- Condition
- Infections
- Highest recorded phase
- 4
- Condition identifier
- EFO:0000544
- Subject identifier
- D007239
- Condition
- Osteomyelitis
- Highest recorded phase
- 0.5
- Condition identifier
- EFO:0003102
- Subject identifier
- D010019
- Condition
- Pneumonia
- Highest recorded phase
- 4
- Condition identifier
- EFO:0003106
- Subject identifier
- D011014
- Condition
- Acne Vulgaris
- Highest recorded phase
- 1
- Condition identifier
- EFO:0003894
- Subject identifier
- D000152
- Condition identifier
- EFO_0000544
- Condition identifier
- EFO_0000544
- Highest recorded phase
- 4
- Condition identifier
- EFO_0003102
- Condition identifier
- EFO_0003106
- Condition identifier
- EFO_0003894
- Condition identifier
- MONDO_0005249
- Highest recorded phase
- 4
- Condition identifier
- MONDO_0011438
- Highest recorded phase
- 1
- Warning
- Black Box Warning
- Effect
- gastrointestinal toxicity
- Warning
- Black Box Warning
- Effect
- infectious disease
- Warning
- Black Box Warning
- Effect
- gastrointestinal toxicity
- Country
- United States
- Warning
- Black Box Warning
- Effect
- infectious disease
- Country
- United States
- Event
- acute generalised exanthematous pustulosis
- Reports
- 52
- Reporting signal score
- 103.728
- Event
- clostridium difficile colitis
- Reports
- 30
- Reporting signal score
- 45.6839
- Event
- drug hypersensitivity
- Reports
- 1,579
- Reporting signal score
- 4,222.71
- Event
- fall
- Reports
- 5
- Reporting signal score
- 43.9233
- Event
- fatigue
- Reports
- 26
- Reporting signal score
- 57.0786
- Event
- pruritus
- Reports
- 137
- Reporting signal score
- 52.3093
- Event
- pseudomembranous colitis
- Reports
- 25
- Reporting signal score
- 68.3936
- Event
- rash
- Reports
- 333
- Reporting signal score
- 222.657
- Event
- rash maculo-papular
- Reports
- 62
- Reporting signal score
- 80.9699
- Event
- toxic skin eruption
- Reports
- 46
- Reporting signal score
- 78.9748
- Event
- urticaria
- Reports
- 130
- Reporting signal score
- 80.0301
- NCT02099240
- NCT02593383
- Dose
- 150-300 mg
- Route
- Oral
- How often
- Every 6 hours
- At least 30 minutes before lying down
- Take with a full glass of water (6 to 8 ounces)
- Hydrogen bond acceptors
- 7
- Hydrogen bond donors
- 4
- Polar surface area
- 102.26
- Calculated partition coefficient (ALogP)
- 0.39
- Prodrug
- No
- Chirality
- Single enantiomer
- Inorganic
- No
- Rule-of-five violations
- 0
- Rotatable bonds
- 7
- Heavy atoms
- 28
- Molecular formula
- C18H34Cl2N2O5S
- Monoisotopic mass
- 460.1565488
- Natural product
- Yes
- 0009-0225
- 0009-0331
- 0009-0395
- 0904-5959
- 0904-7194
- 42571-250
- 42571-251
- 42571-252
- 50268-185
- 51407-373
- 51655-317
- 51655-710
- 51655-964
- 55700-761
- 60760-487
- 60760-827
- 60760-828
- 62135-764
- 62135-765
- 62135-766
- 63187-127
- 63187-141
- 63187-247
- 63304-692
- 63304-693
And 69 more, listed on the interactive page.
- Recorded assays
- 151
- Active assays
- 0
- Anti-Bacterial Agents
- Protein Synthesis Inhibitors
Related records
Trials (133)
- A Clinical Study Evaluating the Safety and Efficacy of IDP-110 in Patients With Acne Vulgaris
- A Clinical Study to Evaluate the Safety and Effectiveness of an Investigational Product Called CT Gel
- A Clinical Trial Evaluating the Safety and Efficacy of IDP-110 in Patients With Acne Vulgaris
- A Comparative Study of the Tolerability of Two Combination Therapies for the Treatment of Acne
- A Phase 4, Single-Blind, Randomized, Study to Compare the Tolerability and Efficacy of 0.1% Tazorac Cream When Used in Combination With Either Duac Gel or Acanya Gel for the Treatment of Facial Acne Vulgaris
- A Phase III Comparative Study of Dapsone / Trimethoprim and Clindamycin / Primaquine Versus Sulfamethoxazole / Trimethoprim in the Treatment of Mild-to-Moderate PCP in Patients With AIDS
- A Pilot Study of Oral Clindamycin and Pyrimethamine for the Treatment of Toxoplasmic Encephalitis in Patients With AIDS
- A Pilot, Multi-Center, Patient Preference Study Comparing Two Clindamycin/Benzoyl Peroxide Gels.
- A Randomized, Controlled Trial of the Effectiveness of Perioperative Antibiotics for Reduction of Burn Wound Bacterial Concentration Following Grafting
- A Study CLBG and Benzoyl Peroxide Gel 1%/5% to BenzaClin® Gel in the Treatment of Acne Vulgaris
- A Study Comparing Aczone® Plus Differin® Versus Duac® Plus Differin® in Patients With Severe Facial Acne
- A Study Comparing Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel to Duac® Topical Gel in the Treatment of Acne Vulgaris
- A Study Comparing Clindamycin and Benzoyl Peroxide Gel 1.2%/3.75% to Onexton™ Gel in the Treatment of Acne Vulgaris
- A Study to Compare the Efficacy and Safety of a Combination of Ketoconazole and Clindamycin Compared to Tetracycline/Amphotericin B Combination Cream for the Treatment of Bacterial Vaginosis and Vaginal Candidiasis (P08077)
- A Study to Evaluate the Efficacy and Safety of Adapalene-Clindamycin Combination Gel in the Treatment of Acne Vulgaris
- A Study to Evaluate Tolerability of Two Topical Drug Products in the Treatment of Facial Acne
- Adherence to Study Medication Compared to Generic Topical Clindamycin Plus Generic Topical Tretinoin in Subjects With Mild to Moderate Acne Vulgaris
- Adjunctive Clindamycin for Cellulitis: C4C Trial.
- Adjunctive Clindamycin for the Treatment of Skin and Soft Tissue Infections, a Randomized Controlled Trial
- Adjunctive Clindamycin Versus Linezolid for β-lactam Treated Patients With Invasive Group A Streptococcal Infections
Approved for (1)
In development for (2)
- Acne Phase 1
- Osteomyelitis Early phase 1